173 results
diagnosis differential causes cardiology clinical algorithm management pathophysiology pharmacology cardiomyopathy peds pediatrics table endocrinology treatment hematology syndrome nejm signs echocardiogram
Harlequin Ichthyosis Rare genetic disorder that results in thickened skin over nearly the entire surface of the
Ichthyosis Rare genetic ... physicalexam #pediatrics #genetics
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 First10EM Post Intubation Checklist #Management #Airway #CriticalCare #PostIntubation #Checklist #First10EM
First10EM Post Intubation ... PostIntubation #Checklist #First10EM
The following table from MacGregor (1997) summarizes the bioavailability of many commonly used antibiotics: #EBM #Pharmacology #InfectiousDiseases
Antibiotics #Absorption #Kinetics ... Bioavailability #Table #first10em
Metabolism of plasma lipoproteins and related genetic diseases - Familial Hypercholesterolemia Type I (FAMILIAL HYPERCHYLOMICRONEMIA) Type IIA
lipoproteins and related genetic ... #lipoproteins #genetics
Role of G6PD in Protection against Oxidative Damage #Pathophys #Peds #Genetics #Honc #Favism #g6pd #NEJM
Pathophys #Peds #Genetics
Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
#Table #NICU #Genetics
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
MetabolicEmergency #Genetics
Autosomal Dominant Inheritance - Most common mode of Mendelian inheritance - Affected individual carries the
#Inheritance #Genetics
Causes of Hypomagnesemia - Differential Diagnosis Algorithm GI LOSS - FeMg < 2-2.5% or 24h Urine Mg
other EGFR ab • Genetics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics
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