154 related articles for article (PubMed ID: 22685593)
1. 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; 7(6):e38643. PubMed ID: 22685593
[TBL] [Abstract][Full Text] [Related]
2. 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; 564(1):35-8. PubMed ID: 25794430
[TBL] [Abstract][Full Text] [Related]
3. 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; 12(1):419-25. PubMed ID: 25738435
[TBL] [Abstract][Full Text] [Related]
4. 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
[TBL] [Abstract][Full Text] [Related]
5. [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
[TBL] [Abstract][Full Text] [Related]
6. 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; 5(1):190-5. PubMed ID: 21993478
[TBL] [Abstract][Full Text] [Related]
7. 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
[TBL] [Abstract][Full Text] [Related]
8. 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; 44(4):547-54. PubMed ID: 19064006
[TBL] [Abstract][Full Text] [Related]
9. 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; 160C(3):217-29. PubMed ID: 22791401
[TBL] [Abstract][Full Text] [Related]
10. 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; 24(1-2):105-8. PubMed ID: 21528827
[TBL] [Abstract][Full Text] [Related]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. 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; 18(1):149. PubMed ID: 29246200
[TBL] [Abstract][Full Text] [Related]
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; 20(1):53. PubMed ID: 30922245
[TBL] [Abstract][Full Text] [Related]
14. Progressive pseudorheumatoid dysplasia confirmed by whole-exon sequencing in a Chinese adult before corrective surgery.
Li Y; Zeng Y; Chen Z; Xin H; Li X
J Orthop Surg Res; 2019 Jan; 14(1):16. PubMed ID: 30635069
[TBL] [Abstract][Full Text] [Related]
15. Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation.
Zhou HD; Bu YH; Peng YQ; Xie H; Wang M; Yuan LQ; Jiang Y; Li D; Wei QY; He YL; Xiao T; Ni JD; Liao EY
J Mol Med (Berl); 2007 Sep; 85(9):985-96. PubMed ID: 17483925
[TBL] [Abstract][Full Text] [Related]
16.
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; 4(1):. PubMed ID: 29092958
[TBL] [Abstract][Full Text] [Related]
17. 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; 16(1):55. PubMed ID: 30200995
[TBL] [Abstract][Full Text] [Related]
18. 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; 138A(2):118-26. PubMed ID: 16152649
[TBL] [Abstract][Full Text] [Related]
19. 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; 39(3):441-452. PubMed ID: 30327864
[TBL] [Abstract][Full Text] [Related]
20. 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
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]