Primary hyperoxaluria: Liver biopys or DNA analysis? [4]

Pediatric Nephrology

Volumn 18, Issue 5, 2003, Pages 485-

  Tasic, Velibor ^a   Ristoska Bojkovska, Nadica ^a  

^a Medical School Skopje   (Macedonia)

Author keywords

DNA analysis; Glycolate; L Glycerate; Liver biopsy; Primary hyperoxaluria

Indexed keywords

CITRATE POTASSIUM; CREATININE; GLYCERIC ACID; OXALIC ACID; PYRIDOXINE;

CASE REPORT; CHILD; COLIC; CREATININE BLOOD LEVEL; DNA DETERMINATION; ECHOGRAPHY; EXON; HEMATURIA; HUMAN; INTRAVENOUS UROGRAPHY; KIDNEY SURGERY; LETTER; LIVER BIOPSY; MALE; NEPHROLITHIASIS; OXALOSIS 1; PRIORITY JOURNAL;

EID: 0038081075     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-003-1102-8     Document Type: Letter

References (2)

1. Milosevic D, Rinat C, Batinic D, Frishberg Y (2002) Genetic analysis - a diagnostic tool for primary hyperoxaluria type I. Pediatr Nephrol 17:896-898
2. Rumsby G, Sharma A, Cregeen DP, Solomon LR (2001) Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed? Nephrol Dial Transplant 16:1697-1699