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Journal Abstract Search

143 related items for PubMed ID: 25553839

  • 1. Novel WISP3 mutations causing spondyloepiphyseal dysplasia tarda with progressive arthropathy in two unrelated Chinese families.
    Liu L, Li N, Zhao Z, Li W, Xia W.
    Joint Bone Spine; 2015 Mar; 82(2):125-8. PubMed ID: 25553839
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  • 2. Novel and recurrent mutations of WISP3 in two Chinese families with progressive pseudorheumatoid dysplasia.
    Sun J, Xia W, He S, Zhao Z, Nie M, Li M, Jiang Y, Xing X, Wang O, Meng X, Zhou X.
    PLoS One; 2012 Mar; 7(6):e38643. PubMed ID: 22685593
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  • 3. Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.
    Dalal A, Bhavani G SL, Togarrati PP, Bierhals T, Nandineni MR, Danda S, Danda D, Shah H, Vijayan S, Gowrishankar K, Phadke SR, Bidchol AM, Rao AP, Nampoothiri S, Kutsche K, Girisha KM.
    Am J Med Genet A; 2012 Nov; 158A(11):2820-8. PubMed ID: 22987568
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  • 4. [Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia].
    Ye J, Zhang HW, Wang T, Cao LF, Qiu WJ, Han LS, Zhang YF, Gu XF.
    Zhonghua Er Ke Za Zhi; 2010 Mar; 48(3):194-8. PubMed ID: 20426955
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  • 5. Mutant WISP3 triggers the phenotype shift of articular chondrocytes by promoting sensitivity to IGF-1 hypothesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy (SEDT-PA).
    Yang Y, Liao E.
    Med Hypotheses; 2007 Mar; 68(6):1406-10. PubMed ID: 17363178
    [Abstract] [Full Text] [Related]

  • 6. A novel compound WISP3 mutation in a Chinese family with progressive pseudorheumatoid dysplasia.
    Luo H, Shi C, Mao C, Jiang C, Bao D, Guo J, Du P, Wang Y, Liu Y, Liu X, Song B, Xu Y.
    Gene; 2015 Jun 10; 564(1):35-8. PubMed ID: 25794430
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  • 7. The diagnostic challenge of progressive pseudorheumatoid dysplasia (PPRD): a review of clinical features, radiographic features, and WISP3 mutations in 63 affected individuals.
    Garcia Segarra N, Mittaz L, Campos-Xavier AB, Bartels CF, Tuysuz B, Alanay Y, Cimaz R, Cormier-Daire V, Di Rocco M, Duba HC, Elcioglu NH, Forzano F, Hospach T, Kilic E, Kuemmerle-Deschner JB, Mortier G, Mrusek S, Nampoothiri S, Obersztyn E, Pauli RM, Selicorni A, Tenconi R, Unger S, Utine GE, Wright M, Zabel B, Warman ML, Superti-Furga A, Bonafé L.
    Am J Med Genet C Semin Med Genet; 2012 Aug 15; 160C(3):217-29. PubMed ID: 22791401
    [Abstract] [Full Text] [Related]

  • 8. Identification of a mutation in the WISP3 gene in three unrelated families with progressive pseudorheumatoid dysplasia.
    Yu Y, Hu M, Xing X, Li F, Song Y, Luo Y, Ma H.
    Mol Med Rep; 2015 Jul 15; 12(1):419-25. PubMed ID: 25738435
    [Abstract] [Full Text] [Related]

  • 9. Patients with progressive pseudorheumatoid dysplasia: from clinical diagnosis to molecular studies.
    Ye J, Zhang HW, Qiu WJ, Han LS, Zhang YF, Gong ZW, Gu XF.
    Mol Med Rep; 2012 Jan 15; 5(1):190-5. PubMed ID: 21993478
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  • 13. Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature.
    Pode-Shakked B, Vivante A, Barel O, Padeh S, Marek-Yagel D, Veber A, Abudi S, Eliyahu A, Tirosh I, Shpilman S, Shril S, Hildebrandt F, Shohat M, Anikster Y.
    BMC Med Genet; 2019 Mar 29; 20(1):53. PubMed ID: 30922245
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  • 16. A homozygous recurring mutation in WISP3 causing progressive pseudorheumatoid arthropathy.
    Temiz F, Ozbek MN, Kotan D, Sangun O, Mungan NO, Yuksel B, Topaloglu AK.
    J Pediatr Endocrinol Metab; 2011 Mar 29; 24(1-2):105-8. PubMed ID: 21528827
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