201 results
diagnosis neurology algorithm management hyponatremia treatment comparison hematology hypokalemia low ophthalmology potassium signs symptoms cardiology clinical metabolic classification sodium syndromes
Localization of Renal Tubular Defects Fanconi Syndrome: Proximal tubule Bartter Syndrome: Thick ascending loop of Henle Gitelman Syndrome: Distal
Renal Tubular Defects ... Fanconi Syndrome ... Localization #Nephron #Defects ... #Pathophysiology ... #Nephrology
Isocoria - Pupillary Defects - Differential Diagnosis Algorithm Relative Afferent Pupil Defect • Optic Neuritis • Ischemic
- Differential ... Afferent Pupil Defect ... Midbrain (Parinaud's Syndrome ... #Differential # ... Diagnosis #Algorithm #Causes
Nephrotic Syndrome - Primary vs Secodary - Differential Diagnosis Algorithm #Nephrotic #Syndrome #Differential #Diagnosis #Algorithm #Primary #Secondary
Nephrotic Syndrome ... #Nephrotic #Syndrome ... #Differential # ... Primary #Secondary #Nephrology ... #Causes
Initial Clinical and Laboratory Data Base for Defining Major Syndromes in Nephrology #Major #Syndromes #Nephrology #Diagnosis #Workup
Defining Major Syndromes ... in Nephrology ... #Major #Syndromes ... #Workup #Differential ... #Table
Non-cirrhotic Hyperammonemia - Differential Diagnosis Framework Hematologic & Vascular: • Multiple myeloma & Acute leukemia (plasma cells
Hyperammonemia - Differential ... Infections: • Urease-producing ... retention Unmasked Urea ... Cycle Defects ... #Diagnosis #Pathophysiology
Clues to Differential Diagnosis of Central Cyanosis: Onset of cyanosis, Clubbing, Secondary erythrocytosis, Auscultation, X-ray, Echocardiography,
Clues to Differential ... Cyanotic heart defect ... #Cyanosis #Differential ... Central #Cardiology #Causes ... #Table #Comparison
Reflex Testing - Causes of Hyporeflexia and Hyperreflexia Focal Hyporeflexia: • Radiculopathy, Mononeuropathy, Polyneuropathy, Acute stroke,
Guillain-Barré syndrome ... Hyperthyroidism, Serotonin syndrome ... #differential # ... diagnosis #table ... #neurology
Schematic representation of the major sources of ammonia production and its excretory pathway (GI = gastrointestinal,
- Inherited Urea ... of ammonia: - Urease ... rare): - Reye syndrome ... deficiency #Ammonia #Pathophysiology ... Hyperammonemia #Differential
Hypomagnesemia - Etiologies by Mechanism Decreased GI Uptake - Poor dietary intake (particularly common in alcoholics)
- Genetic defects ... - Hungry bones syndrome ... Hypomagnesemia #Differential ... Low #Magnesium #Table ... Classification #Causes
Inherited Defects in Kidney Tubule Epithelial Cells Renal glucosuria - Na+-dependent glucose cotransporter Cystinuria - Amino acid transporter Bartter
Inherited Defects ... Epithelial #Inherited #Defects ... #Kidney #Nephrology ... #Diagnosis #Differential ... #Table
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