-
T Cell Subsets in Renal Transplant Rejection
-
HLA Typing with Matching of the Recipient and an Allograft Donor
-
Types of Transplant Rejection Based on the Time to Onset
-
Clinical Severity of Reaction in Food Allergy
-
Risk Factors for Severe Reaction in Peanut Allergy
-
Symptom Score of Verwimp et al for Cow's Milk Protein Intolerance in Infants
-
Grading Reaction Severity in Peanut and Nut Allergy
-
Recommendations of Bock et al for Reducing the Risk of a Food-Related Allergic Reaction in a School
-
Equations of Vanto et al for Predicting Tolerance to Milk By 4 Years of Age in an Infant with Cow's Milk Hypersensitivity
-
Conditions That Can Be Confused with a Food Allergy
-
Cross Reactions Between Fruits and Vegetables with Airborne Pollens
-
Food Protein-Induced Enterocolitis Syndrome (FPIES) in Infants and Young Children
-
Inhalation of a Food Allergen
-
Risk Factors of Nowak-Wegrzyn et al for a Reaction During an Oral Food Challenge
-
When To and Not To Perform an Oral Food Challenge
-
Kiss-Induced Allergic Symptoms Associated with a Food Allergy
-
Clinical Findings Associated with Cow's Milk Allergy in an Infant
-
Pulmonary Disease Associated with Cow Milk Allergy in Infants (Heiner Syndrome, Cow Milk-Induced Pulmonary Hemosiderosis)
-
Pork-Cat Syndrome
-
Allergy to Galactose-[alpha]-1,3-Galactose (alpha Gal) and Allergy to Meat
-
Risk Factors for Hidden Food Allergens
-
Food Protein-Induced Enterocolitis Syndrome (FPIES) Associated with Rice
-
Clinical Findings of Elizur et al That Can Help to Identify an Infant Mislabelled As Having Cow Milk Allergy
-
Types of Cow Milk Allergy (CMA)
-
CSF-to-Serum Albumin Index and the Intactness of the Blood-Brain Barrier
-
CSF IgG-to-Albumin Ratio and CNS Production of Antibody
-
CSF-to-Serum IgG Index and CNS Production of Antibody
-
CSF IgG Index
-
CNS IgG Synthesis Rate
-
CSF Kappa and Lambda Free Light Chain (KFLC and LFLC) Indices
-
Criteria of Holmes et al for the Diagnosis of the Chronic Fatigue Immune Dysfunction Syndrome
-
Prognostic Factors of Hartz et al for Patients with the Chronic Fatigue Syndrome
-
Oxford Research Criteria for the Diagnosis of the Chronic Fatigue Syndrome
-
Criteria of Fukuda et al for Chronic Fatigue Syndrome (International Chronic Fatigue Syndrome Study Group)
-
Oxford Research Criteria for Post-Infectious Fatigue Syndrome (PIFS)
-
Ratio of Kappa-to-Lambda Light Chains in the Serum
-
Relative Staining of Kappa-to-Lambda Light Chains in Bone Marrow Biopsies
-
Criteria for Decreased Levels of Serum Immunoglobulin A (IgA Deficiency States)
-
Differential Diagnosis of Marked Hypergammaglobulinemia
-
Patterns of Immunofluorescent Antinuclear Antibodies (ANA)
-
Clinical Indications for Measurement of Anti-Neutrophil Cytoplasmic Antibodies (ANCA)
-
Conditions Associated with a Positive Assay for Rheumatoid Factor (RF)
-
1982 ACR Criteria for the Diagnosis of Systemic Lupus Erythematosus
-
Systemic Lupus Erythematosus Disease Activity Index (SLEDAI)
-
SLICC/ACR Damage Index for Systemic Lupus Erythematosus
-
The Lupus Activity Criteria Count (LACC)
-
Systemic Lupus Activity Measure (SLAM)
-
Flare Severity Score of Lockshin et al for Patients with Systemic Lupus Erythematosus
-
The Activity Index of le Riche for Systemic Lupus Erythematosus
-
The Neonatal Lupus Syndromes
-
The SELENA Flare Tool
-
Diagnostic Features of Drug-Induced Lupus Erythematosus (DIL)
-
Risk Factors for Drug-Induced Lupus Erythematosus
-
Management of a Patient with Drug-Induced Lupus Erythematosus
-
The European Consensus Lupus Activity Measurement (ECLAM)
-
Model of Ward et al for Predicting In-Hospital Mortality for a Patient with Systemic Lupus Erythematosus (SLE)
-
Clinical Features of Protein-Losing Enteropathy in a Patient with Systemic Lupus Erythematosus
-
Criteria of Zeitouni et al for Rowell's Syndrome (Lupus Erythematosus with Erythema multiforme-like Skin Lesions)
-
Total Activity Score of the Cutaneous LE Disease Area and Severity Index (CLASI)
-
Total Damage Score of the Cutaneous LE Disease Area and Severity Index (CLASI)
-
British Isles Lupus Assessment Group (BILAG) Index
-
The Revised British Isles Lupus Assessment Group (BILAG) Index 2004
-
Risk Factors of Yip et al for Left Ventricular Systolic Dysfunction in a Patient with Systemic Lupus Erythematosus (SLE)
-
University College Hospital (UCH) and Middlesex Score for Disease Activity in Systemic Lupus Erythematosus (SLE)
-
Grading Organ Involvement for the University College Hospital (UCH) and Middlesex Score for Disease Activity in Systemic Lupus Erythematosus (SLE)
-
The BILAG Categories for General Non-Specific Manifestations of SLE
-
The BILAG Categories for Mucocutaneous Manifestations of SLE
-
The BILAG Categories for Musculoskeletal Manifestations of SLE
-
The BILAG Categories for Cardiovascular and Respiratory Manifestations of SLE
-
The BILAG Categories for Vasculitis Manifestations of SLE
-
The BILAG Categories for Hematological Manifestations of SLE
-
The BILAG Categories for Nervous System Manifestations of SLE Identified on the Initial Assessment
-
The BILAG Categories for Nervous System Manifestations of SLE Identified on a Followup Assessment
-
The BILAG Categories for Renal Manifestations of SLE Identified on the Initial Assessment
-
The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Proteinuria
-
The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Hypertension and Renal Function
-
The BILAG Categories for Renal Manifestations of SLE on a Followup Assessment: Final Diagnosis
-
Risk Factors of Karassa et al for Central Nervous System (CNS) Involvement in a Patient with Systemic Lupus Erythematosus
-
ANA Negative Systemic Lupus Erythematosus (SLE)
-
Psychosis and Visceral Involvement in a Patient with Systemic Lupus Erythematosus and Anti-Ribosomal P Protein Antibody
-
Clinical Features of Mucosal Lupus Erythematosus
-
Clinical Features of Chilblain Lupus Erythematosus Hutchinson
-
Alopecia and Other Changes in Hair Associated with Lupus Erythematosus
-
Use of the BILAG Index to Define a Lupus Flare
-
Severity of CNS Changes on Cranial MRI in a Patient Systemic Lupus Erythematosus
-
Neuropsychiatric Syndromes in Systemic Lupus Erythematosus (SLE)
-
Risk Factors of Tomietto et al for Cognitive Impairment in Systemic Lupus Erythematosus (SLE)
-
Risk Factors of Mikdashi et al for Epilepsy in a Patient with Systemic Lupus Erythematosus (SLE)
-
Shrinking Lungs Syndrome (SLS) in a Patient with Systemic Lupus Erythematosus
-
Acute Reversible Hypoxia Syndrome in a Patient with Systemic Lupus Erythematosus
-
Clinical Features of Acute Lupus Pneumonitis
-
Lupus Demylinating Syndrome (Lupoid Sclerosis)
-
Risk Factors of Mikdashi et al for Ischemic Stroke in a Patient with Systemic Lupus Erythematosus
-
Rhupus Syndrome
-
Modified Classification of Saketkoo and Quinet for Lupus Arthropathy
-
Index of van Vugt et al for Jaccoud’s Arthropathy
-
Flow Diagram of van Vugt et al for Classifying a Patient with SLE and a Deforming Arthropathy
-
Clinical and Laboratory Features of a Patient with Systemic Lupus Erythematosus (SLE) and Biopsy-Proven Myositis
-
American Rheumatism Association (ARA) Criteria for the Diagnosis of Rheumatoid Arthritis
-
Classification Tree for Diagnosis of Rheumatoid Arthritis
-
The Rheumatoid Arthritis Disease Activity Index (RADAI)
-
Criteria of Pinals et al for Complete Clinical Remission in Rheumatoid Arthritis
-
Felty's Syndrome
-
Issues Impacting the Decision to Use Second Line Drugs in the Management of a Patient with Rheumatoid Arthritis
-
Criteria of Steinbrocker et al for Therapeutic Response in a Patient with Rheumatoid Arthritis
-
The Index of Mallya and Mace for Disease Activity in Rheumatoid Arthritis
-
Rheumatoid Arthritis Disease Activity Scores (DAS) of van der Heijde et al
-
Disease Activity Index of Scott for Evaluating Improvement Following Treatment of Rheumatoid Arthritis
-
Algorithm of Fehring and Brooks for Treatment of a Patient with Rheumatoid Arthritis and Neck Pain
-
Sakaguchi-Kauppi Method to Screen for Vertical Atlantoaxial Dislocation in a Patient with Rheumatoid Arthritis
-
The PIP Joint Synovitis Score for a Patient with Rheumatoid Arthritis
-
The Stoke Index of Davis et al for Measuring Disease Activity in a Patient with Rheumatoid Arthritis
-
Algorithm of Brennan et al for Predicting the Risk of Developing Radiological Erosions in a Patient with Early Rheumatoid Arthritis
-
Articular Index (AI) Score of Ritchie et al for a Patient with Rheumatoid Arthritis
-
Clinical Practice Decision Tree of the French Society of Rheumatology for the First Disease Modifying Antirheumatic Drug in Very Early Rheumatoid Arthritis
-
Decision Tree of Nell et al for Identifying the Risk of Developing Erosive Disease in a Patient with Early Arthritis
-
Disease Activity Score of Prevoo et al for Rheumatoid Arthritis Based on Separate 28 Joint Counts for Tender and Swollen Joints (DAS28, DAS28T+S, DAS28 ESR)
-
The Index of Lansbury and Haut for Quantifying the Total Joint Inflammation and Deformity in a Patient with Rheumatoid Arthritis
-
Grades of Larsen for Radiographic Changes in Rheumatoid Arthritis
-
American College of Rheumatology Criteria for Improvement in Rheumatoid Arthritis Based on a 20 Percent Improvement in the Core Data Set (ACR20)
-
EULAR Therapeutic Response Criteria in a Patient with Rheumatoid Arthritis Based on the Change in DAS28 or DAS Scores
-
Model of Drossaers-Bakker et al for Identifying a Patient at Risk for Severe Rheumatoid Arthritis Within 12 Years Based on Baseline Parameters
-
Classification of Pellicci et al for Rheumatoid Arthritis Affecting the Cervical Spine
-
Indications of Bouchaud-Chabot and Liote for Surgery in a Patient with Rheumatoid Arthritis Involving the Cervical Spine
-
2009 ACR/EULAR Criteria for Rheumatoid Arthritis
-
DAS28 Scores Using C-Reactive Protein (DAS28 CRP)
-
DAS Scores Using C-Reactive Protein (DAS CRP)
-
RAPID3 (Routine Assessment of Patient Index Data 3)
-
2010 American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) Classification Criteria for Rheumatoid Arthritis
-
Indications for Considering a Total Joint Arthroplasty in a Patient with Rheumatoid Arthritis
-
Semiquantitative Scales of Szkudlarek et al to Describe the Ultrasonographic Changes in Joints Affected by Rheumatoid Arthritis
-
Rheumatoid Meningitis
-
The Simplified Disease Activity Index (SDAI) and Clinical Disease Activity Index (CDAI) for a Patient with Rheumatoid Arthritis
-
American College of Rheumatology (ACR) and European League Against Rheumatism (EULAR) Criteria for Remission in Rheumatoid Arthritis for a Clinical Trial
-
7 Joint Ultrasound Score of Backhaus et al (German US7 Score) : Subscore for Erosions
-
7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Tenosynovitis and Paratendonitis
-
7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Synovitis Using Gray-Scale Ultrasound (GSUS)
-
7 Joint Ultrasound Score of Backhaus et al (German US7 Score): Subscore for Synovitis Using Power Doppler Ultrasound (PDUS)
-
Algorithm of Nam et al for Management of a Patient with Early Inflammatory Arthritis
-
American College of Rheumatology (ACR) Criteria for Polyarteritis Nodosa
-
Classification Tree for the Diagnosis of Polyarteritis Nodosa
-
Criteria of Ozen et al for Diagnosis of Polyarteritis Nodosa in Childhood
-
Criteria for Polyarteritis Nodosa from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Clinical Features of Polyarteritis Nodosa Associated with Viral Hepatitis B
-
Polyarteritis Nodosa in a Neonate Born to a Mother with Polyarteritis Nodosa
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Churg-Strauss Syndrome
-
Classification Tree for the Diagnosis of Churg-Strauss Syndrome
-
Criteria for Churg-Strauss Syndrome from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Clinical Features of Churg-Strauss Syndrome
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Wegener's Granulomatosis
-
Classification Tree for the Diagnosis of Wegener's Granulomatosis
-
Histologic Diagnosis of Wegener's Granulomatosis Based on Biopsy from the Head and Neck
-
Criteria for a Major Exacerbation of Wegener's Granulomatosis
-
Disease Activity Index for Wegener's Granulomatosis
-
Histopathologic Findings of Matsubara et al in a Nasal Biopsy from a Patient with Wegener's Granulomatosis
-
Criteria for Wegener's Granulomatosis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Prognostic Features for a Patient with Wegener's Granulomatosis
-
Prognostic Factors of Slot et al for a Patient with PR3-ANCA Associated Vasculitis with Renal Involvement
-
Clinical and Laboratory Findings Associated with Wegener's Granulomatosis
-
Criteria for Limited Wegener's Granulomatosis from the Wegener's Granulomatosis Etanercept Trial
-
ELK Classification of DeRemee et al for Wegener's Granulomatosis
-
Modified ELK Score of Reinhold-Keller et al for Describing the Extent of Wegener's Granulomatosis
-
Predictors of Kamali et al for Survival in a Patient with Wegener's Granulomatosis
-
Modified Birmingham Vasculitis Activity Score (BVAS) for Wegener's Granulomatosis
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Temporal (Giant Cell) Arteritis
-
Classification Tree for the Diagnosis of Temporal (Giant Cell) Arteritis
-
Criteria of Chuang et al for Polymyalgia Rheumatica
-
Criteria of Healey for Polymyalgia Rheumatica
-
Criteria for Large Vessel Vasculitis (Giant Cell vs Takayasu Arteritis) from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Criteria of Bird et al for Polymyalgia Rheumatica
-
Risk Factors of Larsson et al for Giant Cell Arteritis in Women
-
Algorithm of Shmerling for a Patient with Possible Temporal Arteritis
-
Risk Factors of Nesher et al for Cranial Ischemic Complications in a Patient with Giant Cell Arteritis
-
Clinical Features of Temporal (Giant Cell) Arteritis
-
Temporal Artery Biopsy Formula of Younge et al
-
Reasons for a False Negative Temporal Artery Biopsy in a Patient with Giant Cell Arteritis
-
Algorithm of Hellman and Hunder for Using Color Doppler Ultrasonography in the Evaluation of a Patient Suspected of Having Giant Cell Arteritis
-
2012 EULAR/ACR Scoring Algorithm for Polymyalgia Rheumatica (PMR)
-
Patient Factors of Breuer et al Associated with the Diagnosis of Giant Cell Arteritis Following a Negative Temporal Artery Biopsy
-
Indications of Alberts and Mosen for Performing a Temporal Artery Biopsy Following Duplex Ultrasonography
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Hypersensitivity Vasculitis
-
Classification Tree for the Diagnosis of Hypersensitivity Vasculitis
-
Criteria for Cutaneous Leukocytoclastic Angiitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Henoch-Schonlein Purpura
-
Classification Tree for the Diagnosis of Henoch-Schonlein Purpura
-
Criteria for Henoch-Schonlein Purpura from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
American College of Rheumatology (ACR) Criteria for the Diagnosis of Takayasu Arteritis
-
Classification Tree for the Diagnosis of Takayasu Arteritis
-
Criteria of Ishikawa for the Diagnosis of Takayasu Arteritis
-
Criteria of Sharma et al for the Diagnosis of Takayasu Arteritis
-
Criteria of Kerr et al for Active Takayasu Arteritis
-
Criteria for the Diagnosis of Behcet’s Disease from the International Study Group for Behcet’s Disease
-
Diagnostic Criteria for Behcet’s Syndrome from the Behcet’s Disease Research Committee of Japan
-
Behcet's Disease Activity Index of Lawton et al
-
Mouth and Genital Ulcers with Inflamed Cartilage (MAGIC Syndrome)
-
Clinical and Laboratory Findings in Neuro-Behcet's Disease
-
Findings Suggesting a Poor Prognosis in a Patient with Neuro-Behcet's Disease
-
Criteria of Dilsen et al for the Skin Pathergy Test (SPT) in Behcet’s Disease
-
Pseudo-Behcet Syndrome
-
Disease Activity Index for Intestinal Behcet’s Disease (DAIBD) of Cheon et al
-
Monitoring the Change in the Disease Activity Index for Intestinal Behcet’s Disease (DAIBD) Over Time
-
Clinical Stage and Grade of Acute GVHD by Glucksberg et al
-
International Bone Marrow Transplant Registry (IBMTR) Severity Index for Grading Acute Graft versus Host Disease
-
Histopathologic Grading of Acute Graft versus Host Disease
-
Acute Graft versus Host Activity Index (aGVHDAI) of Leisenring et al
-
Prognostic Factor Score of Akpek et al for a Patient with Chronic Graft-versus-Host Disease (GVHD)
-
Indications of Irani et al for Requesting a Surgical Consult in a Patient with Severe Acute Gastrointestinal Graft-versus-Host Disease (GVHD)
-
Risk Factors of Jacobsohn et al for Overall Survival in a Child with Chronic Graft-versus-Host Disease (GVHD) Following Allogeneic Hematopoietic Stem Cell Transplant (HSCT)
-
Criteria for the Diagnosis of Sjogren's Syndrome
-
Histologic Grading of a Labial Salivary Gland Biopsy in Patients with Sjogren's Syndrome
-
Criteria of Fox et al for Sjogren's Syndrome (La Jolla or California Criteria)
-
Criteria of Homma et al for Sjogren's Syndrome (Japanese Ministry of Health and Welfare)
-
Criteria of Segerberg-Konttinen et al for Sjogren's Syndrome
-
Criteria of Skopouli et al for Sjogren's Syndrome (Greek Criteria)
-
Criteria of Manthorpe et al for Sjogren's Syndrome (Copenhagen Criteria)
-
Criteria of Vitali et al for Sjogren's Syndrome (Preliminary European Criteria)
-
Classification Tree of Vitali et al for Primary Sjogren's Syndrome
-
Exclusion Conditions in the Diagnosis of Sjogren's Syndrome
-
Sjogren's Syndrome Disease Damage Index (SSDDI)
-
Sjogren's Syndrome Disease Activity Index (SSDAI)
-
Ultrasonographic Score of Hocevar et al for the Major Salivary Glands in Primary Sjogren's Syndrome
-
Classification of Makula et al for Ultrasonographic Changes in the Parotid Gland Associated with Primary Sjogren's Syndrome
-
Classification of Niemela et al for Ultrasonographic Changes in Salivary Glands Associated with Primary Sjogren's Syndrome
-
Secondary Sjogren's Syndrome Associated with Hepatitis C Virus (HCV)
-
Criteria of the Sjogren’s International Collaborative Clinical Alliance (SICCA) Research Groups for Sjogren’s Syndrome
-
Criteria of McAdam et al for the Diagnosis of Relapsing Polychondritis
-
Systemic Disorders Associated with Relapsing Polychondritis
-
Birmingham Vasculitis Activity Score (BVAS)
-
Vasculitis Damage Index (VDI)
-
Systemic Necrotizing Vasculitis Damage Index (SNVDI)
-
The French Five Factor Score (FFS)
-
Criteria of Shionoya for Thromboangiitis Obliterans (TAO, Buerger's Disease)
-
Vasculitis Associated with Cocaine or Amphetamine Abuse, Including Pseudo-Wegener's Granulomatosis
-
Differential Diagnosis of a Pulmonary-Renal Vasculitic Syndrome
-
Clinical Features of Degos Syndrome (Malignant Atrophic Papulosis, Lymphocytic Arteriolitis)
-
Clinical and Laboratory Features of Schnitzler's Syndrome
-
Criteria of Lipsker et al for Schnitzler's Syndrome
-
Criteria of Scott and Bacon for Systemic Rheumatoid Vasculitis
-
Differential Diagnosis of Small Vessel Vasculitis
-
Clinical Classification of the European Vasculitis Study Group (EVSG) for the Disease Severity of an ANCA-Associated Vasculitis
-
Causes of Pseudovasculitis
-
Criteria for Reiter's Syndrome
-
Screening Questionnaire for Ankylosing Spondylitis
-
Rome Criteria for Ankylosing Spondylitis
-
New York Criteria for Ankylosing Spondylitis
-
Modified New York Criteria for Ankylosing Spondylitis
-
Criteria of Amor et al for Spondylarthropathy
-
The European Spondylarthropathy Study Group (ESSG) Criteria for Spondylarthropathy
-
Prediction of Longterm Outcome in Spondyloarthropathy Using the Score of Amor et al
-
Disease Activity Index for Reactive Arthritis (DAREA)
-
Criteria of Creemers et al for Active Disease in Ankylosing Spondylitis
-
Ankylosing Spondylitis Disease Activity Score (AS-DAS) of Creemers et al
-
The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI)
-
Articular Index of Dougados et al for Patients with Ankylosing Spondylitis
-
Criteria of the Ankylosing Spondylitis Working Group for Clinical Remission
-
Criteria of the Ankylosing Spondylitis Working Group for Clinical Response to Therapy
-
Bath Ankylosing Spondylitis Functional Index (BASFI)
-
Mander Enthesis Index (MEI) in Ankylosing Spondylitis
-
Reduced Mander Enthesis Index of Heuft-Dorenbosch et al for Ankylosing Spondylitis
-
Concise Enthesis Index of Heuft-Dorenbosch et al for Ankylosing Spondylitis (Maastrich Ankylosing Spondylitis Enthesitis Score, MASES)
-
Criteria of Sieper and Braun for Reactive Arthritis
-
Criteria of the Deutschen Gesellschaft fur Rheumatologie for Reactive Arthritis
-
Stoke Ankylosing Spondylitis Spine Score (SASSS)
-
Bath Ankylosing Spondylitis Radiology Index (BASRI, BASRI-s)
-
MRI Chronicity Index and Activity Index of Bollow et al in a Patient with Sacroiliitis
-
Bath Ankylosing Spondylitis Metrology Index (BASMI)
-
Modified Schober Index of Macrae and Wright for Measuring Back Flexion
-
Early Diagnostic Criteria of Mau et al for Ankylosing Spondylitis
-
ILAR (International League of Associations for Rheumatology) Criteria for Juvenile Enthesitis-Related Arthritis
-
Prognostic Factors of Leirisalo-Repo for Reactive Arthritis and the Spondyloarthropathies
-
Edmonton Ankylosing Spondylitis Metrology Index (EDASMI)
-
Clinical Features of Arthritis Associated with Ulcerative Colitis
-
Criteria of Rudwaleit et al for Inflammatory Back Pain in a Young to Middle-Aged Adult with Chronic Back Pain
-
ASAS Criteria for Inflammatory Back Pain in Patients with Chronic Back Pain
-
ASAS Classification Criteria for Axial Spondyloarthritis
-
Ankylosing Spondylitis Disease Activity Score (ASDAS) of the Assessment in SpondylArthritis international Society (ASAS)
-
Berlin MRI Spine Score for Ankylosing Spondylitis (AS)
-
Reactive Arthritis Associated with Tuberculosis (Tuberculous Rheumatism, Poncet’s Disease)
-
Risk Factors of Poddubnyy and Sieper for Radiographic Progression in Anklyosing Spondylitis and Axial Spondyloarthritis
-
ARA Scleroderma Criteria Cooperative Study Preliminary Clinical Criteria for Systemic Sclerosis
-
Hidebinding/Tethering Skin Score of Furst et al for Scleroderma
-
Rodnan Score for Progressive Systemic Sclerosis
-
Modified Rodnan Skin Score in Scleroderma Using 17 Sites
-
Modified Rodnan Skin Score in Scleroderma Using 5 Sites
-
Organ System Indices of Furst et al in Systemic Sclerosis
-
Kahaleh Skin Score in Scleroderma
-
Predictors of Steen et al for Scleroderma Renal Crisis
-
Risk Model of Bryan et al for 5 Year Survival in a Patient with Scleroderma
-
Criteria of Valentini et al (European Scleroderma Study Group) for Activity of Systemic Sclerosis
-
Criteria of Valentini et al (European Scleroderma Study Group) for Activity of Diffuse and Limited Systemic Sclerosis
-
Criteria of Steen et al for Scleroderma Renal Crisis
-
Classification of Maricq for Changes Seen in the Fingernail Capillaries of a Patient with Scleroderma
-
Nailfold Capillary Microscopic Profiles of Joyal et al in a Patient with Systemic Sclerosis
-
Criteria of LeRoy and Medsger for Limited Forms of Systemic Sclerosis (lSSc)
-
Criteria of LeRoy and Medsger for Limited Cutaneous (lcSSc, CREST Syndrome) or Diffuse Cutaneous Systemic Sclerosis (dcSSc)
-
Clinical Features of Occupation-Related Scleroderma
-
Criteria of Lally et al for Rapidly (Fulminant) Progressive Systemic Sclerosis
-
Clinical Findings Associated with Involvement of the Esophagus or Stomach in Systemic Sclerosis
-
Presenting Symptoms of Progressive Systemic Sclerosis
-
Criteria of the PRES/ACR/EULAR for the Diagnosis of Juvenile Systemic Sclerosis
-
Osteolysis with Bone Resorption in Systemic Sclerosis
-
Prognostic Factors of Martini et al for a Patient with Juvenile Systemic Sclerosis
-
Diagnostic Clues of Hudson for the Diagnosis of Systemic Sclerosis
-
Drug-Induced Scleroderma
-
Lung Severity Scale of Medsger et al for a Patient with Systemic Sclerosis
-
Cardiac and Vascular Severity Scales of Medsger et al for a Patient with Systemic Sclerosis
-
General and Skin Severity Scales of Medsger et al for a Patient with Systemic Sclerosis
-
Renal and Gastrointestinal Scales of Medsger et al for a Patient with Systemic Sclerosis
-
Joint and Muscle Scales of Medsger et al for a Patient with Systemic Sclerosis
-
Prognostic Factors of Hachulla et al for a Patient with Systemic Sclerosis
-
Criteria of Penn et al for Scleroderma Renal Crisis
-
Factors Associated with a Poor Prognosis for a Patient with Scleroderma Renal Crisis
-
Scleroderma Associated with Silica Exposure (Erasmus Syndrome)
-
Conditions in the Differential Diagnosis of Scleroderma (Scleroderma-Like Fibrosing Skin Disorders)
-
Classification Criteria of Tanimoto et al for Polymyositis and Dermatomyositis
-
Childhood Myositis Assessment Scale (CMAS) for the Evaluation of Muscle Function in Juvenile Idiopathic Inflammatory Myopathy
-
Prognostic Factors of Benbassat et al for a Patient with Polymyositis or Dermatomyositis
-
Criteria of Bohan and Peter for the Diagnosis of Polymyositis and Dermatomyositis
-
Overlap Syndrome in a Patient with Dermatomyositis
-
Criteria of Marie et al for Remission of Polymyositis or Dermatomyositis
-
Prognostic Factors of Marie et al for a Patient with Polymyositis or Dermatomyositis
-
Prognostic Factors of Maugars et al for a Patient with Dermatomyositis or Polymyositis
-
Risk Factors of Chen et al for Underlying Malignancy in a Patient with Dermatomyositis or Polymyositis
-
Dermatomyositis Sine Myositis
-
Diagnostic Criteria for Sporadic Inclusion Body Myositis
-
Staging the Airway Risk in a Patient with Angioedema
-
Triage Algorithm for a Patient with Angioedema of the Head and Neck
-
Types of Angioneurotic Edema
-
Risk Factors of Kostis et al for Enalapril-Induced Angioedema
-
Classification of Kostis et al for the Severity of Angioedema Based on Treatment Intensity
-
Criteria of Agostini et al for the Diagnosis of Angioedema Associated with a Deficiency of C1-Inhibitor
-
Criteria of Agostoni et al for Determining the Severity of Hereditary Angioedema
-
Angioedema Associated with Estrogen Excess
-
Clinical Features of Gleich's Syndrome (Episodic Angioedema with Eosinophilia)
-
Conditions That May Be Confused with Angioedema
-
Persistent, Nonepisodic Angioedema with Eosinophilia of Chikama et al
-
Nodules, Eosinophilia, Rheumatism, Dermatitis and Swelling (NERDS)
-
Thymidine Incorporation by Lymphocytes and the Stimulation Index (SI)
-
Lymphocyte Cytotoxicity (LCT) Assay for Detecting Antibodies to HLA Antigens
-
Clinical Classification of Osserman and Genkins for Myasthenia Gravis
-
Clinical Crisis in Patients with Myasthenia Gravis
-
Predictors of Favorable Response to Thymectomy in Patients with Myasthenia Gravis
-
Prognostic Factors of Tellez-Zenteno et al in Patients with Myasthenia Gravis Following Thymectomy
-
Clinical Distinction of Myasthenia Gravis from Lambert-Eaton Myasthenic Syndrome
-
Clinical Classification of the Myasthenia Gravis Foundation of America (MGFA) for Myasthenia Gravis
-
Quantitative Score (QMG) for Disease Severity of the Myasthenia Gravis Foundation of America (MGFA)
-
Clinical Score of Besinger et al for a Patient with Myasthenia Gravis
-
Ice Pack Test for Evaluating a Patient with Ptosis
-
Red Flags of Spillane et al for an Imminent Myasthenic Crisis
-
Clinical Features of the Stiff Man Syndrome
-
Paraneoplastic Stiff Man Syndrome
-
Criteria of Brown and Marsden for the Stiff Man Plus Syndromes
-
Progressive Encephalomyelitis with Rigidity
-
Jerking Stiff Man Syndrome
-
Stiff Limb Syndrome
-
Screening Questionnaire for Latex Allergy
-
Risk Factors for a Person Having a Latex Allergy
-
Clinical Features of Latex Allergy in an Infant
-
Bronchoconstriction and Asthma Associated with Latex Allergy
-
Healthcare Equipment and Materials That May Contain Natural Rubber Latex (NRL)
-
Latex-Fruit Syndrome
-
Allergic Reactions to a Latex Condom
-
Criteria of Bennett for the Diagnosis of Psoriatic Arthritis
-
Risk Factors of Gladman et al for Mortality in Patients with Psoriatic Arthritis
-
Classification of Moll and Wright for Psoriatic Arthritis
-
Risk Factors of Gladman et al for Identifying a Patient at Diagnosis of Psoriatic Arthritis Who Is at Risk for Disease Progression
-
Tool of Helliwell et al for Evaluating Dactylitis in a Patient with Psoriatic Arthritis
-
Criteria of Southwood et al for the Diagnosis of Juvenile Psoriatic Arthritis (Vancouver Criteria)
-
Criteria for the Diagnosis of Psoriatic Arthritis of the CASPAR Investigators
-
Criteria of Vasey and Espinoza for Psoriatic Arthritis
-
Modified Criteria of McGonagle et al for the Diagnosis of Psoriatic Arthritis
-
Criteria of Fournie et al for Psoriatic Arthritis
-
ILAR (International League of Assocations for Rheumatology) Criteria for Juvenile Psoriatic Arthritis
-
Score of Wassenberg et al for Radiographic Changes in a Patient with Psoriatic Arthritis
-
Classification of Disease Severity in Psoriatic Arthritis Based on Therapy and Disability
-
Psoriatic Arthritis Response Criteria of Clegg et al (PsARC)
-
Allergic Rhinitis Severity Score of Lunn et al
-
Score for Allergic Rhinitis (SFAR) of Annesi-Maesano et al
-
Allergic Rhinitis Severity Score of Berges-Gimeno et al
-
Classification of Bousquet et al for Allergic Rhinitis
-
Total Nasal Symptom Score (TNSS), Cough Score and Overall Symptom Score of Gawchik et al for a Patient with Allergic Rhinitis
-
Indications for Referring a Patient with Allergic Rhinitis to a Specialist
-
Model of Visser et al for Early Prediction of Outcome in Patients with Arthritis
-
Synovialitis Score of Krenn et al for Grading Histologic Features of Chronic Synovitis
-
Tool of Len et al for Identifying a Pediatric Patient with Chronic Arthropathy Who Should Be Referred to a Rheumatologist
-
Prediction Rule of van der Helm-van Mil et al for Evaluating a Patient with a Recent Onset of Undifferentiated Arthritis
-
Clinical Features of Parvovirus B19-Associated Arthropathy
-
Relapsing Seronegative Symmetric Synovitis with Pitting Edema (RS3PE)
-
Steroid Pseudorheumatism (Arthralgias and Myalgias Associated with Steroid Withdrawal)
-
Arthritis Associated with Intestinal Bypass for Morbid Obesity (Intestinal Bypass Arthritis)
-
Risk Factors of Gonzalez-Lopez et al for Subsequent Development of a Connective Tissue Disorder in a Patient with Palindromic Rheumatism
-
Leprosy Presenting as an Autoimmune or Rheumatic Disorder
-
Food-Induced Allergic Arthritis
-
Dialysis-Related Amyloid Arthropathy (Beta2-Microglobulin Amyloid Arthropathy)
-
Septic Focus Syndrome
-
Early Persistent Inflammatory Synovitis Assessment (EPISA) Score of El Miedany et al
-
Clinical Findings Associated with Viral Hepatitis C-Associated Arthropathy
-
Differential Diagnosis of Recurrent or Relapsing Arthritis
-
Celiac Disease Arthropathy (Arthritis of Celiac Disease)
-
Evaluation of the Immune Status in a Patient With Bacterial Meningitis or Invasive Bacterial Infection
-
Clinical Features of the X-Linked Hyper-IgM Syndrome
-
Clinical Features of the Wiskott-Aldrich Syndrome (WAS)
-
Clinical Features of Hyper-IgE Syndrome (HIES, Job Syndrome)
-
Clinical Features of TAP Deficiency Syndrome (Type 1 BLS)
-
Clinical Features of Selective IgA Deficiency (IgAD)
-
Drug-Induced IgA Deficiency
-
Algorithm of Snowden et al for Evaluating a Patient with Rheumatoid Arthritis and a Gold-Induced Immunoglobulin Deficiency
-
When to Screen a Patient for a Primary Antibody Deficiency
-
When to Suspect Autosomal Recessive Agammaglobulinemia (ARA)
-
Drug-Induced Hypogammaglobulinemia
-
Transient Hypogammaglobulinemia of Infancy (THI)
-
Common Variable Immunodeficiency (CVID)
-
Clinical and Laboratory Features of Agammaglobulinemia
-
Causes of Acquired Hypogammaglobulinemia
-
Specific Antibody Deficiency (SAD) and Poor Response to Polysaccharide Vaccines
-
Clinical Findings in an Infant with Omenn's Syndrome
-
Clinical Features of X-Linked Severe Combined Immunodeficiency (SCID)
-
Clinical Features of Severe Combined Immunodeficiency (SCID) Associated with Adenosine Deaminase (ADA) Deficiency
-
Lymphocyte Phenotypes Associated with Various Combined Immunodeficiencies
-
Clinical Features of ZAP70-Related Severe Combined Immunodeficiency (SCID)
-
Monocytopenia Immunodeficiency Syndrome (MonoMAC) with Bone Marrow Failure
-
The 10 Warning Signs for Primary Immunodeficiency in Children of the Jeffrey Modell Foundation Medical Advisory Board
-
Warning Signs of Subbarayan et al for Primary Immunodeficiency Disease in Children
-
Severe Combined Immunodeficiency (SCID) Associated with CD3 delta Deficiency Involving T Lymphocytes
-
Predisposition to Infection Associated with Anticytokine Autoantibodies
-
When to Suspect the Presence of an Anticytokine Autoantibody
-
Score of Agarwal and Cunningham-Rundles for Management of a Patient with Hypogammaglobulinemia
-
Solar Urticaria
-
Aquagenic Urticaria and Aquagenic Pruritus
-
Cholinergic Urticaria (Generalized Heat-Induced Urticaria)
-
Dermographism (Dermatographism)
-
Classification of Fukunaga et al for Cholinergic Urticaria Based on Autologous Skin Testing
-
Separating a Significant Cold Agglutinin from a Laboratory Annoyance
-
Autoimmune Hemolytic Disease Associated with a Mature Teratoma or Other Ovarian Tumor
-
Paroxysmal Cold Hemoglobinuria (PCH, Donath Landsteiner Antibody-Related Hemolysis)
-
Indications for a Patient to Carry an Epinephrine (Adrenaline) Auto-Injector
-
Grades of Laxenaire for the Severity of an Anaphylactoid Reaction
-
Grading System of Brown for a Generalized Hypersensitivity Reaction
-
Risk Factors of Brown for Hypoxia in a Patient with a Generalized Hypersensitivity Reaction
-
Risk Factors of Brown for Hypotension in a Patient with a Generalized Hypersensitivity Reaction
-
Impact of Beta-Adrenergic Blocking Agents on a Patient with Anaphylaxis
-
Criteria of Sampson et al for Anaphylaxis
-
Grading Scheme of Ring and Messmer for Anaphylactic Symptoms
-
Nitritoid Reaction Following Gold Salt (Sodium Aurothiomalate) Therapy
-
Biphasic Anaphylactic Event
-
Serum Tryptase Activity
-
Classification of Montgomery et al for an Allergic Reaction to Isosulfan Blue Dye During Lymphatic Mapping
-
Cytokine Release Syndrome (CRS)
-
Clinical Features Associated with Interleukin-6 (IL-6, Interleukin-6 Syndrome)
-
Clinical Features of the Jarisch-Herxheimer Reaction
-
Infections Associated with a Jarisch-Herxheimer Reaction
-
Hereditary Defects in the Interferon-gamma and Interleukin-12 Pathway (Hereditary Susceptibility to Mycobacteria and Intracellular Pathogens)
-
Clinical Features of a Systemic Allergic Contact Dermatitis Reaction
-
Systemic Allergic Contact Dermatitis with a Bathing Trunk Distribution (Baboon Syndrome)
-
Grading Scale of Williams et al for Uroshiol Contact Dermatitis Following Exposure to Poison Ivy or Poison Oak
-
Clinical Features of Metal Sensitivity in a Patient with an Orthopedic Implant
-
Clinical Features of Mercury Sensitivity Associated with Dental Amalgam
-
Clinical Features of Nickel Sensitivity
-
Contact Allergic Reactions Following Exposure to Smoke from Burning Poison Ivy or Poison Oak
-
Contact Allergic Dermatitis to Lacquer (Sap of the Rhus Tree)
-
Systemic Allergic Dermatitis Following Oral Intake of Urushiol from the Rhus Tree as an Herbal Medicine
-
Contact Allergic Dermatitis to Mango
-
Contact Allergic Dermatitis to the Fruit of the Ginkgo Tree
-
Contact Allergy to Polyvinylpyrrolidone, Including Povidone-Iodine
-
Allergic Contact Sensitivity to Fiberglass (Fiberglass Dermatitis)
-
Oral Allergy Syndrome (OAS, Mucosal Contact Urticaria, Food Contact Hypersensitivity Syndrome)
-
Hypersensitivity Reaction to a Ventriculoperitoneal Shunt
-
Phytodermatitis Associated with Metopium toxiferum (Poison Wood, Poison Bark)
-
Phytodermatitis Associated with Parthenium Species
-
Kimura's Disease
-
Types of Brouet et al for Cryoglobulins
-
Clinical Findings in a Patient with Cryoglobulinemia
-
Reasons for Failure to Detect a Cryoglobulin
-
Clinical Findings in a Patient with Cryofibrinogen
-
Criteria for Essential Cryoglobulinemic Vasculitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Cryocrit
-
Criteria of Roccatello et al for Response to Therapy for a Patient with Cryoglobulinemia
-
Cryogelation Associated with Waldenstrom's Macroglobulinemia
-
Clinical Features of Goodpasture's Disease
-
Differential Diagnosis of Goodpasture's Syndrome
-
Risk Factors for Exacerbation of Goodpasture's Disease
-
Prognostic Factors of Levy et al for a Patient with Goodpasture's Disease
-
Clinical Features of the Autoimmune Lymphoproliferative Syndrome (ALPS)
-
Lofgren's Syndrome
-
Clinical Features Associated with an Acute vs Chronic Course in Systemic Sarcoidosis
-
Indications for Oral Corticosteroid Therapy in a Patient with Sarcoidosis
-
Criteria of Mana for Disease Activity in Sarcoidosis
-
Sarcoidosis Following Therapy with a Tumor Necrosis Factor (TNF) alpha Blocking Agent
-
Method of Judson for Assessing the Clinical Severity of Sarcoidosis
-
Acute Sarcoid Myositis (Acute Sarcoid Myopathy)
-
Blau Syndrome and NOD2 Mutations (Granulomatous Dermatitis, Uveitis and Arthritis)
-
Prognostic Factors of Neville et al for a Patient with Sarcoidosis
-
Reactivation of Sarcoidosis in a Patient Being Treated with Interferon
-
Late-Onset Sarcoidosis
-
Sarcoidosis Severity Scores of Wasfi et al
-
Clinical Severity Score of Gedalia et al for a Pediatric Patient with Sarcoidosis
-
Response Criteria of Gedalia et al in a Pediatric Patient with Sarcoidosis Treated with Methotrexate
-
Causes of a Misleading Allergen Skin Test
-
Skin Index of Ueno et al in Allergen Testing
-
Clinical Findings in Retroperitoneal Fibrosis
-
Causes of Retroperitoneal Fibrosis
-
Algorithm of Vaglio et al for the Management of a Patient with Retroperitoneal Fibrosis
-
Criteria of the Japanese Adult Still's Disease Research Committee for Adult Still's Disease
-
Criteria of Fautrel et al for Adult Onset Still's Disease (AOSD)
-
Criteria of Cush et al for Adult Onset Still's Disease
-
Clinical Findings of Efthimiou et al for Adult Onset Still's Disease
-
Risk Factors of Kong et al for Relapse in a Patient with Adult-Onset Still's Disease
-
Response Criteria of Fautrel et al to Therapy for Adult Still's Disease
-
Criteria of the Pediatric Rheumatology International Trials Organization (PRINTO) for Improvement in Juvenile Arthritis
-
ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Oligoarthritis
-
ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Polyarthritis
-
ILAR (International League of Associations for Rheumatology) Criteria for Idiopathic Juvenile Systemic Arthritis
-
ILAR (International League of Associations for Rheumatology) Criteria for "Other" Juvenile Arthritis
-
The Pediatric Escola Paulista de Medicina Range of Motion (EPM-ROM) Scale for Juvenile Rheumatoid Arthritis
-
American Rheumatism Association (ARA) Criteria for Juvenile Rheumatoid Arthritis
-
Risk of Malignancy in a Patient with Juvenile Arthritis Treated with a Tumor Necrosis Factor (TNF) alpha Inhibitor
-
Criteria of Wallace et al for Inactive Juvenile Idiopathic Arthritis (JIA)
-
Predictors of Schneider et al for Poor Functional Outcome in a Patient with Systemic-Onset Juvenile Rheumatoid Arthritis (JRA)
-
Criteria of Chamot et al for the SAPHO Syndrome
-
Criteria of Alarcon-Segovia and Villareal for the Diagnosis of Mixed Connective Tissue Disease
-
Criteria of Sharp for the Diagnosis of Mixed Connective Tissue Disease
-
Criteria of Kasukawa et al for the Diagnosis of Mixed Connective Tissue Disease
-
Discriminant Function of Ishikawa et al for Distinguishing Mixed Connective Tissue Disease from Progressive Systemic Sclerosis
-
Diagnostic Criteria of Scully et al for Familial Mediterranean Fever
-
Clinical Features of the Hyper-IgD Syndrome
-
Clinical Features of the TNF-Receptor Associated Periodic Syndrome (TRAP, Familial Hibernian Fever)
-
Criteria of Livneh et al for Complete or Incomplete Attacks in a Patient with Familial Mediterranean Fever
-
Criteria of Livneh et al for the Diagnosis of Familial Mediterranean Fever
-
Simplified Criteria of Livneh et al for the Diagnosis of Familial Mediterranean Fever
-
Clinical Features of the Familial Cold Autoinflammatory Syndrome (Familial Cold Urticaria)
-
Clinical Score of Settin et al for Familial Mediterranean Fever (FMF)
-
Indications for Using Colchicine in a Patient with Familial Mediterranean Fever
-
Clinical Features of Muckle-Wells Syndrome
-
Clinical Features of Chronic Infantile Neurological Cutaneous Articular Syndrome (CINCA Syndrome, NOMID)
-
Criteria for Microscopic Polyangiitis from the International Consensus Conference on the Nomenclature of Systemic Vasculitis (Chapel Hill Conference)
-
Differentiating Microscopic Polyangiitis from Polyarteritis Nodosa (PAN)
-
Clinical Features of Microscopic Polyangiitis
-
Criteria of Moore for Isolated Angiitis of the Central Nervous System
-
High Risk Profile of Benseler et al for a Child with Primary Central Nervous System Vasculitis
-
Criteria of Calabrese and Mallek for Primary Angiitis of the Central Nervous System (PACNS)
-
Benign Angiopathy of the Central Nervous System (Benign Angiitis of the Central Nervous System, BACNS)
-
Differential Diagnosis of Primary Angiitis of the Central Nervous System (PACNS)
-
Clinical Features of Cogan Syndrome
-
Risk of Exposure to Cockroach Allergens
-
Reducing Exposure to Dust Mite Allergens
-
Pancake Syndrome (Oral Mite Anaphylaxis)
-
Diseases That May Be Seen in a Patient with an Inherited Complement Deficiency
-
Body Fluid to Serum CH50 Ratio
-
Screening for a Complement Deficiency Using the CH50 and AH50
-
Criteria of Grotz et al for the Hypocomplementemic Urticarial Vasculitis Syndrome (HUVS, Anti-C1q Syndrome)
-
Clinical Features of Hereditary C3 Deficiency
-
SLE and Other Clinical Features of a Homozygous Deficiency in a Component of the Classical Complement Pathway
-
Risk for Neisseria Infections in a Patient Treated with Eculizumab
-
Preliminary Criteria of Mosca et al for Undifferentiated Connective Tissue Disease
-
Clinical and Laboratory Findings in a Patient with Undifferentiated Connective Tissue Disease
-
Findings in a Patient with Apparent Undifferentiated Connective Tissue Disease Who May Progress to Systemic Lupus Erythematosus (SLE)
-
Allergy to Ethylene Oxide
-
Clinical Clues of Naschitz for Occult Neoplasia in a Patient Presenting with a Rheumatic Disorder
-
Palmar Fasciitis and Polyarthritis Syndrome (PFPAS)
-
Paraneoplastic Autoimmune Multiorgan Syndrome (PAMS)
-
Minimum Workup of Mourad et al to Qualify for Fever of Unknown Origin
-
Algorithm of Mourad et al for Evaluating a Patient with Fever of Unknown Origin (FUO)
-
Conditions Associated with Fever of Unknown Origin (FUO)
-
Drugs That Can Cause Fever of Unknown Origin
-
Diagnostic Approach of Wagner et al to Identify Large Vessel Vasculitis in a Patient with Fever of Unknown Origin (FUO)
-
Criteria for the Diagnosis of a Fever of Unknown Origin (FUO)
-
Clinical Features of Serum Sickness
-
Drugs That Can Cause a Serum Sickness Like Reaction (SSLR)
-
Features of a Serum Sickness-Like Reaction
-
Classification of Gell and Coombs for Hypersensitivity Reactions
-
Contraindications to a Corticosteroid Injection
-
“Steroid Flare” Following an Intraarticular Injection of a Corticosteroid
-
Clinical Features of Chronic Recurrent Multifocal Osteomyelitis
-
Clinical Features of Chronic Nonbacterial Osteomyelitis (CNO)
-
Response to Therapy by a Patient with Chronic Recurrent Multifocal Osteomyelitis
-
Criteria of Masaki et al for IgG4-Positive Multi-Organ Lymphoproliferative Syndrome
-
Criteria of Yamamoto et al for Mikulicz's Disease with Involvement of Lacrimal and Salivary Glands
-
FDG PET-CT Scan for Evaluation of the Patient for IgG4-Related Plasmacytic Syndrome
-
Reducing Exposure to Pet Dander
-
Christmas Tree Syndrome (Christmas Tree Allergy)
-
Recommendations of Kurlandsky et al to Reduce Allergen Exposure Associated with a Coniferous Tree or Other Plant Decorations
-
Airborne Contact Dermatitis (ABCD)
-
Criteria of Umeki for Eosinophilic Pneumonia
-
Distinguishing Acute and Chronic Eosinophilic Pneumonia
-
Risk Factors of Scranton et al for a Biphasic Reaction Associated with Allergen Immunotherapy
-
Indications of Li et al for Allergen Immunotherapy in a Patient with Allergic Rhinitis and/or Allergic Asthma
-
Contraindications to Performing a Radioallergosorbent Test (RAST) to Detect Specific IgE Antibody
-
CAP System Scoring Scheme for a Radioallergosorbent Test (RAST)
-
Indications to Performing a Radioallergosorbent Test (RAST) to Detect Specific IgE Antibody
-
Clinical Features of Sclerosing Mediastinitis
-
Causes of the Abnormal Immunological Response in Sclerosing Mediastinitis
-
Prognostic Factors for a Patient with Sclerosing Mediastinitis
-
Clinical and Laboratory Features of the Antisynthetase Syndrome
-
Mechanic's Hands
-
Daily Urticaria Activity Score (UAS)
-
Using the Urticaria Activity Score (UAS) to Measure Response to Therapy for Chronic Urticaria
-
Symptom Score of Mlynek et al for a Patient with Chronic Urticaria
-
Scoring System of Kaplan et al for Urticaria Severity
-
Clinical and Laboratory Features of Chronic Autoimmune Urticaria
-
Autologous Serum Skin Test (ASST) in Chronic Idiopathic Urticaria
-
Criteria of Rodriguez for an Autoimmune Disorder
-
Moyamoya Syndrome in a Patient with Systemic Lupus Erythematosus (SLE)
-
Score of Crowson et al for Predicting the Risk of a Serious Infection in a Patient with Rheumatoid Arthritis (RA)
-
Additional Clinical and Laboratory Findings in Behcet’s Disease
-
Prognostic Score of Wingard et al for a Patient with Chronic Graft-versus-Host Disease After Bone Marrow Transplantation
-
Chronic Graft-versus-Host Disease (GVHD) Score of Lee et al.
-
Clinical Score of Jacobsohn et al for Grading Chronic Graft-versus-Host Disease (GVHD)
-
Criteria of Jacobsohn et al for Therapeutic Response in a Patient Being Treated for Chronic Graft-versus-Host Disease (GVHD)
-
Chronic GVHD Risk Score of Arora et al
-
Revised Classification Score of Cornec et al for Primary Sjogren's Syndrome (SS)
-
Ultrasound Inhomogeneity Score of Milic et al for a Patient with Sjogren's Syndrome
-
Paraneoplastic Scleroderma (Sclerodermiform Paraneoplastic Syndrome)
-
Disease Severity Score of La Torre et al for Juvenile Systemic Sclerosis
-
Predisposition to Fungal Infections Associated with Hereditary CARD9 Deficiency
-
Hereditary Conditions Associated with Impaired Interleukin-17 (IL-17) Function and Mucocutaneous Candidiasis
-
Definition of Micek et al for Immunosuppression
-
Tulip Fingers
-
Revised Criteria of Oliveira et al for Autoimmune Lymphoproliferative Syndrome (ALPS)
-
Nomenclature of Oliveira et al for Autoimmune Lymphoproliferative Syndrome (ALPS)
-
Recommended Initial Evaluation of a Patient with Sarcoidosis from the ATS/ERS/WASOG Statement
-
Clinical Features of Cellucci et al for a Child with Primary Angiitis of the Central Nervous System
-
Laboratory Findings of Cunha et al Associated with Tumor-Related Tumor Necrosis Factor
-
Naproxen Test (Naprosyn Test, NSAID Test) for Fever of Unknown Origin (FUO) Associated with an Underlying Cancer
-
Aseptic Abscess Syndrome (AAS)
-
Conditions Associated with the Splendore-Hoeppli Phenomenon
-
Histologic Features of the Splendore-Hoeppli Phenomenon
-
Criteria of Damiani and Levine for the Diagnosis of Relapsing Polychondritis
-
1997 ACR Update in the Criteria for the Diagnosis of Systemic Lupus Erythematosus
-
Clinical and Laboratory Findings of Lupus Enteritis
-
Intestinal Ischemia or Infarction in Rheumatoid Arthritis
-
Algorithm of Dammacco and Sansonno for Managing a Patient with HCV-Related Cryoglobulinemia
-
Predictors of van Dartel et al for Serious Infection in a Patient with Rheumatoid Arthritis Treated with Anti-Tumor Necrosis Factor (TNF alpha) Therapy
-
Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) (German)
-
Chronic Fatigue Syndrome Severity Score of Baraniuk et al
-
Criteria of the Institute of Medicine (IOM) for Myalgic Encephalitis/Chronic Fatigue Syndrome (ME/CFS, Systemic Exertional Intolerance Disease, SEID)
-
Risk Factors of Gustafsson et al for a First Cardiovascular Event in a Patient with Systemic Lupus Erythematosus
-
Risk Factors of Martinez-Martinez et al for Mortality in a Patient with Systemic Lupus Erythematosus (SLE) and Diffuse Alveolar Hemorrhage (DAH)
-
Rheumatoid Arthritis Observation of Biologic Therapy (RABBIT) Risk Scores for Serious Infection
-
Rheumatoid Nodulosis
-
Accelerated Nodulosis and Vasculitis Associated with Methotrexate Therapy in a Patient with Rheumatoid Arthritis
-
Simplified Model of de Punder et al for Predicting Joint Damage Progression in a Patient with Rheumatoid Arthitis
-
Extended Model of de Punder et al for Predicting Joint Damage Progression in a Patient with Rheumatoid Arthitis
-
Subglottic Stenosis and Other Manifestations of Wegener?s Granulomatosis (Granulomatosis with Polyangiitis) Involving the Laryngotracheobronchial Tree
-
Carotidynia in Takayasu Arteritis
-
Sjogren's Syndrome Associated with Sarcoidosis
-
Pseudo-Asthma Secondary to Relapsing Polychondritis
-
Criteria of Michet et al for the Diagnosis of Relapsing Polychondritis
-
Prognostic Factors of Michet et al for a Young Adult with Relapsing Polychondritis
-
Histologic Findings in Relapsing Polychondritis
-
Susac Syndrome
-
Lymphocytopenia Associated with a Lymphatic Malformation
-
Cytokine Storm Associated with TGN1412 (Anti-CD28 Monoclonal Antibody)
-
Indications of Shohat and Halpern for Evaluating a Patient for Familial Mediterranean Fever
-
Phenotypes of Familial Mediterranean Fever (FMF)
-
Klassifikationskriterien für die rheumatoide Arthritis der American Rheumatism Association 1987 (German)
-
Klassifikationskriterien für die rheumatoide Arthritis der American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) 2010 (German)
-
Kriterien der kompletten Remission für die rheumatoide Arthritis der American Rheumatism Association 1981 (German)
-
Risk Factors for Acute Myocardial Infarction in a Patient with Systemic Lupus Erythematosus
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Skin Lesions Activity
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Mucous Membrane Lesion Activity
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Alopecia Activity
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Skin Lesion Damage
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Alopecia Damage
-
Revised Cutaneous Lupus Erythematosus Disease Area and Severity Index (RCLASI): Total Activity and Damage Scores
-
Clues to Large Granular Lymphocytic Leukemia as the Cause of Rheumatoid Arthritis
-
Scoring Method of Zayat et al for Bone Erosions in Rheumatoid Arthritis Using Ultrasonography
-
Flares in Rheumatoid Arthritis (RA)
-
Overall Status of Rheumatoid Arthritis (OSRA) of Symmons et al
-
Tendon Disorders in Rheumatoid Arthritis
-
Classification of Klauser et al for Wrist Tenosynovitis in Rheumatoid Arthritis Using Ultrasonography
-
Scoring Fatty Lesions and Erosions Involving the Sacroiliac Joints (SIJ) on MRI in a Patient with Axial Spondyloarthritis
-
Screening Criteria from the Dublin Uveitis Evaluation Tool (DUET) for Spondyloarthritis and Inflammatory Backache
-
Risk Factors of Maurer et al for Worsening of Skin Fibrosis in a Patient with Diffuse Cutaneous Systemic Sclerosis (dcSSc)
-
Immunodeficiency Associated with Thymoma (Good's Syndrome)
-
WHIM Syndrome (Warts, Hypogammaglobulinemia, Infection, Myelokathexis)
-
Osteolytic Bone Lesions in Osseous Sarcoidosis Mimicking Metastatic Carcinoma
-
MRI Tenosynovitis Score of Lambot et al in a Patient with Juvenile Idiopathic Arthritis
-
Risk Factors of Guillaume et al for Complications in a Patient Presenting with Oligoarticular Juvenile Rheumatoid Arthritis (JRA)
-
Classification of Dale et al for Radiographic Changes in the Knee for a Patient with Juvenile Rheumatoid Arthritis (JRA)
-
Eurofever Clinical Criteria for TRAPS (TNF-Receptor Associated Periodic Syndrome)
-
Eurofever Clinical Criteria for CAPS (Cryopyrin-Associated Periodic Syndrome)
-
Eurofever Clinical Criteria for MKD (Mevalonate Kinase Deficiency, Hyper-IgD Syndrome)
-
Eurofever Clinical Criteria for FMF (Familial Mediterranean Fever)
-
Criteria of Yalcinkaya et al for the Diagnosis of Familial Mediterranean Fever in a Child
-
Predictors of Legge et al for Progression of Organ Damage in a Patient with Systemic Lupus Erythematosus (SLE)
-
Familial Chilblain Lupus (FCL)
-
Elderly Onset Rheumatoid Arthritis (EORA, Late Onset RA) versus Younger-Onset Rheumatoid Arthritis (YORA)
-
Risk Factors of Salmon et al for Serious Infection in a Patient with Rheumatoid Arthritis Treated with Abatacept (Orencia)
-
Criteria of Grossman et al for Diagnosis of Giant Cell Arteritis (Temporal Arteritis) When the Temporal Artery Biopsy (TAB) Is Negative
-
Classification of Kone-Paut et al for Pediatric Behcet’s Disease
-
Sclerotic-Type (Scleroderma-Like) Chronic Graft versus Host Disease (GVHD) Following Allogeneic Hematopoietic Stem Cell Transplant (HSCT)
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Skin Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Mouth and Gastrointestinal Tract Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Lung Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Ocular (Eye) Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Female Genital Tract Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Liver (Hepatic) Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Joint and Fascia Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Other Site Involvement
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Performance Score and Summary Status
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Categories of Acute and Chronic GVHD
-
National Institutes of Health Criteria for Clinical Trials in Chronic Graft-versus-Host Disease (GVHD): Global Score
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Constitutional Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Lymphadenopathy Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Glandular Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Articular Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Cutaneous Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Pulmonary Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Renal Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Muscle Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Peripheral Nervous System (PNS) Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Central Nervous System (CNS) Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Hematological Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Biological Subscore
-
EULAR Primary Sjogren’s Syndrome Disease Activity (ESSDAI): Total Score
-
EULAR Sjogren's Syndrome Patient Reported Index (ESSPRI)
-
Simplified Version of the Ankylosing Spondylitis Disease Activity Score (SASDAS)
-
Reactive Arthritis in a Patient with Giardiasis
-
American College of Rheumatology (ACR) Composite Response Index for Systemic Sclerosis (CRISS): Failure to Improve
-
American College of Rheumatology (ACR) Composite Response Index for Systemic Sclerosis (CRISS): Probability of Improvement
-
Red Flags of Li et al for a Patient with Scleroderma
-
Predictive Factors of Xu et al for Rapidly-Progressive Interstitial Lung Disease (ILD) in a Patient with Clinically Amyopathic Dermatomyositis (CADM)
-
Ocular Myasthenia Gravis (OMG)
-
Pediatric Myasthenia Gravis
-
Preliminary Criteria of De Vita et al for the Diagnosis of Cryoglobulinemic Vasculitis
-
Criteria of Ravelli et al for Macrophage Activation Syndrome (MAS) Complicating Systemic Juvenile Idiopathic Arthritis (JIA)
-
Risk Factors of Guzman et al for Flares in a Patient with Juvenile Idiopathic Arthritis (JIA)
-
Chronic Arthritis Score (CASco) of Cattalini et al for Evaluating a Child with Musculoskeletal Complaints
-
International Severity Scoring System of Demirkaya et al for Familial Mediterranean Fever (FMF, ISSF)
-
Diagnostic Criteria of Jansson et al for Nonbacterial Osteitis (NBO)
-
Lupus Low Disease Activity State (LLDAS) of Franklyn et al for a Patient with SLE
-
Classification Criteria of the American College of Rheumatology (ACR) and the European League Against Rheumatism (EULAR) for Primary Sjogren's Syndrome (SS)
-
Prognostic Factors of Brito-Zeron et al for a Patient with Primary Sjogren's Syndrome
-
Revised Criteria of Valentini et al for Activity of Systemic Sclerosis (Revised EUSTAR Activity Index)
-
Dermatomyositis Skin Severity Index (DSSI) of Carroll et al
-
STING-Associated Vasculopathy with Onset in Infancy (SAVI)
-
Skin Lesions in Patients with IgG4-Related Disease
-
Allergy to Alpha-Gal (Red Meat Allergy Syndrome)
-
Time Course of an Immune Response to an Antigenic Stimulus (Primary and Secondary Immune Response)
-
SLEDAI-2K Score for Systemic Lupus Erythematosus (SLE)
-
Lupus Headache
-
Lupus Tumidus (Lupus Erythematosus Tumidus)
-
Extra-Articular Involvement and Complications of Rheumatoid Arthritis
-
Leeds Enthesitis Index (LEI) of Healy and Helliwell
-
Enthesitis Index of the Spondyloarthritis Research Consortium of Canada (SPARCC)
-
ASAS Classification Criteria for Peripheral Spondyloarthritis
-
Capillaroscopic Skin Ulcer Risk Index (CSURI) for a Patient with Systemic Sclerosis
-
Significance of Skin Telangiectasia for a Patient with Systemic Sclerosis Based on the Study of Hurabielle et al
-
Clinical Findings of McCann and Pain Associated with Severe Juvenile Dermatomyositis (JDM)
-
Clinical Predictors of Wang et al for Prognosis in a Patient with Myasthenia Gravis
-
Drug-Induced Exacerbation of Myasthenia Gravis (MG)
-
Refractory Myasthenia Gravis (MG)
-
Diagnostic Criteria of Sudulagunta et al for Myasthenia Gravis (MG)
-
Clinical Features of Myasthenia Gravis Associated with Anti-MuSK (IgG4-Related MG)
-
Transient Neonatal Myasthenia Gravis (TNMG)
-
Eosinophilic Arthritis
-
Idiopathic CD4 Lymphocytopenia (ICL, Pseudo-HIV Disease)
-
Age-Related Immunodeficiency (Senile Immunodeficiency, Immune Senescence)
-
Immunocompromising Conditions of Tande et al
-
Autoimmune Paraneoplastic Syndromes in Patients with the Myelodysplastic Syndrome (MDS)
-
Criteria of Vodovar et al for Drug Fever (DF)
-
Cardiovascular Manifestations in IgG4-Related Disease
-
Prognostic Factors of Shi et al for a Patient with Antisynthetase Autoantibodies
-
Autoinflammatory Disease Damage Index (ADDI) of ter Haar et al
-
Lupus Mesenteric Vasculitis
-
Differential Diagnosis of an Elevated Serum Creatine Kinase (CK) in a Patient with Systemic Lupus Erythematosus (SLE)
-
Pseudo-SLE Associated with Parvovirus B19 Infection
-
Diffuse Alveolar Hemorrhage (DAH) in a Patient with Systemic Lupus Erythematosus (SLE)
-
Intestinal Pseudo-Obstruction (IPO) in Systemic Lupus Erythematosus (SLE)
-
Predictors of Lim et al for the Damage Trajectory of a Patient with Juvenile-Onset Systemic Lupus Erythematosus (SLE)
-
Hyperviscosity Syndrome in Rheumatoid Arthritis (RA)
-
Criteria of de Hair et al for Difficult-to-Treat Rheumatoid Arthritis (RA)
-
Clinical and Laboratory Findings Associated with a Worse Prognosis for a Patient with Rheumatoid Arthritis (RA)
-
EULAR/PReS Criteria for Childhood Vasculitides: Childhood Polyarteritis Nodosa (PAN)
-
EULAR/PReS Criteria for Childhood Vasculitides: Description of Childhood Cutaneous Polyarteritis
-
Markers of Kato et al for Relapse of Cutaneous Polyarteritis Nodosa
-
EULAR/PReS Criteria for Childhood Vasculitides: Wegener's Granulomatosis (Granulomatosis with Polyangiitis)
-
Risk Factors of Charlier et al for Major Infections in a Patient with Wegener's Granulomatosis
-
Aortitis in a Patient with Giant Cell Arteritis (GCA)
-
EULAR/PReS Criteria for Childhood Vasculitides: Henoch Schonlein Purpura
-
2008 Criteria of EULAR/PRINTO/PRES for Pediatric Henoch-Schonlein Purpura
-
Indications for Admitting a Patient with Henoch-Schonlein Purpura (HSP) Into the Hospital
-
EULAR/PReS Criteria for Childhood Vasculitides: Takayasu Arteritis
-
Risk of Malignancy in a Patient with Intestinal Behcet's Disease
-
EULAR/PReS Criteria for Childhood Vasculitides: Classification
-
Combined Arteritis Damage Score (CARDS) of Nakagomi et al for Large Vessel Vasculitis
-
Criteria of Poddubnyy et al for Referral of a Patient with Suspected Axial Spondyloarthritis to a Rheumatologist (ASAS Recommendations)
-
Scleroderma Acrosclerosis
-
Classification of Peterson et al for Morphea (Localized Scleroderma, Mayo Clinic Classification)
-
Skin Thickness Progression Rate (STPR) of Domsic et al for a Patient with Diffuse Scleroderma
-
Prediction Rule of Domsic et al for Two Year Mortality for a Patient with Early Diffuse Cutaneous Systemic Sclerosis
-
2013 ACR/EULAR Classification Criteria for Systemic Sclerosis
-
Systemic Sclerosis and Systemic Lupus Erythematosus (SLE) Overlap Syndrome (Lupoderma)
-
Juvenile Idiopathic Inflammatory Myopathy with Anti-HMGCR Autoantibodies
-
Predictors of Mazzoli et al for Progression from Ocular to Generalized Myasthenia Gravis
-
Fetal Acetylcholine Receptor (ACR) Inactivation Syndrome
-
Myasthenia Gravis Status and Treatment Intensity (MGSTI)
-
PURE-4 Scale of Audureau et al Psoriatic Arthritis Screening
-
EULAR Criteria for Arthralgia at Risk for Rheumatoid Arthritis
-
Clinical Prediction Rule of van de Stadt et al for Predicting Arthritis in a Seropositive Patient with Arthralgia
-
Arthralgia or Arthritis Associated with Parasitic Disease
-
HUPI Index of Castrejon et al for Evaluating a Patient with Early Arthritis
-
ICF Syndrome (Immunodeficiency, Centromeric Instability, Facial Anomalies)
-
Granulomatous Common Variable Immune Deficiency (CVID) Mimicking Sarcoidosis
-
Differentiating Common Variable Immunodeficiency (CVID) from IgG Deficiency
-
Allergic Contact Cheilitis
-
Predictors of Vorselaars et al for Relapse of Sarcoidosis Following Discontinuation of Infliximab Therapy
-
10 Joint Juvenile Arthritis Disease Activity Score (JADAS-10) of Consolaro et al
-
Disease Activity States of Consolaro et al for Nonsystemic Juvenile Idiopathic Arthritis Based on the 3-Item cJADAS10
-
NLRP1-Associated Autoinflammation with Arthritis and Dyskeratosis (NAIAD)
-
Chronic Atypical Neutrophilic Dermatosis with Lipodystrophy and Elevated Temperature (CANDLE) Syndrome
-
Paraneoplastic Large Vessel Vasculitis with Aortitis
-
Clinical Score of Jansson et al for Nonbacterial Osteitis (NBO)
-
Criteria of Masaki et al for IgG4-Related Mikulicz's Disease
-
Criteria of Kawano et al for IgG4-Related Kidney Disease
-
Comprehensive Criteria for the Diagnosis (CCD) of Umehara et al for IgG4-Related Disease
-
Organ Involvement in IgG4-Related Disease
-
Differential Diagnosis of an Elevated Serum IgG4 Concentration
-
Clinical Features of the Aicardi-Goutieres Syndrome
-
Clinical and Pathologic Features of Eosinophilic Fasciitis (EF, Shulman Disease)
-
Systemic Immune-Inflammation Index (SIII)
-
Platelet-to-Lymphocyte Ratio (PLR)
-
Neutrophil-to-Lymphocyte Ratio (NLR)
-
EULAR Criteria for Arthralgia That Is Suspicious for Progression to Rheumatoid Arthritis (RA)
-
Double and Triple Seronegative Rheumatoid Arthritis
-
Prognostic Factors of Fan et al for a Pediatric Patient with Takayasu's Arteritis
-
Risk Factors of Gordon et al for Scleroderma Renal Crisis That Can Be Identified at the Time of Scleroderma Diagnosis
-
Diagnostic Criteria for Nakajo-Nishimura Syndrome (NNS)
-
Joint Contractures, Muscular Atrophy, Microcytic Anemia and Panniculitis-Associated Lipodystrophy (JMP Syndrome)
-
Japanese Autoinflammatory Syndrome with Lipodystrophy (JASL)
-
Lupus Mimics/Mimickers
-
2019 EULAR/ACR Classification Criteria for Systemic Lupus Erythematosus
-
Rheumatoid Arthritis Refractory to Therapy
-
Clinical Arthritis Rule (CARE) of ten Brinck for Recognition of Early Inflammatory Arthritis
-
Japanese Vasculitis Activity Score (JVAS) for MPO-ANCA Positive Microscopic Polyangiitis with Renal Involvement
-
Risk Factors of Yamaguchi for Severe Infection in a Patient with ANCA-Associated Vasculitis Receiving Immunosuppressive Therapy
-
Grading System of Lee et al for the Cytokine Release Syndrome (CRS)
-
Predictive Factors of Yang et al for Macrophage Activation Syndrome (MAS) in a Patient with Adult-Onset Still's Disease (AOSD)
-
Risk Factors for Candida Pericarditis
-
Systemic Lupus Erythematosus Disease Activity Score (SLE-DAS) of Jesus et al
-
Criteria of Brunner et al for a Flare in Childhood-Onset Systemic Lupus Erythematosus (SLE): SLEDAI-Based Flare Score
-
Criteria of Brunner et al for a Flare in Childhood-Onset Systemic Lupus Erythematosus (SLE): BILAG-Based Flare Score
-
Model of Elman et al for the Diagnosis of Discoid Lupus Erythematosus (DLE)
-
Criteria of Aletaha et al for Disease Activity in Rheumatoid Arthritis
-
Risk Factors of Hocevar et al for a Severe Cranial Ischemic Event Associated with Giant Cell Arteritis
-
Risk Factors of Salvarani et al for Cranial Ischemic Events (CIE) Associated with Giant Cell Arteritis
-
Clinical Findings of van der Geest in the Diagnosis of Giant Cell Arteritis (GCA)
-
Indian Takayasu's Arteritis Activity Score (ITAS2010 and ITAS.A)
-
Score of Davatachi et al for the Diagnosis of Behcet's Disease
-
Endothelial Activation and Stress Index (EASIX) of Luft et al in Acute Graft-versus-Host Disease (GVHD)
-
Relapsing Polychondritis Damage Index (RPDAM) of Mertz et al
-
Relapsing Polychondritis Disease Activity Index (RPDAI) of Arnaud et al
-
ASAS Classification Criteria for Axial Spondyloarthritis: Sets 1 and 2
-
Glasgow Ultrasound Enthesitis Scoring System (GUESS) for the Lower Extremities
-
Scleroderma Clinical Trials Consortium Damage Index (SCTC-DI)
-
Linear Scleroderma (Morphea) with Facial En Coup Sabre (ECS)
-
Angioedema Associated with Angiotensin Converting Enzyme Inhibition (ACEI)
-
Scurvy Mimicking a Rheumatic Disorder
-
Differential Diagnosis of Acute Monoarthritis
-
Indications to Refer a Patient with Acute Monoarthritis
-
Criteria of Davila et al for Severe Cytokine Release Syndrome (CRS)
-
Rituximab-Associated Flare of Mixed Cryoglobulinemia Vasculitis
-
IgG4-Related Disease (IgG4-RD) Responder Index of Carruthers et al
-
Celiac Disease Co-Existing with Systemic Lupus Erythematosus
-
Predictors of Cho et al for a Flare in a Stable Asian Patient with Systemic Lupus Erythematosus (SLE)
-
Criteria of Polachek et al for Low Disease Activity (LDA) in a Patient with Systemic Lupus Erythematosus (SLE)
-
Criteria of Zen et al for Minimal Disease Activity (MDA) in a Patient with Systemic Lupus Erythematosus (SLE)
-
Responder Index of Furie et al for a Patient with Systemic Lupus Erythematosus (SLE)
-
Lupus Hepatitis
-
Refractory Ascites in a Patient with Systemic Lupus Erythematosus (SLE)
-
Risk Factors of Huang et al for Seizures in a Patient with Systemic Lupus Erythematosus (SLE)
-
Oral Mucosal Lupus Erythematosus
-
Definition of Remission in Systemic Lupus Erythematosus (DORIS)
-
Lupus Myelitis
-
Systemic Lupus Erythematosus (SLE) Associated Acute Pancreatitis
-
Lupus Esophagus
-
Systemic Lupus Erythematosus (SLE) Associated Sjogren's Syndrome
-
EULAR Definition of Difficult-to-Treat Rheumatoid Arthritis
-
Matrix of Vanier et al for Prediction of Rapid Radiographic Progression of Early Rheumatoid Arthritis (RA)
-
Manifestations of Henoch-Schonlein Purpura in the Central Nervous System
-
Angiographic Classification of Numano et al for Takayasu Arteritis
-
Classification of Goel et al for Angiographic Distribution of Takayasu Arteritis
-
Distal Renal Tubular Acidosis Associated with Sjogren's Syndrome
-
ANCA-Associated Vasculitis with Bronchiectasis
-
Vasculitis Associated with Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia (CMML)
-
Risk Factors of Michelena et al for Renal Impairment in Axial Spondyloarthritis
-
Gastrointestinal Involvement in Systemic Sclerosis (Scleroderma)
-
Risk Factors of Mihai et al for Gangrene in a Patient with Systemic Sclerosis
-
Systemic Sclerosis-Related Myocarditis
-
Hand Morbidities Associated with Systemic Sclerosis
-
Spanish Scleroderma Risk Score (RESCLESCORE) of Rubio-Rivas et al
-
Predictors of Panopoulos et al for Mortality in a Patient with Systemic Sclerosis
-
Prediction Rule of van den Hombergh et al for Diffuse Cutaneous Systemic Sclerosis
-
Predictors of Scussel-Lonzetti et al for Mortality Due to Systemic Sclerosis
-
Prediction Rule of Domsic et al for 5-Year Mortality Rate for a Patient with Early Diffuse Cutaneous Systemic Sclerosis
-
Model of Beretta et al for 5-Year Mortality for a Patient with Systemic Sclerosis
-
Polymyositis with Mitochondrial Pathology (PM-Mito)
-
Poor Prognostic Factors (PPF) in Psoriatic Arthritis and Response to Abatacept Therapy
-
Loss of Immune Memory (Immune Amnesia) Following an Acute Measles Infection
-
Congenital Sideroblastic Anemia, B-Cell Immunodeficiency, Periodic Fevers and Developmental Delay (SIFD) Associated with Mutations in TRNT1
-
Opioid-Related Immunosuppression
-
T-Cell Exhaustion
-
LRBA Deficiency
-
Delayed Pressure Urticaria (DPU)
-
Therapy of Cold Agglutinin Disease with Sutimlimab
-
University of Pennsylvania (Penn) Cytokine Release Syndrome (CRS) Grading System
-
Muscular Sarcoidosis
-
Algorithm of Bilgin et al for Distinguishing Adult-Onset Still's Disease (AOSD) from Other Causes of Fever of Unknown Origin (FUO)
-
MS Score of Minoia et al for Macrophage Activiation Syndrome (MAS) in Systemic Juvenile Idiopathic Arthritis (sJIA)
-
Systemic Manifestation Score (SMS) of Saccomanno et al for a Patient with Systemic Juvenile Idiopathic Arthritis (sJIA)
-
Predictors of Saccomanno et al for Response to Anakinra by a Patient with Systemic Juvenile Idiopathic Arthritis (sJIA)
-
Clinical Features of the VEXAS Autoinflammatory Syndrome Associated with Somatic Mutations in UBA1
-
Modified Score of Pras et al for Severity of Familial Mediterranean Fever (FMF) in Children
-
Score of Pras et al for Severity of Familial Mediterranean Fever (FMF)
-
SS2 Score of Mor et al for the Clinical Severity of Familial Mediterranean Fever (FMF)
-
Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Familial Mediterranean Fever (FMF)
-
Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Mevalonate Kinase Deficiency (MKD)
-
Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Tumor Necrosis Factor-1 Associated Periodic Syndrome (TRAPS)
-
Auto-Inflammatory Diseases Activity Index (AIDAI) Diary: Daily Record for a Patient with Cryopyrin-Associated Periodic Syndrome (CAPS)
-
Misdiagnosis of Antisynthetase Syndrome (Anti-Jo-1 Syndrome) as Rheumatoid Arthritis
-
Diagnostic Criteria of Pinal-Fernandez et al al for Eosinophilic Fasciitis (EF, Shulman Disease)
-
Lymphocyte-to-Monocyte Ratio
-
Neutrophil-to-Platelet Ratio (NPR)
-
Systemic Inflammation/Inflammatory Response Index (SIRI)
-
The World Allergy Organization Subcutaneous Immunotherapy Systemic Reaction Grading System
-
Subclinical Rejection (SCR, Subclinical Acute Rejection)
-
Elevated Serum Lactate in a Patient with Chronic Fatigue Syndrome
-
Pediatric Systemic Lupus Erythematosus (SLE) Associated with Constitutional Mismatch Repair Deficiency (CMMRD)
-
Criteria of Lambers et al for Incomplete Systemic Lupus Erythematosus (SLE)
-
Risk Factors of Curtis et al for Gastrointestinal Perforation in a Patient with Rheumatoid Arthritis
-
Predictors of Syngle et al for Autonomic Neuropathy in a Patient with Rheumatoid Arthritis
-
Systemic Sclerosis-Mixed Connective Tissue Disease (SSc-MCTD)
-
Systemic Sclerosis Overlap Syndromes
-
Drug-Induced Arthritis and Arthralgia
-
Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Manifestation Grades
-
Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Additional Findings
-
Immune Deficiency and Dysregulation Activity (IDDA) Score of Tesch et al: Final Score Determination
-
Clinical Findings That May Be Clues to a Primary Immunodeficiency
-
ESID/PAGID 1999 Criteria for Common Variable Immunodeficiency Disorder (CVID)
-
ESID 2014 Criteria for Common Variable Immunodeficiency Disorder (CVID)
-
Differential Diagnosis of a Patient with Hypopigmentation and Primary Immunodeficiency
-
Vici Syndrome (VICIS)
-
Diagnostic Criteria of Ameratunga et al for Common Variable Immune Deficiency (CVID)
-
Interleukin 1 Receptor Associated Kinase 4 (IRAK-4) Deficiency
-
X-Linked Agammaglobulinemia (XLA)
-
Griscelli Syndrome
-
Immunodeficiency Associated with an IgG Subclass Deficiency
-
MYD88 Deficiency
-
Immunodeficiency Associated with LAMTOR2 (p14) Deficiency
-
IKBKG and NFKBIA Deficiencies
-
Photoallergic Contact Dermatitis (PACD) Score of Cazzaniga et al
-
Criteria of Kahn and Appleboom for Mixed Connective Tissue Disease (MCTD)
-
Clinical and Laboratory Findings of John et al for Mixed Connective Tissue Disease (MCTD)
-
Refractory Familial Mediterranean Fever (FMF)
-
Prognostic Factors of Tang et al for Microscopic Polyangiitis (mPA) with Diffuse Alveolar Hemorrhage (DAH)
-
Hiker's Feet in Anti-Synthetase Syndrome
-
Criteria of Shoenfeld and Agmon-Levin for Autoimmune/Inflammatory Syndrome Induced Adjuvants (ASIA)
-
Neurologic Severity Scale of Adang et al for Aicardi Goutieres Syndrome (AGS Scale)
-
SLEDAI 2K glucocorticoid index
-
Infections That Mimic Rheumatoid Arthritis
-
General Synovitis Score (GSS) and Immunologic Synovitis Score (ISS) for Evaluating a Patient with Rheumatoid Arthritis (RA)
-
2022 ACR/EULAR Classification Criteria for Eosinophilic Granulomatosis with Polyangiitis (EGPA)
-
2022 ACR/EULAR Classification Criteria for Granulomatosis with Polyangiitis (GPA)
-
Polymyalgia Rheumatica Activity Score (PMR-AS)
-
Score of Nagamori et al for Predicting Severe Gastrointestinal Disease Due to Henoch-Schonlein Purpura
-
Prognostic Factors of Sugiyama et al for Interstitial Lung Disease (ILD) in a Patient with Polymyositis or Dermatomyositis
-
Autoimmune Findings as a Warning Sign of Primary Immunodeficiency in a Pediatric Patient
-
Pulmonary Complications Associated with Primary Immunodeficiency Syndromes
-
Neonatal Lymphopenia and Severe Combined Immunodeficiency (SCID)
-
PSTPIP1-Associated Myeloid-Related Proteinemia Inflammatory (PAMI) Syndrome
-
2022 ACR/EULAR Classification Criteria for Microscopic Polyangiitis (MPA)
-
Advanced Lung Cancer Inflammation Index (ALI)
-
Gustave Roussy Immune Score (GRIm-Score) of Bigot et al
-
Predictors of Carvalho et al for Infection in a Hospitalized Patient with Systemic Lupus Erythematosus (SLE)
-
Evaluation of a Patient with Systemic Lupus Erythematosus (SLE) with Hospitalization as the Presenting Event
-
Bullous Systemic Lupus Erythematosus (SLE)
-
SLE Risk Probability Index (SLERPI)
-
Predictors of Floris et al for a Flare in Systemic Lupus Erythematosus (SLE)
-
Geode in Rheumatoid Arthritis
-
Criteria of Yamamoto and Oiwa for the Diagnosis of Polyarteritis Nodosa (PAN)
-
Giant Cell Arteritis (GCA) Halo Score
-
Prediction Model of Ing et al for Suspected Giant Cell Arteritis (GCA)
-
Model of Weis et al for Identifying a Patient Whose Temporal Artery Biopsy is LIkely to Be Positive for Giant Cell Arteritis (GCA)
-
Differential Diagnosis of Cutaneous Leukocytoclastic Vasculitis
-
Neonatal Behcet's Disease
-
Nomogram of Gendreau et al for Poor Outcome in a Patient with Systemic Vasculitis Involving the Gastrointestinal Tract
-
Cutaneous Manifestations of ANCA-Associated Vasculitis
-
Conditions Associated with HLA-B27
-
Markers of Dumitru et al for Subclinical Heart Involvement in a Patient with Systemic Sclerosis
-
Risk Factors of Mihai et al for Gangrene in a Patient with Systemic Sclerosis
-
Risk Factors of Dein et al for Pseudo-Obstruction in Systemic Sclerosis
-
Prognostic Factors of Sag et al for a Patient with Juvenile Dermatomyositis
-
PRINTO Criteria for Clinically Inactive Juvenile Dermatomyositis
-
Manual Muscle Testing on a Subset of Eight Muscles (MMT8) in Idiopathic Inflammatory Myopathies
-
Muscle Biopsy Scoring System of Wedderburn et al for Juvenile Dermatomyositis: Inflammatory and Vascular Domains
-
Muscle Biopsy Scoring System of Wedderburn et al for Juvenile Dermatomyositis: Muscle Fiber, Connective Tissue and Global Domains
-
Skin Conditions Associated with Primary Immunodeficiencies: Eczema
-
Skin Conditions Associated with Primary Immunodeficiencies: Abscess
-
Skin Conditions Associated with Primary Immunodeficiencies: Disseminated Warts (HPV-Positive Skin Lesions)
-
Skin Conditions Associated with Primary Immunodeficiencies: Granuloma Formation
-
Skin Conditions Associated with Primary Immunodeficiencies: Mucocutaneous Candidiasis
-
Skin Conditions Associated with Primary Immunodeficiencies: Nail Changes
-
Skin Conditions Associated with Primary Immunodeficiencies: Hair Anomaly
-
Skin Conditions Associated with Primary Immunodeficiencies: Psoriasis-Like
-
Skin Conditions Associated with Primary Immunodeficiencies: SLE-like Skin Lesions
-
Skin Conditions Associated with Primary Immunodeficiencies: Alopecia
-
Skin Conditions Associated with Primary Immunodeficiencies: Mycobacterial Infection
-
Mucocutaneous Conditions Associated with Primary Immunodeficiencies: Oral Changes
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Skin Conditions Associated with Primary Immunodeficiencies: Skin Ulcers
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Skin Conditions Associated with Primary Immunodeficiencies: Molluscum Contagiosum
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Skin Conditions Associated with Primary Immunodeficiencies: Skin Pigmentation
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Skin Conditions Associated with Primary Immunodeficiencies: Skin Rash
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Skin Conditions Associated with Primary Immunodeficiencies: Petechiae
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Skin Conditions Associated with Primary Immunodeficiencies: Miscellaneous Skin Changes
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Infections in the Differential Diagnosis of Adult Still's Disease
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Paraneoplastic Adult Still's Disease
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Refractory Systemic Onset Juvenile Idiopathic Arthritis (SJIA)
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FMF50 for Assessing Responsiveness of Therapy in Familial Mediterranean Fever (FMF)
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2019 ACR and EULAR Criteria for IgG4-Related Disease: Exclusion Criteria
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2019 ACR and EULAR Criteria for IgG4-Related Disease: Inclusion Criteria
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2019 ACR and EULAR Criteria for IgG4-Related Disease: Criteria for Diagnosis
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Model of Hoi et al for Calculating the Probability of High Disease Activity (HDA) in Systemic Lupus Erythematosus (SLE)
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2022 ACR/EULAR Classification Criteria for Giant Cell Arteritis (GCA)
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Post-Streptococcal Henoch Schonlein Purpura
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Clinical Features of Childhood Sjogren Syndrome
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Pseudo-Ankylosing Spondylitis Associated with Ochronosis
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Criteria of Oldroyd et al for Cancer Screening in a Patient with Idiopathic Inflammatory Myopathy
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Seronegative Polyarthritis Without Myositis Associated with Anti-NXP2 Antibodies
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Cancer Screening Protocol of Oldroyd et al in a Patient with Idiopathic Inflammatory Myopathy
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Differential Diagnosis of an Arthropathy Affecting the Spine and Peripheral Joints
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Criteria for Primary Natural Killer Cell Deficiency (NKD)
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Classification for Primary Natural Killer Cell Deficiency (NKD)
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Diagnostic Algorithm Natural Killer Cell Deficiency (NKCD)
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Anti-PL12 Syndrome (Anti-Aminoacyl-tRNA Synthetase Syndrome, ARS)
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Derived Neutrophil to Lymphocyte Ratio (dNLR)
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Systemic Inflammation Score (SIS) of Chang et al
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Memorial Sloan Kettering Prognostic Score (MPS)
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Pan-Immune-Inflammation Value (PIV)
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Predictors of Assuncao et al for Hospitalization of a Patient with Systemic Lupus Erythematosus (SLE)
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Model of Vanier et al for Predicting Rapid Radiographic Progression of Early Rheumatoid Arthritis
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Predictors of Khader et al for Remission of Rheumatoid Arthritis with Biologic Therapy
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Algorithm of Lecler et al for Diagnosis of Giant Cell Arteritis (GCA) by Imaging Studies
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Algorithm of Lecler et al for Diagnosis of Giant Cell Arteritis (GCA) by Imaging Studies: MRI Scoring
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Score of El-Dairi e al for Giant Cell Arteritis
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Conditions in the Differential Diagnosis of Giant Cell Arteritis
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Diagnostic Models of Czihal et al for Giant Cell Arteritis
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Clinical Criteria for Giant Cell Arteritis Based on the GiACTA Trial
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Score of Laskou et al for Diagnosis of Giant Cell Arteritis (GCA, Southend Score)
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Prognostic Model of Levine et al for Acute Graft-versus-Host Disease Using Serum Biomarkers (Ann Arbor Score)
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Day 100 Score of Metafuni et al for Prediction Moderate to Severe cGVHD After a Hematopoietic Cell Transplant
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High-Risk Indicators of Fan et al for Central Nervous System (CNS) Involvement in Primary Sjogren's Syndrome
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Clinical Findings of Fan et al for Central Nervous System (CNS) Involvement in Primary Sjogren's Syndrome
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Nomogram of Ye et al for Predicting Axial Spondyloarthritis
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Systemic Sclerosis Sine Scleroderma (ssSSc)
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ONCOREUM Score of Civino et al for Distinguishing Childhood Cancer with Arthropathy from Juvenile Idiopathic Arthritis (JIA)
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Model of Xu et al for Predicting Bloodstream Infection (BSI) in a Patient with Fever of Unknown Origin (FUO)
