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Journal Abstract Search

202 related items for PubMed ID: 26991965

  • 1. Early severe scoliosis in a patient with atypical progressive pseudorheumatoid dysplasia (PPD): Identification of two WISP3 mutations, one previously unreported.
    Montané LS, Marín OR, Rivera-Pedroza CI, Vallespín E, Del Pozo Á, Heath KE.
    Am J Med Genet A; 2016 Jun; 170(6):1595-9. PubMed ID: 26991965
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  • 2. Delayed-onset of progressive pseudorheumatoid dysplasia in a Chinese adult with a novel compound WISP3 mutation: a case report.
    Hu Q, Liu J, Wang Y, Wang J, Shi H, Sun Y, Wu X, Yang C, Teng J.
    BMC Med Genet; 2017 Dec 15; 18(1):149. PubMed ID: 29246200
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  • 6. WISP3 mutation associated with pseudorheumatoid dysplasia.
    Sailani MR, Chappell J, Jingga I, Narasimha A, Zia A, Lynch JL, Mazrouei S, Bernstein JA, Aryani O, Snyder MP.
    Cold Spring Harb Mol Case Stud; 2018 Feb 15; 4(1):. PubMed ID: 29092958
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  • 9. Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India.
    Rai E, Mahajan A, Kumar P, Angural A, Dhar MK, Razdan S, Thangaraj K, Wise CA, Ikegawa S, Pandita KK, Sharma S.
    Sci Rep; 2016 Jun 13; 6():27684. PubMed ID: 27291587
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  • 10. 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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  • 11. 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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  • 14. Progressive pseudorheumatoid dysplasia: a rare childhood disease.
    Torreggiani S, Torcoletti M, Campos-Xavier B, Baldo F, Agostoni C, Superti-Furga A, Filocamo G.
    Rheumatol Int; 2019 Mar 10; 39(3):441-452. PubMed ID: 30327864
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  • 15. Identification of novel mutations in WISP3 gene in two unrelated Chinese families with progressive pseudorheumatoid dysplasia.
    Yue H, Zhang ZL, He JW.
    Bone; 2009 Apr 10; 44(4):547-54. PubMed ID: 19064006
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  • 16. Coexistence of a novel WISP3 pathogenic variant and an MEFV mutation in an Arabic family with progressive pseudorheumatoid dysplasia mimicking polyarticular juvenile idiopathic arthritis.
    Fathalla BM, Elgabaly EA, Tayoun AA.
    Pediatr Rheumatol Online J; 2020 Sep 07; 18(1):69. PubMed ID: 32894151
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  • 18. 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 07; 5(1):190-5. PubMed ID: 21993478
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  • 19. 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 07; 82(2):125-8. PubMed ID: 25553839
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  • 20. Molecular study of WISP3 in nine families originating from the Middle-East and presenting with progressive pseudorheumatoid dysplasia: identification of two novel mutations, and description of a founder effect.
    Delague V, Chouery E, Corbani S, Ghanem I, Aamar S, Fischer J, Levy-Lahad E, Urtizberea JA, Mégarbané A.
    Am J Med Genet A; 2005 Oct 01; 138A(2):118-26. PubMed ID: 16152649
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