Gitelman's Syndrome in Pregnancy With Adverse Foetal Outcome: A Case Report. [PDF]
Najam R, Tomar Y, Singh M.
europepmc +1 more source
Successful living kidney donation from a patient with a Gitelman's syndrome. [PDF]
Darrat M +5 more
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Knowing the meaning of the words we use: Gitelman’s syndrome or Gitelman’s disease?
Víctor M. García-Nieto +2 more
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Anesthetic Challenges of an Adolescent Patient with Epidermolysis Bullosa and Gitelman's Syndrome Undergoing Posterior Spinal Fusion Surgery. [PDF]
Kiss EE, Chandran N, Alex G, Olomu P.
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Gitelman's Syndrome with Mental Retardation
A 56-year-old mentally retarded Japanese woman (intelligence quotient: 49) was admitted to our hospital with the chief complaints of headache, dizziness, vomiting, and lower limb paralysis. Laboratory tests showed severe hypokalemia, metabolic alkalosis, hypomagnesemia, and hypocalciuria. These findings suggested a diagnosis of Gitelman's syndrome (GS).
Rena, Morita +4 more
openaire +3 more sources
OBJECTIVE: Bartter's syndrome is a rare genetic disorder characterized by renal salt wasting, hypokalemia and metabolic alkalosis. CASE REPORT: A 32 years old male patient presented to casualty with complaints of generalised weakness and chest ...
A P, Ambali, J V, Bomman, Mulimani, M S
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Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent [PDF]
Gitelman syndrome is a renal tubular salt-wasting disorder characterized by hypokalemic metabolic alkalosis with hypomagnesemia and hypocalciuria. Patients occasionally have symptoms in childhood, while diagnosis is often in adulthood. It is inherited by
Ali Anarat +6 more
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Interleukin 18 function in atherosclerosis is mediated by the interleukin 18 receptor and the Na-Cl co-transporter [PDF]
Interleukin-18 (IL18) participates in atherogenesis through several putative mechanisms1, 2. Interruption of IL18 action reduces atherosclerosis in mice3, 4.
Bindels, René +26 more
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A Case of Gitelman`s Syndrome in Obese Patient Taking Diuretics for the Purpose of Weight Reduction [PDF]
Gitelman 셲 syndrome is a primary renal tubular disorder characterized by chronic hypokalemia, hypomagnesemia, metabolic alkalosis of renal origin, hypocalciuria with normocalcemia, hyperreninemic hyperaldosteronism, increased excretion of urinary ...
諛뺤쥌�꽍, �븞泥좎슦
core
Genetic renal Dyskalemias: old syndromes, new genes [PDF]
Detailed formal protocol with illustrations and extensive bibliography.UT Southwestern--Internal ...
Alpern, Robert J.
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