124 related articles for article (PubMed ID: 34650595)
1. Case Report: Recurrent Variant c.298 TA in
Sheth H; Shah J; Nair A; Naik P; Sheth J
Front Genet; 2021; 12():724824. PubMed ID: 34650595
[TBL] [Abstract][Full Text] [Related]
2. A Novel Homozygous Frameshift Mutation in
Gaboon NEA; Parveen A; El Beheiry A; Al-Aama JY; Alsaedi MS; Wasif N
Front Pediatr; 2019; 7():245. PubMed ID: 31294002
[No Abstract] [Full Text] [Related]
3. 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]
4. Progressive Pseudorheumatoid Dysplasia of Childhood (PPRD)-A Case Series with Recurrent c.740_741del Variant.
Nilay M; Rawool A; Mandal K
J Pediatr Genet; 2024 Mar; 13(1):62-68. PubMed ID: 38567170
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. WISP3 mutational analysis in Indian patients diagnosed with progressive pseudorheumatoid dysplasia and report of a novel mutation at p.Y198.
Madhuri V; Santhanam M; Rajagopal K; Sugumar LK; Balaji V
Bone Joint Res; 2016 Jul; 5(7):301-6. PubMed ID: 27436824
[TBL] [Abstract][Full Text] [Related]
7. CCN6 mutation detection in Chinese patients with progressive pseudo-rheumatoid dysplasia and identification of four novel mutations.
Wang Y; Xiao K; Yang Y; Wu Z; Jin J; Qiu G; Weng X; Zhao X
Mol Genet Genomic Med; 2020 Jul; 8(7):e1261. PubMed ID: 32351055
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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]
10. Specific early signs and long-term follow-up findings of progressive pseudorheumatoid dysplasia (PPRD) in the Turkish cohort.
Uludağ Alkaya D; Kasapçopur Ö; Bursalı A; Adrovic A; Demir B; Aykut A; Tüysüz B
Rheumatology (Oxford); 2022 Aug; 61(9):3693-3703. PubMed ID: 34919662
[TBL] [Abstract][Full Text] [Related]
11. 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; 15(1):551. PubMed ID: 34749805
[TBL] [Abstract][Full Text] [Related]
12. Unique mutation spectrum of progressive pseudorheumatoid dysplasia in the Chinese population: a retrospective genotype-phenotype analysis of 105 patients.
Wang W; Gao SH; Wei M; Zhong LQ; Liu W; Jian S; Xiao J; Zhang CH; Zhang JG; Zeng XF; Xia WB; Qiu ZQ; Song HM
World J Pediatr; 2023 Jul; 19(7):674-686. PubMed ID: 36622578
[TBL] [Abstract][Full Text] [Related]
13. A retrospective study of nine patients with progressive pseudorheumatoid dysplasia: to explore early diagnosis and further treatment.
Yin L; Mao Y; Zhou Y; Shen Y; Chen H; Zhou W; Jin Y; Huang H; Yu Y; Wang J
Clin Rheumatol; 2022 Mar; 41(3):877-888. PubMed ID: 34674084
[TBL] [Abstract][Full Text] [Related]
14. 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]
15.
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]
16. 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; 6():27684. PubMed ID: 27291587
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Novel COL2A1 variant (c.619G>A, p.Gly207Arg) manifesting as a phenotype similar to progressive pseudorheumatoid dysplasia and spondyloepiphyseal dysplasia, Stanescu type.
Jurgens J; Sobreira N; Modaff P; Reiser CA; Seo SH; Seong MW; Park SS; Kim OH; Cho TJ; Pauli RM
Hum Mutat; 2015 Oct; 36(10):1004-8. PubMed ID: 26183434
[TBL] [Abstract][Full Text] [Related]
19. 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; 2():15049. PubMed ID: 27081554
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]