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hematology management rheumatology signs anemia aplastic behcet cryofibrinogenemia dermatology disease hand henochscholeinpurpura hsp iga lcv leukocytoclastic oncology pathophysiology skinrash vancomycin
IgA Vasculitis – Henoch Scholein Purpura: Pathogenesis and Clinical Findings - Infectious Agents - 50% have
Pathogenesis and Clinical ... , vomiting, GI bleeding ... nephrotic/nephritic syndrome ... Pathophysiology #Diagnosis ... #Signs #Symptoms
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
association • M > F Clinical ... meningitis), MCC CNS symptoms ... (Clinical Dx). ... oral ulcers in 12 ... #signs #symptoms
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... ecchymoses, mucosal bleeding ... - Parvovirus B19 ... • Improve the symptoms ... oncology #hematology #diagnosis
Vancomycin induced Leukocytoclastic Vasculitis (LCV) of the Hand 70 M vertebral osteomyelitis on vancomycin and cefepime for
Diagnosis? ... eosinophilia and systemic symptoms ... Churg-Strauss syndrome ... #dermatology #clinical ... #photo
Cryofibrinogenemia Summary Cryofibrinogenemia Epidemiology: • 40-70 years with a modest female predominance Cryofibrinogenemia: • The precipitation of a
Cryofibrinogenemia Symptoms ... Paradoxical spontaneous bleeding ... malignancies, vasculitis ... : • + Clinical ... Antiphospholipid syndrome
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