Presymptomatic detection of familial juvenile hyperuricaemic nephropathy in children

Pediatric Nephrology

Volumn 12, Issue 5, 1998, Pages 357-364

  McBride, Mary B ^a   Rigden, Sue ^a   Haycock, George B ^a   Dalton, Neil ^a   Van't Hoff, William ^b   Rees, Lesley ^b   Raman, G Venkat ^c   Moro, Fernando ^c   Ogg, Chisholm S ^a   Cameron, J Stewart ^a   Simmonds, H Anne ^a,d  

^a KING'S COLLEGE LONDON   (United Kingdom)

^b HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^c ST MARY S HOSPITAL   (United Kingdom)

^d GUY S HOSPITAL   (United Kingdom)

Author keywords

Allopurinol; Dominant genetic disease; Familial renal disease; Fractional urate clearance; Hyperuricaemia; Juvenile gout

Indexed keywords

ALLOPURINOL; URATE; URIC ACID;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DOMINANT INHERITANCE; FEMALE; GLOMERULUS FILTRATION RATE; GOUT; HUMAN; HYPERURICEMIA; LESCH NYHAN SYNDROME; MALE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; GOUT; HUMANS; KIDNEY DISEASES; KIDNEY FAILURE, CHRONIC; MALE; PEDIGREE; URIC ACID;

EID: 7344245989     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004670050466     Document Type: Article

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