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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

315 related items for PubMed ID: 8685551

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  • 10. Genetic basis of primary hyperoxaluria type II.
    Webster KE, Cramer SD.
    Mol Urol; 2000; 4(4):355-64. PubMed ID: 11156703
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  • 11. [Oxalosis].
    Cordonnier C, Noel C, Gosselin B.
    Ann Pathol; 1995; 15(6):415-23. PubMed ID: 8720837
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  • 12. L-glyceric aciduria. A new genetic variant of primary hyperoxaluria.
    Williams HE, Smith LH.
    N Engl J Med; 1968 Feb 01; 278(5):233-8. PubMed ID: 5635456
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  • 13. Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment.
    Cochat P, Hulton SA, Acquaviva C, Danpure CJ, Daudon M, De Marchi M, Fargue S, Groothoff J, Harambat J, Hoppe B, Jamieson NV, Kemper MJ, Mandrile G, Marangella M, Picca S, Rumsby G, Salido E, Straub M, van Woerden CS, OxalEurope.
    Nephrol Dial Transplant; 2012 May 01; 27(5):1729-36. PubMed ID: 22547750
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  • 15. [Massive hyperoxaluria].
    Barbey F, Cachat F, Nguyen QV, Rotman S, Burnier M, Daudon M.
    Rev Med Suisse Romande; 2004 Aug 01; 124(8):477-82. PubMed ID: 15495471
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  • 16. Effects of alanine:glyoxylate aminotransferase variants and pyridoxine sensitivity on oxalate metabolism in a cell-based cytotoxicity assay.
    Fargue S, Knight J, Holmes RP, Rumsby G, Danpure CJ.
    Biochim Biophys Acta; 2016 Jun 01; 1862(6):1055-62. PubMed ID: 26854734
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  • 17. Strategies for the prenatal diagnosis of primary hyperoxaluria type 1.
    Danpure CJ, Rumsby G.
    Prenat Diagn; 1996 Jul 01; 16(7):587-98. PubMed ID: 8843467
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  • 19. Initial manifestation of primary hyperoxaluria type I in adults-- recognition, diagnosis, and management.
    Kuiper JJ.
    West J Med; 1996 Jan 01; 164(1):42-53. PubMed ID: 8779202
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  • 20. Primary hyperoxaluria type 1: clinical manifestations in infancy and prenatal diagnosis.
    Illum N, Lavard L, Danpure CJ, Horn T, AErenlund Jensen H, Skovby F.
    Child Nephrol Urol; 1992 Jan 01; 12(4):225-7. PubMed ID: 1473096
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