Early appearance of hypokalemia in Gitelman syndrome

Pediatric Nephrology

Volumn 25, Issue 10, 2010, Pages 2179-2182

  Tammaro, Fabiana ^a   Bettinelli, Alberto ^a   Cattarelli, Donatella ^b   Cavazza, Alessandra ^c   Colombo, Carla ^d   Syrén, Marie Louise ^e   Tedeschi, Silvana ^f   Bianchetti, Mario G ^g  

^a A MANZONI HOSPITAL   (Italy)

^b Gavardo Hospital   (Italy)

^c Spedali Riuniti ^*  (Italy)

^d SAN GERARDO HOSPITAL   (Italy)

^e UNIVERSITY OF MILAN   (Italy)

^f FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

^g UNIVERSITY OF BERN   (Switzerland)

Author keywords

Bartter syndrome; Gitelman syndrome; Hypokalemia; Hypomagnesemia; Preterm neonate

Indexed keywords

INDOMETACIN; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; SODIUM CHLORIDE COTRANSPORTER; SPHINGOLIPID ACTIVATOR PROTEIN 2;

ANAMNESIS; ARTICLE; BLOOD PRESSURE; CASE REPORT; CLCNKB GENE; EXON; FEMALE; FRAMESHIFT MUTATION; GENE; GENE MUTATION; GITELMAN SYNDROME; HUMAN; HYPERRENINEMIA; HYPOCHLOREMIA; HYPOKALEMIA; MALE; MISSENSE MUTATION; MOLECULAR BIOLOGY; NEWBORN; POTASSIUM EXCRETION; PREMATURITY; PRIORITY JOURNAL; SLC12A1 GENE; TWINS;

CHILD, PRESCHOOL; FEMALE; GITELMAN SYNDROME; HUMANS; HYPOKALEMIA; INFANT, NEWBORN; INFANT, PREMATURE; MALE; MUTATION; RECEPTORS, DRUG; SYMPORTERS;

EID: 77956231718     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-010-1575-1     Document Type: Article

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