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Literature
1.
go back to reference Milosevic D, Rinat C, Batinic D, Frishberg Y (2002) Genetic analysis—a diagnostic tool for primary hyperoxaluria type I. Pediatr Nephrol 17:896–898CrossRefPubMed Milosevic D, Rinat C, Batinic D, Frishberg Y (2002) Genetic analysis—a diagnostic tool for primary hyperoxaluria type I. Pediatr Nephrol 17:896–898CrossRefPubMed
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go back to reference Rumsby G, Sharma A, Cregeen DP, Solomon LR (2001) Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed? Nephrol Dial Transplant 16:1697–1699PubMed Rumsby G, Sharma A, Cregeen DP, Solomon LR (2001) Primary hyperoxaluria type 2 without L-glycericaciduria: is the disease under-diagnosed? Nephrol Dial Transplant 16:1697–1699PubMed
Metadata
Title
Primary hyperoxaluria: liver biopsy or DNA analysis?
Authors
Velibor Tasic
Nadica Ristoska-Bojkovska
Publication date
01-05-2003
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 5/2003
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-003-1102-8

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