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Journal Abstract Search

247 related items for PubMed ID: 17020415

  • 1. Hyperoxaluria and systemic oxalosis: current therapy and future directions.
    Bobrowski AE, Langman CB.
    Expert Opin Pharmacother; 2006 Oct; 7(14):1887-96. PubMed ID: 17020415
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  • 3. [Primary hyperoxaluria].
    Cochat P, Fargue S, Bacchetta J, Bertholet-Thomas A, Sabot JF, Harambat J.
    Nephrol Ther; 2011 Jul; 7(4):249-59. PubMed ID: 21636340
    [Abstract] [Full Text] [Related]

  • 4. Hyperoxaluria and systemic oxalosis: an update on current therapy and future directions.
    Beck BB, Hoyer-Kuhn H, Göbel H, Habbig S, Hoppe B.
    Expert Opin Investig Drugs; 2013 Jan; 22(1):117-29. PubMed ID: 23167815
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  • 5. Primary hyperoxaluria type 1: strategy for organ transplantation.
    Cochat P, Fargue S, Harambat J.
    Curr Opin Organ Transplant; 2010 Oct; 15(5):590-3. PubMed ID: 20733487
    [Abstract] [Full Text] [Related]

  • 6. Vitamin B6 resistant primary hyperoxaluria type I. Report of 5 cases.
    Streefland M, Donckerwolcke RA.
    Helv Paediatr Acta; 1989 Feb; 43(4):313-24. PubMed ID: 2708072
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  • 7. Primary hyperoxaluria.
    Scheinman JI.
    Miner Electrolyte Metab; 1994 Feb; 20(6):340-51. PubMed ID: 7783696
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  • 8. [Primary hyperoxaluria].
    Toussaint C, De Pauw L.
    Nephrologie; 1995 Feb; 16(6):399-406. PubMed ID: 8524446
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  • 10. [Primary hyperoxaluria].
    Ladefoged SD, Jørgensen HE.
    Ugeskr Laeger; 1989 Jul 17; 151(29):1856-9. PubMed ID: 2672487
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  • 12. Diagnosis and management of primary hyperoxaluria type 1 in infancy.
    Parekh RS, Smoyer WE, Bunchman TE.
    Pediatr Transplant; 1997 Aug 17; 1(1):48-54. PubMed ID: 10084787
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  • 14. [Inherited monogenic kidney stone diseases: recent diagnostic and therapeutic advances].
    Jungers P, Joly D, Blanchard A, Courbebaisse M, Knebelmann B, Daudon M.
    Nephrol Ther; 2008 Jul 17; 4(4):231-55. PubMed ID: 18499551
    [Abstract] [Full Text] [Related]

  • 15. Renal transplantation in a child with primary oxalosis.
    Casale AJ, Leichter HE, Sheth KJ, Segura AD, Lawson RK.
    Child Nephrol Urol; 1990 Jul 17; 10(2):103-6. PubMed ID: 2253246
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  • 16. Primary hyperoxaluria (type I): attempted treatment by combined hepatic and renal transplantation.
    Watts RW, Calne RY, Williams R, Mansell MA, Veall N, Purkiss P, Rolles K.
    Q J Med; 1985 Oct 17; 57(222):697-703. PubMed ID: 3909198
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  • 17. Primary hyperoxaluria: clinical course, diagnosis, and treatment after kidney failure.
    Raju DL, Cantarovich M, Brisson ML, Tchervenkov J, Lipman ML.
    Am J Kidney Dis; 2008 Jan 17; 51(1):e1-5. PubMed ID: 18155525
    [Abstract] [Full Text] [Related]

  • 18. [From gene to disease; primary hyperoxaluria type I caused by mutations in the AGXT gene].
    van Woerden CS, Groothof JW, Wanders RJ, Waterham HR, Wijburg FR.
    Ned Tijdschr Geneeskd; 2006 Jul 29; 150(30):1669-72. PubMed ID: 16922352
    [Abstract] [Full Text] [Related]

  • 19. Recurrence of crystalline nephropathy after kidney transplantation in APRT deficiency and primary hyperoxaluria.
    Bollée G, Cochat P, Daudon M.
    Can J Kidney Health Dis; 2015 Jul 29; 2():31. PubMed ID: 26380104
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  • 20. An update on primary hyperoxaluria.
    Hoppe B.
    Nat Rev Nephrol; 2012 Jun 12; 8(8):467-75. PubMed ID: 22688746
    [Abstract] [Full Text] [Related]

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