Hereditary hyperuricemia and renal disease

Seminars in Nephrology

Volumn 25, Issue 1, 2005, Pages 9-18

  Cameron, J Stewart ^a,b   Simmonds, H Anne ^a  

^a GUY S HOSPITAL   (United Kingdom)

^b Elm Bank   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALI; ALLOPURINOL; AZATHIOPRINE; BENZBROMARONE; HYPOXANTHINE PHOSPHORIBOSYLTRANSFERASE; OXIPURINOL; PURINE DERIVATIVE; RASBURICASE; RIBOSEPHOSPHATE PYROPHOSPHOKINASE; URIC ACID;

AUTOSOMAL DOMINANT DISORDER; CLINICAL FEATURE; CORRELATION ANALYSIS; ENZYME ACTIVITY; ENZYME DEFICIENCY; FLUID INTAKE; GENE MUTATION; GENETIC DISORDER; GENETIC PREDISPOSITION; GLYCOGEN STORAGE DISEASE TYPE 1; HEMIZYGOTE; HUMAN; HYPERURICEMIA; KIDNEY DISEASE; KIDNEY FAILURE; LESCH NYHAN SYNDROME; MEDULLARY SPONGE KIDNEY; NEPHRONOPHTHISIS; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; PROTEIN EXPRESSION; PROTEIN SECRETION; PURINE SYNTHESIS; REVIEW; SEX LINKAGE; SIDE EFFECT; STONE FORMATION; URIC ACID BLOOD LEVEL; X CHROMOSOME LINKAGE;

EID: 12344275848     PISSN: 02709295     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.semnephrol.2004.09.003     Document Type: Article

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