Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalcuria (Gitelman's syndrome)-Reference-Cited by-同舟云学术

Genetic heterogeneity in tubular hypomagnesemia-hypokalemia with hypocalcuria (Gitelman's syndrome)

Published:1995-02 Issue:2 Volume:47 Page:547-551
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Bettinelli Alberto,Bianchetti Mario Giovanni,Borella Paola,Volpini Elena,Metta Maria Gabriella,Basilico Elena,Selicorni Angelo,Bargellini Annamaria,Grassi Maria Rosa

Publisher

Elsevier BV

Subject

Nephrology

Reference20 articles.

1. The pathogenetic spectrum of Bartter's syndrome;Stein;Kidney Int,1985

2. Bartter's syndrome due to a defect in salt reabsorption in the distal convolute tubule;Uribarri;Nephron,1985

3. Bartter's syndrome. Evidence suggesting a distal tubular defect in a hypocalciuric variant of the syndrome;Sutton;Miner Electrol Metab,1992

4. A new familial disorder characterized by hypokalemia and hypomagnesemia;Gitelman;Trans Assoc Am Phys,1966

5. Hypomagnesaemia of hereditary renal origin;Rodriguez-Soriano;Pediatr Nephrol,1987

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1. Heart’s Dangerous Symphony: Torsade De Pointes Unleashed by Gitelman Syndrome-Induced Hypomagnesemia;Cureus;2023-08-31

2. A novel SLC12A3 gene homozygous mutation of Gitelman syndrome in an Asian pedigree and literature review;Journal of Endocrinological Investigation;2015-08-11

3. Identification of two novel mutations inSLC12A3gene in two Chinese pedigrees with Gitelman syndrome and review of literature;Clinical Endocrinology;2015-06-15

4. Gitelman syndrome DD thiazide diuretics abuse;Open Medicine;2014-06-01

5. Clinical Severity of Gitelman Syndrome Determined by Serum Magnesium;American Journal of Nephrology;2014