Chloride and sodium renal tubular handling in Dent's disease [1]

Pediatric Nephrology

Volumn 20, Issue 8, 2005, Pages 1198-1199

  Antón Gamero, Montserrat ^a   Claverie Martín, Félix ^b   García Nieto, Víctor ^b   Vela Enríquez, Francisco ^a   García Martínez, Elena ^a   Pérez Navero, J Luis ^a  

^a HOSPITAL UNIVERSITARIO REINA SOFÍA   (Spain)

^b HOSPITAL UNIVERSITARIO NUESTRA SEÑORA DE CANDELARIA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; CHLORIDE CHANNEL; SODIUM;

CASE REPORT; CLINICAL FEATURE; CREATININE CLEARANCE; DENT DISEASE; ELECTROLYTE BALANCE; ELECTROLYTE TRANSPORT; GENE FUNCTION; GENE INACTIVATION; GENE MUTATION; HUMAN; HYPERCALCIURIA; KIDNEY CALCIFICATION; KIDNEY CLEARANCE; KIDNEY DISEASE; KIDNEY FAILURE; KIDNEY TUBULE FUNCTION; LETTER; LOADING TEST; NEPHROLITHIASIS; PATHOGENESIS; PRIORITY JOURNAL; PROTEINURIA; RICKETS; SODIUM ABSORPTION; URINE OSMOLALITY; URINE VOLUME; WATER ABSORPTION;

CALCIUM; CHLORIDE CHANNELS; CHLORIDES; GENETIC DISEASES, X-LINKED; HUMANS; KIDNEY DISEASES; KIDNEY FAILURE; KIDNEY TUBULES; MUTATION; NEPHROCALCINOSIS; PROTEINURIA; SODIUM;

EID: 22344456810     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-005-1875-z     Document Type: Letter

References (8)

1. Thakker RV (2000) Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis. Kidney Int 57:787-793 1:CAS:528:DC%2BD3cXktFGgsbw%3D
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3. Rodriguez-Soriano J (1998) Bartter and related syndromes: The puzzle is almost solved. Pediatr Nephrol 12:315-327 1:STN:280:DyaK1czhvVSksw%3D%3D
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7. Carballo-Trujillo I, Garcia-Nieto V, Moya-Angeler FJ, Antón-Gamero M, Loris C, Méndez-Alvarez S, Claverie-Martin F (2003) Novel truncating mutations in the ClC-5 chloride channel gene in patients with Dent's disease. Nephrol Dial Transplant 18:717-723 1:CAS:528:DC%2BD3sXit1yru7Y%3D
8. Claverie-Martin F, González-Acosta H, Flores C, Antón-Gamero M. García-Nieto V (2003) De novo insertion of an Alu sequence in the coding region of the CLCN5 gene results in Dent's disease. Hum Genet 113:480-485 1:CAS:528:DC%2BD3sXot1Orsrs%3D