Gitelman's syndrome (Familial hypokalemia-hypomagnesemia)

Journal of Nephrology

Volumn 14, Issue 1, 2001, Pages 43-47

  Barakat, A J ^a   Rennert, O M ^a  

^a NONE   (United States)

Author keywords

Bartter's syndrome; Hypokalemia; Hypomagnesemia

Indexed keywords

CALCIUM; MAGNESIUM; MAGNESIUM SALT; SODIUM CHLORIDE; THIAZIDE DIURETIC AGENT;

ADOLESCENT; ARTICLE; BARTTER SYNDROME; CASE REPORT; CHROMOSOME 16Q; DIFFERENTIAL DIAGNOSIS; FAMILIAL DISEASE; GENE MUTATION; GENETIC CODE; GITELMAN SYNDROME; GROWTH; HENLE LOOP; HUMAN; HYPOCALCIURIA; HYPOKALEMIA; HYPOMAGNESEMIA; KIDNEY FUNCTION; LIFE EXPECTANCY; MAGNESIUM BLOOD LEVEL; MALE; PROGNOSIS; SODIUM TRANSPORT; URINARY EXCRETION;

BARTTER SYNDROME; CARRIER PROTEINS; CHILD; CHROMOSOMES, HUMAN, PAIR 16; DIAGNOSIS, DIFFERENTIAL; HUMANS; HYPOKALEMIA; KIDNEY DISEASES; MAGNESIUM; MALE; SODIUM CHLORIDE SYMPORTERS; SYMPORTERS; SYNDROME;

EID: 0035090306     PISSN: 11218428     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (34)

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2. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes
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4. A case of Gitelman's syndrome with chondrocalcinosis
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6. Luminal influences on potassium secretion: Chloride, sodium and thiazide diuretics
7. Possible discrimination of Gitelman's syndrome from Bartter's syndrome by renal clearance study: Report of two cases
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9. - by the thiazide-inhibitable transporter of the distal convoluted tubule in Gitelman's syndrome
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14. Bartter and related syndromes: The puzzle is almost solved
15. Renal magnesium wasting and hypocalciuria in chronic cis-platinum nephropathy in man
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19. The Na-(K)-Cl cotransporter family in the mammalian kidney: Molecular identification and function(s)
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28. Assignment of the genes encoding the human chloride channels, CLCNKA and CLCNKB, to 1P36 and of CLCN3 to 4q32-q33 by in situ hybridization
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30. + channel, ROMK
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