Genotype-phenotype correlations in normotensive patients with primary renal tubular hypokalemic metabolic alkalosis

Journal of Nephrology

Volumn 11, Issue 2, 1998, Pages 61-69

  Bettinelli, Alberto ^a,f   Vezzoli, Giuseppe ^b   Colussi, Giacomo ^c   Bianchetti, Mario Giovanni ^d   Sereni, Fabio ^a   Casari, Giorgio ^e  

^a Istituti Clinici di Perfezionamento   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c OSPEDALE NIGUARDA CA GRANDA   (Italy)

^d Abteilung fur Nephrologie   (Switzerland)

^e TELETHON INSTITUTE OF GENETICS AND MEDICINE TIGEM   (Italy)

^f Clinica Pediatrica   (Italy)

Author keywords

Bartter syndrome; Cleara nce studies; Furosemide test; Gitelman disease; Hypercalciuria; Hypocalciuria; Hypokalemia; Hypomagnesemia; Metabolic alkalosis; Nephrocalcinosis

Indexed keywords

BUMETANIDE; CALCIUM; CARRIER PROTEIN; CHLORIDE CHANNEL; CHLORIDE ION; DIURETIC AGENT; FUROSEMIDE; HYDROCHLOROTHIAZIDE; POTASSIUM; POTASSIUM CHANNEL; SODIUM ION; THIAZIDE DIURETIC AGENT;

BARTTER SYNDROME; CLINICAL FEATURE; GENOTYPE; GITELMAN SYNDROME; HUMAN; HYPERCALCIURIA; HYPOCALCIURIA; HYPOKALEMIA; HYPOMAGNESEMIA; KIDNEY CLEARANCE; KIDNEY TUBULE DISORDER; METABOLIC ALKALOSIS; MUTATION; PHENOTYPE; REVIEW;

ALKALOSIS; BARTTER SYNDROME; BLOOD PRESSURE; CHILD; CHILD, PRESCHOOL; GENOTYPE; HUMANS; HYPOKALEMIA; INFANT; INFANT, NEWBORN; KIDNEY FUNCTION TESTS; KIDNEY TUBULES; PHENOTYPE;

EID: 0031979678     PISSN: 11218428     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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