Primary hyperoxaluria type 2 in children

Pediatric Nephrology

Volumn 17, Issue 8, 2002, Pages 597-601

  Johnson, Sally A ^a   Rumsby, Gill ^b   Cregen, David ^b   Hulton, Sally Anne ^a  

^a BIRMINGHAM CHILDREN S HOSPITAL NHS FOUNDATION TRUST   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON HOSPITALS   (United Kingdom)

Author keywords

Glyoxylate reductase hydroxypyruvate reductase; Nephrolithiasis; Oxalate; Primary hyperoxaluria; Primary hyperoxaluria type 2; Urinary glycerate

Indexed keywords

DNA; GLYCERIC ACID; HYDROXYPYRUVATE REDUCTASE; OXALIC ACID;

ADOLESCENT; AGE; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COHORT ANALYSIS; CONTROLLED STUDY; DNA DETERMINATION; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENETIC LINKAGE; GLOMERULUS FILTRATION RATE; HEMATURIA; HOMOZYGOSITY; HUMAN; INFANT; KIDNEY CALCIFICATION; KIDNEY FUNCTION; LITHOTOMY; LITHOTRIPSY; MALE; NEPHROLITHIASIS; NUCLEOTIDE SEQUENCE; OXALOSIS; PREVALENCE; PRIORITY JOURNAL; URINARY TRACT INFECTION; URINE LEVEL;

ADOLESCENT; CALCIUM; CHILD; CHILD, PRESCHOOL; CREATININE; DNA; FEMALE; FOLLOW-UP STUDIES; HUMANS; HYPEROXALURIA, PRIMARY; INFANT; KIDNEY DISEASES; LEUKOCYTES; LINKAGE (GENETICS); MALE; MUTATION; RETROSPECTIVE STUDIES;

EID: 0036958667     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-002-0858-6     Document Type: Article

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