Gitelman's syndrome: A pathophysiological and clinical update

Endocrine

Volumn 41, Issue 1, 2012, Pages 53-57

  Nakhoul, Farid ^a,b   Nakhoul, Nakhoul ^a   Dorman, Evgenia ^c   Berger, Liron ^c   Skorecki, Karl ^c   Magen, Daniella ^c  

^a Baruch Padeh Poryia Medical Center   (Israel)

^b BAR ILAN UNIVERSITY   (Israel)

^c TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

Author keywords

Gitelman's syndrome; Hypokalemia hypomagnesemia

Indexed keywords

CALCIUM; CREATININE; MAGNESIUM; POTASSIUM; SODIUM CHLORIDE COTRANSPORTER;

ADULT; CALCIUM URINE LEVEL; CASE REPORT; CHEMICAL ANALYSIS; CLINICAL FEATURE; CREATININE URINE LEVEL; DIET SUPPLEMENTATION; EXON; GENE; GENE MUTATION; GENETIC ANALYSIS; GITELMAN SYNDROME; HETEROZYGOSITY; HETEROZYGOTE DETECTION; HUMAN; HYPOKALEMIA; HYPOMAGNESEMIA; INTRON; MALE; METABOLIC ALKALOSIS; MUSCLE CRAMP; MUSCLE WEAKNESS; MUTATIONAL ANALYSIS; NEUROLOGIC EXAMINATION; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; SLC12A3 GENE; TETANY;

EID: 84862668202     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-011-9556-0     Document Type: Review

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