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diagnosis management differential neurology algorithm causes hrs alkalosis hypokalemia metabolic rheumatology syndromes barre chloride defects guillain medications pharmacology potassium table
Pathophysiology of hepatorenal syndrome (HRS) doi: 10.1136/bmj.m2687 #hepatorenal #syndrome #HRS #Pathophysiology #nephrology
Pathophysiology ... of hepatorenal syndrome ... #syndrome #HRS ... #Pathophysiology ... #nephrology
HepatoRenal Syndrome - Pathophysiology Dr. Edgar V. Lerma @edgarvlermamd - Nephrology Secrets https://amzn.to/34t5DgJ #HRS #HepatoRenal #Syndrome #Pathophysiology #Diagnosis
HepatoRenal Syndrome ... - Pathophysiology ... edgarvlermamd - Nephrology ... #Syndrome #Pathophysiology ... #Diagnosis #Nephrology
Hepatorenal Syndrome - Pathophysiology - Dr. Eric Strong @DrEricStrong - Strong Medicine https://www.youtube.com/c/EricsMedicalLectures/ #HRS #Hepatorenal #Syndrome #Pathophysiology #nephrology
Hepatorenal Syndrome ... - Pathophysiology ... EricsMedicalLectures/ #HRS #Hepatorenal ... #Syndrome #Pathophysiology ... #nephrology
Localization of Renal Tubular Defects Fanconi Syndrome: Proximal tubule Bartter Syndrome: Thick ascending loop of Henle Gitelman Syndrome: Distal
loop of Henle Gitelman ... Syndrome: Distal ... Fanconi #Bartter #Gitelman ... Nephron #Defects #Pathophysiology ... #Nephrology
Pharmacological Treatment of Hepatorenal Syndrome (HRS) Midodrine - Alpha agonist incr blood pressure incr renal perfusion pressure
Pharmacological Treatment ... of Hepatorenal ... Syndrome (HRS) ... #Syndrome #Nephrology ... #Medications #Treatment
Gitelman Syndrome Pathophysiology Gitelman Syndrome is a rare autosomal recessive salt-losing tubulopathy with a prevalence of 1-
Gitelman Syndrome ... Pathophysiology ... Gitelman Syndrome ... #Syndrome #Pathophysiology ... #nephrology #diagnosis
Hepatorenal Syndrome Treatment Volume expansion: • Albumin (typical dose = 1g/kg on day 1 +/- day
Hepatorenal Syndrome ... Treatment Volume ... EricsMedicalLectures/ #Hepatorenal ... #Syndrome #Treatment ... management #HRS #nephrology
Primary Metabolic Alkalosis - Differential Diagnosis Algorithm Volume Depleted 2° hyperaldosteronism • Low Urine Cl-: Vomiting, NGT
NGT suction, Low Cl ... • High Urine Cl ... , Gitelman Syndrome ... , Liddle syndrome ... Diagnosis #Algorithm #nephrology
Primary Metabolic Alkalosis - Differential Diagnosis Algorithm Volume Depleted - 2° hyperaldosteronism • Low Urine Cl-: Vomiting,
NGT suction, Low Cl ... • High Urine Cl ... , Gitelman Syndrome ... , Liddle syndrome ... Diagnosis #Algorithm #Nephrology
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
transporter Bartter syndrome ... ascending limb Gitelman ... syndrome - Thiazide-sensitive ... tubule Liddle syndrome ... Defects #Kidney #Nephrology
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