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Journal Abstract Search

285 related items for PubMed ID: 24229582

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  • 3. Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets.
    Li SS, Gu JM, Yu WJ, He JW, Fu WZ, Zhang ZL.
    Int J Mol Med; 2016 Dec; 38(6):1703-1714. PubMed ID: 27840894
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  • 5. [Novel PHEX gene mutations in patients with X-linked hypophosphatemic rickets: an analysis of 2 cases].
    Ran Q, Xiong F, Zhu M, Deng LL, Lei PY, Luo YH, Zeng Y, Zhu GH, Song C.
    Zhongguo Dang Dai Er Ke Za Zhi; 2017 May; 19(5):534-538. PubMed ID: 28506344
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  • 7. 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
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  • 8. PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets.
    Song HR, Park JW, Cho DY, Yang JH, Yoon HR, Jung SC.
    J Korean Med Sci; 2007 Dec; 22(6):981-6. PubMed ID: 18162710
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  • 9. 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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  • 10. Clinical and genetic analysis in a large Chinese cohort of patients with X-linked hypophosphatemia.
    Zhang C, Zhao Z, Sun Y, Xu L, JiaJue R, Cui L, Pang Q, Jiang Y, Li M, Wang O, He X, He S, Nie M, Xing X, Meng X, Zhou X, Yan L, Kaplan JM, Insogna KL, Xia W.
    Bone; 2019 Apr; 121():212-220. PubMed ID: 30682568
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  • 11. Mutational survey of the PHEX gene in patients with X-linked hypophosphatemic rickets.
    Ichikawa S, Traxler EA, Estwick SA, Curry LR, Johnson ML, Sorenson AH, Imel EA, Econs MJ.
    Bone; 2008 Oct; 43(4):663-6. PubMed ID: 18625346
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  • 14. Functional analysis of 22 splice-site mutations in the PHEX, the causative gene in X-linked dominant hypophosphatemic rickets.
    BinEssa HA, Zou M, Al-Enezi AF, Alomrani B, Al-Faham MSA, Al-Rijjal RA, Meyer BF, Shi Y.
    Bone; 2019 Aug; 125():186-193. PubMed ID: 31102713
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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 mosaic mutation of phosphate-regulating gene with homologies to endopeptidases on the X chromosome (PHEX) in X-linked hypophosphatemic rickets with mild bone phenotypes.
    Asano S, Sako S, Funasaki Y, Takeshita Y, Niida Y, Takamura T.
    Endocr J; 2021 Sep 28; 68(9):1135-1141. PubMed ID: 33907069
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  • 17. Normal growth and muscle dysfunction in X-linked hypophosphatemic rickets associated with a novel mutation in the PHEX gene.
    Makras P, Hamdy NA, Kant SG, Papapoulos SE.
    J Clin Endocrinol Metab; 2008 Apr 28; 93(4):1386-9. PubMed ID: 18252791
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  • 18. Novel PHEX gene mutation associated with X linked hypophosphatemic rickets.
    Chandran M, Chng CL, Zhao Y, Bee YM, Phua LY, Clarke BL.
    Nephron Physiol; 2010 Apr 28; 116(3):p17-21. PubMed ID: 20664300
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  • 19. Prenatal diagnosis for a novel splice mutation of PHEX gene in a large Han Chinese family affected with X-linked hypophosphatemic rickets.
    Qiu G, Liu C, Zhou J, Liu P, Wang J, Jiang H, Hou Z, Zhao Y, Sun K, Li-Ling J.
    Genet Test Mol Biomarkers; 2010 Jun 28; 14(3):385-91. PubMed ID: 20578943
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