Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

Volumn 27, Issue 5, 2012, Pages 1729-1736

  Cochat, Pierre ^a   Hulton, Sally Anne ^b   Acquaviva, Cécile ^b   Danpure, Christopher J ^b   Daudon, Michel ^b   De Marchi, Mario ^b   Fargue, Sonia ^b   Groothoff, Jaap ^b   Harambat, Jérôme ^b   Hoppe, Bernd ^b   Jamieson, Neville V ^b   Kemper, Markus J ^b   Mandrile, Giorgia ^b   Marangella, Martino ^b   Picca, Stefano ^b   Rumsby, Gill ^b   Salido, Eduardo ^b   Straub, Michael ^b   van Woerden, Christiaan S ^b   OxalEurope, ^b  

^a UNIVERSITÉ LYON 1   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE GLYOXYLATE AMINOTRANSFERASE; ALANINE-GLYOXYLATE TRANSAMINASE; AMINOTRANSFERASE; CITRATE POTASSIUM; OXALIC ACID DERIVATIVE; PYRIDOXINE;

ARTICLE; ECHOGRAPHY; FLUID THERAPY; GENETIC SCREENING; GENETICS; HUMAN; KIDNEY; KIDNEY TRANSPLANTATION; METABOLISM; MUTATION; OXALOSIS 1; PRACTICE GUIDELINE;

FLUID THERAPY; GENETIC TESTING; HUMANS; HYPEROXALURIA, PRIMARY; KIDNEY; KIDNEY TRANSPLANTATION; MUTATION; OXALATES; POTASSIUM CITRATE; TRANSAMINASES; VITAMIN B 6;

EID: 84865960907     PISSN: None     EISSN: 14602385     Source Type: Journal    
DOI: 10.1093/ndt/gfs078     Document Type: Article

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