An Acadian variant of Fanconi syndrome

Pediatric Nephrology

Volumn 22, Issue 10, 2007, Pages 1711-1715

  Wornell, Philip ^a   Crocker, John ^a   Wade, Andrew ^b   Dixon, Jason ^a   Acott, Philip ^a  

^a DALHOUSIE UNIVERSITY   (Canada)

^b UNIVERSITY OF CALGARY   (Canada)

Author keywords

Aminoaciduria; Chronic kidney disease; Hypophosphatemia; Renal tubular acidosis; Rickets proteinuria

Indexed keywords

ALKALI; CREATININE; PHOSPHATE; VITAMIN D;

ARTICLE; BONE DISEASE; CANADA; CHILD; CHILD GROWTH; CHRONIC KIDNEY DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; CREATININE CLEARANCE; DEMOGRAPHY; DIET SUPPLEMENTATION; FANCONI RENOTUBULAR SYNDROME; FOLLOW UP; HUMAN; HYPOPHOSPHATEMIA; IMMIGRANT; KIDNEY FUNCTION; KIDNEY TRANSPLANTATION; LUNG FIBROSIS; PATIENT REFERRAL; PRIORITY JOURNAL; PROTEINURIA; RICKETS; SCORING SYSTEM; SHORT STATURE; TREATMENT RESPONSE; VALGUS KNEE;

ADOLESCENT; ADULT; BIRTH WEIGHT; BODY WEIGHT; CANADA; CHILD; CHILD, PRESCHOOL; FANCONI ANEMIA; HUMANS; PROTEINURIA; RICKETS; VARIATION (GENETICS);

EID: 34548362113     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-007-0553-8     Document Type: Article

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