Magnesium supplementation in Gitelman syndrome

Gitelman's variant of Barter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na–Cl cotransporter

David B. Simon, Carol Nelson‐Williams, Margaret J. Bia et al. · Nature Genetics · 1996 · 1.2K citations

Physiology, Pathology, Hypokalaemic Alkalosis +3

Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

Alberto Bettinelli, Mario G. Bianchetti, Éric Girardin et al. · The Journal of Pediatrics · 1992 · 346 citations

Hypertonicity, Urology, Electrolyte Disorder +8

Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome.

Nadia Mastroianni, Alberto Bettinelli, Mario G. Bianchetti et al. · PubMed · 1996 · 151 citations

Molecular Cloning, Expression Pattern, and Chromosomal Localization of the Human Na–Cl Thiazide-Sensitive Cotransporter (SLC12A3)

Nadia Mastroianni, Maurizio De Fusco, Massimo Zollo et al. · Genomics · 1996 · 127 citations

Molecular Physiology, Signal Transduction, Chromosomal Localization +11

Transtubular potassium concentration gradient: a useful test to estimate renal aldosterone bio-activity in infants and children

Juan Rodr�guez-Soriano, M Ubetagoyena, Alfredo Vallo · Pediatric Nephrology · 1990 · 88 citations

Hypertonicity, Urology, Renal Function +11