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diabetes insulin timeline analogs antiarrhythmics cardiology classes classification peaks peds 21hydroxylasedeficiency 21ohd adrenal algorithm cah congenitaladrenalhyperplasia diagnosis dm2 genetics inpatient
Insulin Analogs - Short, Intermediate and Long Acting - Onset, Peak, Duration #Diabetes #Insulin #Analogs #Onset #Duration
- Onset, Peak, Duration ... Analogs #Onset #Duration ... #Peaks #Comparison ... #Pharmacology # ... Endocrinology #Timing
Insulin Comparison Chart - Peak and Duration Inhaled, Rapid-acting (Analog), Regular, Intermediate-Acting (NPH), Detemir, Glargine, Degludec - Stephen
Insulin Comparison ... Chart - Peak and Duration ... #Peak #Duration ... #Pharmacology # ... Endocrinology #Timing
The principles of insulin adjustment guidance - Schematic diagram of insulin onset and time action profiles
profiles - Onset and Duration ... Insulin #Analogs #Duration ... #Peaks #Comparison ... #Pharmacology # ... Endocrinology #Timing
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #pediatrics #CongenitalAdrenalHyperplasia ... #diagnosis #comparison ... treatment #Peds #Endocrinology ... #Adrenal #pathophysiology
Antiarrhythmics - Vaughan Williams Classification: CLASS 1 - Sodium Channel Blockers: • MOA: Block fast Na+ channels
effects and AP duration ... - ↑ duration ... Vaughan #Williams #Pharmacology ... Classification #Classes ... #pathophysiology
Antiarrhythmics Pharmacology Summary Cardiac Conduction Phases: Phase 0 - Ventricular Depolarization: • Na+ channels open leading to a
Antiarrhythmics Pharmacology ... - ↑ duration ... Antiarrhythmics #Pharmacology ... Classification #Classes ... #pathophysiology
Diabetes Mellitus Type 2 Inpatient Medication Guide Classes: Biguanide, Sulfonylurea, TZD, DPP-4 inhibitor, GLP-1 receptor agonist, SGLT2i,
Medication Guide Classes ... #Medications #pharmacology ... #comparison #table ... #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Autosomal recessive mutation ... enzyme 21-OHase causes ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
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