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Journal Abstract Search
158 related items for PubMed ID: 29246200
1. 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 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
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 10; 48(3):194-8. PubMed ID: 20426955 [Abstract] [Full Text] [Related]
5. 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 10; 7(6):e38643. PubMed ID: 22685593 [Abstract] [Full Text] [Related]
6. 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 10; 12(1):419-25. PubMed ID: 25738435 [Abstract] [Full Text] [Related]
7. 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 [Abstract] [Full Text] [Related]
8. 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 10; 158A(11):2820-8. PubMed ID: 22987568 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. 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 11; 14(1):16. PubMed ID: 30635069 [Abstract] [Full Text] [Related]
14. 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 11; 5(1):190-5. PubMed ID: 21993478 [Abstract] [Full Text] [Related]
19. 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]
20. 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 15; 85(9):985-96. PubMed ID: 17483925 [Abstract] [Full Text] [Related] Page: [Next] [New Search]