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Gitelman syndrome.
Orphanet J Rare Dis. 2008 Jul 30;3:22. doi: 10.1186/1750-1172-3-22.
Orphanet J Rare Dis. 2008.
PMID: 18667063
Free PMC article.
Review.
Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalemic metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. ...
Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalemic metabo …
Gitelman's syndrome (familial hypokalemia-hypomagnesemia).
Barakat AJ, Rennert OM.
Barakat AJ, et al.
J Nephrol. 2001 Jan-Feb;14(1):43-7.
J Nephrol. 2001.
PMID: 11281344
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Familial hypokalemia-hypomagnesemia or Gitelman's syndrome: a further case.
Zarraga Larrondo S, Vallo A, Gainza J, Muñiz R, Garcia Erauzkin G, Lampreabe I.
Zarraga Larrondo S, et al.
Nephron. 1992;62(3):340-4. doi: 10.1159/000187070.
Nephron. 1992.
PMID: 1436349
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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain.
Lemmink HH, Knoers NV, Károlyi L, van Dijk H, Niaudet P, Antignac C, Guay-Woodford LM, Goodyer PR, Carel JC, Hermes A, Seyberth HW, Monnens LA, van den Heuvel LP.
Lemmink HH, et al.
Kidney Int. 1998 Sep;54(3):720-30. doi: 10.1046/j.1523-1755.1998.00070.x.
Kidney Int. 1998.
PMID: 9734597
Free article.
Gitelman syndrome (familial hypokalemia-hypomagnesemia syndrome) is an autosomal recessive inherited renal disorder characterized by defective tubular reabsorption of magnesium and potassium. ...
Gitelman syndrome (familial hypokalemia-hypomagnesemia syndrome) is an autosomal recessive inherited renal disorder cha …
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