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PUBMED FOR HANDHELDS

Journal Abstract Search


266 related items for PubMed ID: 7959677

  • 1. Molecular biology of hypophosphataemic rickets and oncogenic osteomalacia.
    Rowe PS.
    Hum Genet; 1994 Nov; 94(5):457-67. PubMed ID: 7959677
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  • 4. The role of abnormal vitamin D metabolism in X-linked hypophosphatemic rickets and osteomalacia.
    Drezner MK.
    Adv Exp Med Biol; 1984 Nov; 178():399-404. PubMed ID: 6542302
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  • 5. The role of the PHEX gene (PEX) in families with X-linked hypophosphataemic rickets.
    Rowe PS.
    Curr Opin Nephrol Hypertens; 1998 Jul; 7(4):367-76. PubMed ID: 9690034
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  • 6. X-linked hypophosphatemia.
    Meyer RA, Conway WF, Chan JC.
    Semin Nephrol; 1989 Mar; 9(1):56-61. PubMed ID: 2662303
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  • 7. The molecular background to hypophosphataemic rickets.
    Rowe PS.
    Arch Dis Child; 2000 Sep; 83(3):192-4. PubMed ID: 10952628
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  • 11. Inherited forms of rickets and osteomalacia.
    Thakker RV, O'Riordan JL.
    Baillieres Clin Endocrinol Metab; 1988 Feb; 2(1):157-91. PubMed ID: 2900631
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  • 12. [From gene to disease; hypophosphataemic rickets and the PHEX gene].
    Jansen M, van Dael CM, Verrijn Stuart AA, van der Hout AH, Rump P.
    Ned Tijdschr Geneeskd; 2006 Jun 24; 150(25):1390-4. PubMed ID: 16841587
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  • 13. Pathogenesis of rickets and osteomalacia in familial hypophosphataemia.
    Condon JR, Nassim JR, Rutter A.
    Arch Dis Child; 1971 Jun 24; 46(247):269-72. PubMed ID: 5090660
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  • 15. [Adult-onset sex-linked familial hypophosphatemic osteomalacia].
    Radó J, Haris A, Szebenyi B.
    Orv Hetil; 1997 Jun 29; 138(26):1683-8. PubMed ID: 9289682
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  • 18. Clinical disorders of renal tubular phosphate transport.
    Levi M.
    Am J Med Sci; 1989 Sep 29; 298(3):194-205. PubMed ID: 2552801
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  • 19. Abnormal regulation of renal vitamin D catabolism by dietary phosphate in murine X-linked hypophosphatemic rickets.
    Tenenhouse HS, Jones G.
    J Clin Invest; 1990 May 29; 85(5):1450-5. PubMed ID: 2332500
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  • 20. Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.
    Jones AO, Tzenova J, Frappier D, Crumley MJ, Roslin NM, Kos CH, Tieder M, Langman CB, Proesmans W, Carpenter TO, Rice A, Anderson D, Morgan K, Fujiwara TM, Tenenhouse HS.
    J Am Soc Nephrol; 2001 Mar 29; 12(3):507-514. PubMed ID: 11181798
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