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Journal Abstract Search

365 related items for PubMed ID: 17906414

  • 1. [Hypophosphatemic rickets/osteomalacia. - Mainly on patients with PHEX mutations -].
    Hasegawa Y, Miyamoto J.
    Clin Calcium; 2007 Oct; 17(10):1592-9. PubMed ID: 17906414
    [Abstract] [Full Text] [Related]

  • 2. Three novel mutations of the PHEX gene in three Chinese families with X-linked dominant hypophosphatemic rickets.
    Xia W, Meng X, Jiang Y, Li M, Xing X, Pang L, Wang O, Pei Y, Yu LY, Sun Y, Hu Y, Zhou X.
    Calcif Tissue Int; 2007 Dec; 81(6):415-20. PubMed ID: 18046499
    [Abstract] [Full Text] [Related]

  • 3. A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia: evidence that the disorder is not a distinct entity from X-linked hypophosphatemic rickets.
    Econs MJ, Friedman NE, Rowe PS, Speer MC, Francis F, Strom TM, Oudet C, Smith JA, Ninomiya JT, Lee BE, Bergen H.
    J Clin Endocrinol Metab; 1998 Oct; 83(10):3459-62. PubMed ID: 9768646
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  • 4. Novel and de novo PHEX mutations in patients with hypophosphatemic rickets.
    Durmaz E, Zou M, Al-Rijjal RA, Baitei EY, Hammami S, Bircan I, Akçurin S, Meyer B, Shi Y.
    Bone; 2013 Jan; 52(1):286-91. PubMed ID: 23079138
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  • 6. Novel PHEX nonsense mutation in a patient with X-linked hypophosphatemic rickets and review of current therapeutic regimens.
    Kienitz T, Ventz M, Kaminsky E, Quinkler M.
    Exp Clin Endocrinol Diabetes; 2011 Jul; 119(7):431-5. PubMed ID: 21553362
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  • 8. X-linked hypophosphatemic rickets associated with respiratory failure.
    Balazs A, Jeha G, Gunn SK, Karaviti LP.
    Clin Pediatr (Phila); 2008 Apr; 47(3):293-5. PubMed ID: 18057152
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  • 9. Regulation of phosphate homeostasis in infants, children, and adolescents, and the role of phosphatonins in this process.
    Garabedian M.
    Curr Opin Pediatr; 2007 Aug; 19(4):488-91. PubMed ID: 17630616
    [Abstract] [Full Text] [Related]

  • 10. A novel Phex mutation in a new mouse model of hypophosphatemic rickets.
    Owen C, Chen F, Flenniken AM, Osborne LR, Ichikawa S, Adamson SL, Rossant J, Aubin JE.
    J Cell Biochem; 2012 Jul; 113(7):2432-41. PubMed ID: 22573557
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  • 11. Novel human pathological mutations. Gene symbol: PHEX. Disease: rickets, hypophosphataemic.
    Ellison J, Tebben P.
    Hum Genet; 2009 Apr; 125(3):339. PubMed ID: 19309785
    [No Abstract] [Full Text] [Related]

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  • 13. X-linked hypophosphatemic rickets and craniosynostosis.
    Murthy AS.
    J Craniofac Surg; 2009 Mar; 20(2):439-42. PubMed ID: 19242361
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  • 14. A clinical and molecular genetic study of hypophosphatemic rickets in children.
    Cho HY, Lee BH, Kang JH, Ha IS, Cheong HI, Choi Y.
    Pediatr Res; 2005 Aug; 58(2):329-33. PubMed ID: 16055933
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  • 15. Identification of two novel mutations in the PHEX gene in Chinese patients with hypophosphatemic rickets/osteomalacia.
    Yue H, Yu JB, He JW, Zhang Z, Fu WZ, Zhang H, Wang C, Hu WW, Gu JM, Hu YQ, Li M, Liu YJ, Zhang ZL.
    PLoS One; 2014 Aug; 9(5):e97830. PubMed ID: 24836714
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  • 16. A novel Phex mutation with defective glycosylation causes hypophosphatemia and rickets in mice.
    Xiong X, Qi X, Ge X, Gu P, Zhao J, Zhao Q, Gao X.
    J Biomed Sci; 2008 Jan; 15(1):47-59. PubMed ID: 17710565
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  • 18. Familial hypophosphatemic rickets caused by a large deletion in PHEX gene.
    Saito T, Nishii Y, Yasuda T, Ito N, Suzuki H, Igarashi T, Fukumoto S, Fujita T.
    Eur J Endocrinol; 2009 Oct; 161(4):647-51. PubMed ID: 19581284
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  • 20. Targeted resequencing of phosphorus metabolism‑related genes in 86 patients with hypophosphatemic rickets/osteomalacia.
    Gu J, Wang C, Zhang H, Yue H, Hu W, He J, Fu W, Zhang Z.
    Int J Mol Med; 2018 Sep; 42(3):1603-1614. PubMed ID: 29901142
    [Abstract] [Full Text] [Related]

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