24 results
diagnosis differential algorithm clinical pathophysiology pediatrics peds pharmacology signs anxiety cardiology comparison diseases ebm endocrinology hypomagnesemia iem inbornerrors low magnesium
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
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
Causes of Hypomagnesemia - Differential Diagnosis Algorithm GI LOSS - FeMg < 2-2.5% or 24h Urine Mg
Causes of Hypomagnesemia ... other EGFR ab • Genetics ... Magnesium #Low #Causes
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
Causes of Pelvic Organ Prolapse - Differential Diagnosis Algorithm Herniation of one or more pelvic organs Risk factors:
Causes of Pelvic ... Risk factors: genetics ... Diagnosis #Algorithm #Causes
Etiologies of Hypernatremia - Differential Diagnosis GI losses / Insensible losses Sodium Overload Transcellular Movement of Water Central Diabetes Insipidus
- Various rare genetic ... - Various rare genetic ... Differential #Diagnosis #Table ... #Causes
FIASP - Insulin Aspart vs Novolog Have you heard about Fiasp, a new version of insulin aspart
endogenous insulin kinetics ... control and can also cause ... well due to these kinetics
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
Pathogenesis of Anxiety Disorders Anxiety Disorders: A maladaptive emotional state causing fear, worry, and excessive stress, characterized by:
less internal locus ... reporting rates) • Genetics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... pathophysiology #genetics
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