20 results
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
 •
Introduction & Pathophysiology ... Epidemiology • Clinical ... AorticValve #cardiology #peds
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
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
How to use C-reactive protein (CRP)- Review https://ep.bmj.com/content/early/2018/07/19/archdischild-2018-315079

 - An CRP alone cannot be used to
biomarker the clinical ... correlate with the likelhood ... VisualAbstract #Review #Peds
Whistling Cough- A 4-year-old boy presented to the otorhinolaryngology outpatient clinic with a 2-day history of
otorhinolaryngology outpatient clinic ... performed, given the likelihood ... #NEJM #clinical ... #chest #xray #peds
Heparin Induced Thrombocytopenia (HIT) - Diagnosis and Management - GrepMed Handbook

Presentation: 
 • Plts ↓50% (nadir
♀, ↑Age, ESRD Pathophysiology ... Diagnosis: • Clinical ... non-heparin A/C if clinical ... thrombosis or high likelihood
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
While the pathophysiology ... Sign #Meningitis #Clinical ... PhysicalExam #Pediatrics #Peds
â–º
Acute Otitis Media: Pathogenesis and Clinical Findings (in Children)
Upper Respiratory Tract Infection: 
 - Bacterial: Streptococcus
Pathogenesis and Clinical ... #OtitisMedia #pathophysiology ... symptoms #signs #peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds