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Journal Abstract Search


166 related items for PubMed ID: 16152649

  • 21. Clinical and molecular characterization in a cohort of patients with progressive pseudorheumatoid dysplasia.
    El Dessouki D, Amr K, Kholoussi N, Rady HM, Temtamy SA, Abdou MMS, Aglan M.
    Am J Med Genet A; 2023 Sep; 191(9):2329-2336. PubMed ID: 37377052
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  • 22. 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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  • 24. 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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  • 26. Progressive pseudorheumatoid dysplasia misdiagnosed as juvenile idiopathic arthritis: a case report.
    Omar AA, Ahmed S, Rodrigues JC, Kayiza A, Owino L.
    J Med Case Rep; 2021 Nov 08; 15(1):551. PubMed ID: 34749805
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  • 27. Progressive pseudorheumatoid chondrodysplasia: a report of nine cases in three families.
    Rezai-Delui H, Mamoori G, Sadri-Mahvelati E, Noori NM.
    Skeletal Radiol; 1994 Aug 08; 23(6):411-9. PubMed ID: 7992106
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  • 29. A Rare Skeletal Dysplasia-Close Mimicker Of Juvenile Idiopathic Arthritis-Progressive Pseudorheumatoid Dysplasia.
    Riaz M, Khoso Z, Rai VR, Hanif MI, Ibrahim MN, Raza SJ.
    J Ayub Med Coll Abbottabad; 2022 Aug 08; 34(Suppl 1)(4):S1050-S1052. PubMed ID: 36550675
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  • 30. Progressive pseudorheumatoid dysplasia with new-found gene mutation of Wntl inducible signaling pathway protein 3.
    Chen W, Mo S, Luo G, Wang Y, Deng X, Zhu J, Zhao W.
    Pediatr Rheumatol Online J; 2018 Sep 10; 16(1):55. PubMed ID: 30200995
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  • 35. 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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  • 38. A homozygous deletion of exon 1 in WISP3 causes progressive pseudorheumatoid dysplasia in two siblings.
    Neerinckx B, Thues C, Wouters C, Lechner S, Westhovens R, Van Esch H.
    Hum Genome Var; 2015 Sep 07; 2():15049. PubMed ID: 27081554
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