45 results
diagnosis differential pathophysiology peds causes pharmacology signs pediatrics psychiatry algorithm clinical metabolism nejm pathology symptoms endocrinology hematology honc management antibiotics
The following table from MacGregor (1997) summarizes the bioavailability of many commonly used antibiotics: #EBM #Pharmacology #InfectiousDiseases
The following table ... Antibiotics #Absorption #Kinetics ... Bioavailability #Table ... #first10em
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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 Lab patterns seen in Inborn Errors of Metabolism A table of lab values compiled from UpToDate and
Metabolism A table ... Peds #Pediatrics #Table ... #NICU #Genetics
Metabolism of plasma lipoproteins and related genetic diseases - Familial Hypercholesterolemia Type I (FAMILIAL HYPERCHYLOMICRONEMIA) Type IIA
lipoproteins and related genetic ... #lipoproteins #genetics
A schema of the pathophysiology of the inborn errors of metabolism, excluding complex storage diseases. Helps
the lab values table ... MetabolicEmergency #Genetics ... Peds #Pediatrics #Table
Role of G6PD in Protection against Oxidative Damage #Pathophys #Peds #Genetics #Honc #Favism #g6pd #NEJM
Pathophys #Peds #Genetics
Etiologies of Hypoaldosteronism Hyporeninemic Hypoaldosteronism (Low Renin, Low Aldosterone) - Diabetic Nephropathy - NSAIDs Non-Hyporeninemic Hypoaldosteronism (Normal
Critical illness - Genetic ... Sulfamethoxazole - Genetic ... Aldosterone #Comparison #Table
Causes of Hypomagnesemia - Differential Diagnosis Algorithm GI LOSS - FeMg < 2-2.5% or 24h Urine Mg
other EGFR ab • Genetics
Autosomal Dominant Inheritance - Most common mode of Mendelian inheritance - Affected individual carries the
#Inheritance #Genetics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
PraderWilli #Syndrome #genetics
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