Primary molecular deficiencies and secondary adaptations in bartter and gitelman syndromes;Altérations moléculaires primaires et troubles biologiques secondaires des syndromes de bartter et de gitelman

Archives de Pediatrie

Volumn 9, Issue 4, 2002, Pages 406-416

  Deschenes G ^a   Feldmann, D ^a   Doucet, A ^b  

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b CNRS   (France)

Author keywords

Bartter's disease; Genetics, renal tubulan transplant, inborn errors; Molecular biology

Indexed keywords

ALDOSTERONE; CALCIUM; MAGNESIUM; PROSTAGLANDIN; SODIUM;

BARTTER SYNDROME; BLOOD PRESSURE; CALCIUM EXCRETION; CLINICAL FEATURE; GITELMAN SYNDROME; HENLE LOOP; HUMAN; HYPERALDOSTERONISM; HYPERTROPHY; HYPOKALEMIA; JUXTAGLOMERULAR APPARATUS; KIDNEY COLLECTING TUBULE; KIDNEY DISTAL TUBULE; MAGNESIUM EXCRETION; METABOLIC ALKALOSIS; NONHUMAN; PATHOPHYSIOLOGY; PROSTAGLANDIN SYNTHESIS; REGULATORY MECHANISM; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; REVIEW; SODIUM ABSORPTION;

EID: 17944384938     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(01)00801-6     Document Type: Short Survey

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