16 results
diagnosis rheumatology differential treatment cardiology pharmacology signs symptoms activation anemia aplastic behcet cancer chf criticalcare decisionaid defects dermatologic disease dosing
Dermatologic Extraintestinal Manifestations in IBD - IBD Algorithm Erythema Nodosum Pyoderma Gangrenosum Metastatic Crohn's Disease Sweet Syndrome EBA Dr. Wade Billings @wabillin #Dermatologic
Dermatologic Extraintestinal ... - IBD Algorithm ... Disease Sweet Syndrome ... #Algorithm #gastroenterology ... #management #dermatology
Hypereosinophilia and Hypereosinophilic Syndrome • Secondary Hypereosinophilic Syndrome • Clinically Relevant HES Variants • When to
• Clinically ... and Treatment Algorithm ... #HES #Hematology ... eosinophils #diagnosis #management ... #algorithm
Idiopathic Inflammatory Myopathies - Dermatomyositis (DM), Immune-Mediated Necrotizing Myopathy (IMNM), Antisynthetase Syndrome (ASS), Inclusion Body Myositis
Antisynthetase Syndrome ... Body Myositis (IBM ... Idiopathic #Myopathy #Comparison ... #Managment #algorithm ... #Rheumatology #
Managing warfarin INR Warfarin dosage must be individualized according to the patient's response to the drug, and
usual INR target is ... therapeutic range) is ... #management #algorithm ... #medications #table ... decisionaid #cardiology #hematology
Our approach to the diagnosis and initial management of patients with suspected HIT. Our approach is
diagnosis and initial management ... based primarily on clinical ... #Diagnosis #Management ... #Hematology #HIT ... Thrombocytopenia #Algorithm
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... (Clinical Dx). ... Eye involvement (uveitis ... inhibitors • Uveitis ... #diagnosis #management
Inherited Qualitative Platelet Defects Bernard-Soulier Syndrome • Defect of adhesion due to a lack of GP Ib/IX/V
Bernard-Soulier Syndrome ... to a lack of GP Ib ... Platelet #Defects #comparison ... #table #differential ... #diagnosis #hematology
Macrophage Activation Syndrome (MAS) Classified among the secondary or acquired forms of haemophagocytic lymphohistiocytosis (sHLH) What? A subset of
Clinical Presentation ... failure • Fever is ... the main clinical ... #Diagnosis #Management ... #Hematology #Rheumatology
SAPHO Syndrome Summary What? SAPHO syndrome is a rare chronic inflammatory disorder of bone, joint, and skin characterized
SAPHO syndrome is ... Rheumatic pain Clinical ... Diagnosis: • A clinical ... diagnosis #management ... #Dermatology
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Constitutional Syndromes ... Aplastic Anemia Clinical ... of CD34+ cells is ... Anemia #oncology #hematology ... #diagnosis #management
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