17 results
diagnosis differential pharmacology diabetes management treatment dermatology genetics hepatology hyponatremia insulin pathophysiology 21hydroxylasedeficiency 21ohd acromegaly addiction agonists anthracycline ascites based
Estimating the Total Daily Dose (TDD) of Insulin: Weight-Based Dosing TDD in units of insulin = N
: Weight-Based Dosing ... #TDD #Insulin #dosing ... #pharmacology #endocrinology ... #diabetes #DM2
DPP4 Inhibitors - Normal and Renal Dosing Increase Incretins (GLP-I & GIP) -> Stimulates Insulin, Inhibits Glucagon
Normal and Renal Dosing ... Inhibitors #Renal #Dosing ... Management #Diabetes #DM2 ... #Endocrinology
Erythroderma - Diagnostic Algorithm. Pathophysiology: 1) Extensive cutaneous capillary dilation, results in widespread exfoliation of the
Erythroderma - Diagnostic Algorithm ... Causes: 1) Exfoliative ... Histamine 4) Skin-homing ... Erythroderma #Nikolsky #Algorithm
Causes of Hyponatremia - Differential Diagnosis Algorithm Hypovolemia, UNa > 20: • Renal losses, Diuretic excess,
Causes of Hyponatremia ... Differential Diagnosis Algorithm ... deficiency, Salt-losing ... Differential #Diagnosis #Algorithm ... #Causes #nephrology
Causes of Pleural Effusion - Differential Diagnosis Algorithm Transudate - Hydrostatic • Congestive heart failure • Constrictive
Causes of Pleural ... Differential Diagnosis Algorithm ... syndrome • Protein-losing ... Pulmonary #Diagnosis #Algorithm ... #Hepatology #causes
Causes of Ascites - Differential Diagnosis Algorithm Portal Hypertension - Prehepatic: • Portal vein thrombosis • Splenic
Causes of Ascites ... Differential Diagnosis Algorithm ... Malnutrition • Protein-losing ... Differential #Diagnosis #Algorithm ... #Hepatology #causes
GLP-1 Agonists Adlyxin (Lixisenatide) Daily Bydureon (Exenatide ER) Weekly Ozempic (Semaglutide) Weekly Trulicity (Dulaglutide) Weekly Victoza (Liraglutide) Daily
#Pharmacology #Dosing ... #Diabetes #DM2 ... #Endocrinology
Duchenne Muscular Dystrophy (DMD) The term "Muscular dystrophy" refers to a group of inherited progressive muscle disorders.
Muscular Dystrophy (DMD ... defects in the gene coding ... brain. 1 in 3 cases ... MuscularDystrophy #DMD
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
mutation in CYP21A2 coding ... enzyme 21-OHase causes ... pathophysiology #genetics #endocrinology
Management of Hyponatremia Hypertonic Saline - Only indicated if patient has severe symptoms + Na < 125 Give
• Discuss with endocrinology ... about adding Tolvaptan ... SIADH — look for cause ... hourly • Identify Cause ... Hyponatremia #Management #algorithm
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