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diagnosis pediatrics management symptoms signs neurology physicalexam video photo newborn ophthalmology radiology treatment algorithm pocus cardiology differential endocrinology msk nejm
Likelihood Ratios of Clinical Features Ruling In Deep Vein Thrombosis Malignant disease 2.71 History of deep vein thrombosis 2.25 Recent immobilization 1.98 Difference
Likelihood Ratios ... of Clinical Features ... swelling 1.45 Homans ... EBmedicine #Likelihood
Aortic Stenosis & Bicuspid Aortic Valve (AS) • Introduction & Pathophysiology • Classifications • Epidemiology •
Aortic Valve (AS ... Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
Acute Coronary Syndrome - Diagnostic Likelihood Ratios for Symptoms and Physical Examination. Source: Does This
Syndrome - Diagnostic Likelihood ... : The Rational Clinical ... Diagnosis #Cardiology #ACS
Plain radiography of the abdomen revealed calcification of both adrenal glands. A homozygous mutation in LIPA
acid lipase is critical ... #clincial #peds ... #infant #NEJM #Wolmans
Acute Coronary Syndrome - Diagnostic Likelihood Ratios for Symptoms and Physical Examination. Source: Fanaroff AC, Rymer
Syndrome - Diagnostic Likelihood ... : The Rational Clinical ... Diagnosis #Cardiology #ACS
Pediatric Pneumonia on POCUS Nothing as satisfying as when the normal lung gives way to pneumonia. -
POCUS Nothing as ... satisfying as when ... AirBronchograms #Pediatrics #Peds ... #Clinical #Lung
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 Management of patients with known or suspected malignant pleural effusion (MPE) - An Official ATS/STS/STR Clinical
- An Official ATS ... /STS/STR Clinical ... As such, the recommendation ... should be used as ... there is a low likelihood
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... lateral sclerosis Pathophysiology ... cellular function Clinical ... signs to determine likelihood ... Exam: clinical evidence
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... • Deletion of critical ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... occur in utero as ... • This is also ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds
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