Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome

Pediatric Nephrology

Volumn 10, Issue 5, 1996, Pages 551-554

  Károlyi, Lothar ^a   Ziegler, Andreas ^a   Ollak, Martin ^b   Fischbach, Michael ^c   Grzeschik, Karl Heinz ^a   Koch, Manuela C ^a   Seyberth, Hannsjörg W ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

^c HÔPITAL DE HAUTEPIERRE   (France)

Author keywords

Bartter's syndrome; Gitelman's syndrome; Hyperprostaglandin E syndrome; Hypokalemic tubular disorder; Na Cl cotransport; Thiazides

Indexed keywords

DNA MARKER; PROSTAGLANDIN E;

ADOLESCENT; ADULT; ARTICLE; BARTTER SYNDROME; BIOCHEMISTRY; CHILD; CHLORIDE TRANSPORT; CHROMOSOME 16Q; CLINICAL FEATURE; DNA POLYMORPHISM; FEMALE; GENE LOCUS; GENE MUTATION; GENETIC DISORDER; GENETIC LINKAGE; GITELMAN SYNDROME; HUMAN; HUMAN CELL; HYPOCALCIURIA; HYPOKALEMIA; HYPOMAGNESEMIA; INFANT; KIDNEY TUBULE DISORDER; MAJOR CLINICAL STUDY; MALE; METABOLIC ALKALOSIS; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; SODIUM TRANSPORT;

ADOLESCENT; ADULT; BARTTER SYNDROME; CALCIUM; CHILD; CHILD, PRESCHOOL; FEMALE; HUMANS; HYPOKALEMIA; INFANT; KIDNEY DISEASES; KIDNEY TUBULES; LINKAGE (GENETICS); MAGNESIUM; MALE; SYNDROME;

EID: 0029778992     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050158     Document Type: Article

References (22)

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