Hypokalemia and hypomagnesemia of hereditary renal tubular origin. Bartter and Gitelman syndromes;Ipopotassiemie ed ipomagnesiemie di origine renale tubulare. Le sindromi di Bartter e di Gitelman

Acta Biomedica de l'Ateneo Parmense

Volumn 74, Issue 3, 2003, Pages 163-167

  Bettinelli, Alberto ^a,b   Tedeschi, Silvana ^c  

^a A MANZONI HOSPITAL   (Italy)

^b Clinica Pediatrica De Marchi   (Italy)

^c PARKINSON INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ELECTROLYTE; INDOMETACIN; MAGNESIUM; POTASSIUM CHLORIDE; PROSTAGLANDIN SYNTHASE INHIBITOR; ROFECOXIB; SODIUM CHLORIDE; SPIRONOLACTONE;

BARTTER SYNDROME; CLINICAL FEATURE; CONFERENCE PAPER; GASTROINTESTINAL SYMPTOM; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC HETEROGENEITY; GITELMAN SYNDROME; HISTORY OF MEDICINE; HUMAN; HYDRAMNIOS; HYPOCALCIURIA; HYPOKALEMIA; HYPOMAGNESEMIA; KIDNEY CALCIFICATION; KIDNEY TUBULE DISORDER; MOLECULAR GENETICS; PATHOGENESIS; POTASSIUM DEFICIENCY; SKIN INFLAMMATION;

BARTTER SYNDROME; HUMANS; HYPOKALEMIA; MAGNESIUM DEFICIENCY; PORTRAITS; RENAL TUBULAR TRANSPORT, INBORN ERRORS;

EID: 1542410509     PISSN: 03924203     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (14)

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