187 related articles for article (PubMed ID: 25476427)
1. [Mutation analysis of WASP gene and prenatal diagnosis of Wiskott-Aldrich syndrome].
Liu N; Shi H; Kong X; Wu Q; Xu X; Bai Q; Feng Y; Zhao Z
Zhonghua Er Ke Za Zhi; 2014 Sep; 52(9):662-6. PubMed ID: 25476427
[TBL] [Abstract][Full Text] [Related]
2. [Analysis of prenatal diagnosis for seven high-risk fetuses with Wiskott-Aldrich syndrome].
Zhao Q; Zhang ZY; Zhao XD; Jiang LP; Zhao Y; Yang XQ
Zhonghua Er Ke Za Zhi; 2012 Jan; 50(1):15-9. PubMed ID: 22456069
[TBL] [Abstract][Full Text] [Related]
3. [Identification of two novel WASP gene mutations in 3 boys with Wiskott-Aldrich syndrome].
Jiang LP; Xu YH; Yang XQ; Liu EM; Wang LJ; Lau YL; Chan KW
Zhonghua Er Ke Za Zhi; 2003 Aug; 41(8):590-3. PubMed ID: 14744380
[TBL] [Abstract][Full Text] [Related]
4. Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families.
Zhang ZY; Xiao HQ; Jiang LP; Zhou Y; Zhao Q; Yu J; Liu W; Yang XQ; Zhao XD
Pediatr Allergy Immunol; 2010 May; 21(3):522-32. PubMed ID: 20546529
[TBL] [Abstract][Full Text] [Related]
5. Molecular characterization of two Malaysian patients with Wiskott-Aldrich syndrome.
Baharin MF; Kader Ibrahim SB; Yap SH; Abdul Manaf AM; Mat Ripen A; Dhaliwal JS
Malays J Pathol; 2015 Aug; 37(2):153-8. PubMed ID: 26277674
[TBL] [Abstract][Full Text] [Related]
6. Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study.
Ferrua F; Cicalese MP; Galimberti S; Giannelli S; Dionisio F; Barzaghi F; Migliavacca M; Bernardo ME; Calbi V; Assanelli AA; Facchini M; Fossati C; Albertazzi E; Scaramuzza S; Brigida I; Scala S; Basso-Ricci L; Pajno R; Casiraghi M; Canarutto D; Salerio FA; Albert MH; Bartoli A; Wolf HM; Fiori R; Silvani P; Gattillo S; Villa A; Biasco L; Dott C; Culme-Seymour EJ; van Rossem K; Atkinson G; Valsecchi MG; Roncarolo MG; Ciceri F; Naldini L; Aiuti A
Lancet Haematol; 2019 May; 6(5):e239-e253. PubMed ID: 30981783
[TBL] [Abstract][Full Text] [Related]
7. Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndrome.
Chan KW; Lee TL; Chung BH; Yang X; Lau YL
Hum Mutat; 2002 Aug; 20(2):151-2. PubMed ID: 12124997
[TBL] [Abstract][Full Text] [Related]
8. Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature.
Eghbali M; Sadeghi-Shabestari M; Najmi Varzaneh F; Zare Bidoki A; Rezaei N
Allergol Immunopathol (Madr); 2016; 44(5):450-4. PubMed ID: 26993433
[TBL] [Abstract][Full Text] [Related]
9. Molecular diagnosis of Wiskott-Aldrich syndrome in Taiwan.
Chien YH; Hwu WL; Ariga T; Chang KW; Yang YH; Lin KH; Chiang BL
J Microbiol Immunol Infect; 2004 Oct; 37(5):276-81. PubMed ID: 15497008
[TBL] [Abstract][Full Text] [Related]
10. Detection of six novel mutations in WASP gene in fifteen Iranian Wiskott-Aldrich patients.
Safaei S; Fazlollahi MR; Houshmand M; Hamidieh AA; Bemanian MH; Alavi S; Mousavi F; Pourpak Z; Moin M
Iran J Allergy Asthma Immunol; 2012 Dec; 11(4):345-8. PubMed ID: 23264413
[TBL] [Abstract][Full Text] [Related]
11. Clinical aspects and genetic analysis of taiwanese patients with wiskott-Aldrich syndrome protein mutation: the first identification of x-linked thrombocytopenia in the chinese with novel mutations.
Lee WI; Huang JL; Jaing TH; Wu KH; Chien YH; Chang KW
J Clin Immunol; 2010 Jul; 30(4):593-601. PubMed ID: 20232122
[TBL] [Abstract][Full Text] [Related]
12. The genotype of the original Wiskott phenotype.
Binder V; Albert MH; Kabus M; Bertone M; Meindl A; Belohradsky BH
N Engl J Med; 2006 Oct; 355(17):1790-3. PubMed ID: 17065640
[TBL] [Abstract][Full Text] [Related]
13. Identification of a novel WAS mutation and the non-splicing effect of a second-site mutation in a Chinese pedigree with Wiskott-Aldrich syndrome.
Ji X; Hou X; Guo X; Sun Y; Ma F; Hao J
Orphanet J Rare Dis; 2022 Dec; 17(1):447. PubMed ID: 36550574
[TBL] [Abstract][Full Text] [Related]
14. When
Jin YY; Wu J; Chen TX; Chen J
Front Immunol; 2019; 10():1549. PubMed ID: 31354712
[No Abstract] [Full Text] [Related]
15. Wiskott-Aldrich syndrome in a girl caused by heterozygous WASP mutation and extremely skewed X-chromosome inactivation: a novel association with maternal uniparental isodisomy 6.
Takimoto T; Takada H; Ishimura M; Kirino M; Hata K; Ohara O; Morio T; Hara T
Neonatology; 2015; 107(3):185-90. PubMed ID: 25633059
[TBL] [Abstract][Full Text] [Related]
16. Wiskott-Aldrich Syndrome in four male siblings from a consanguineous family from Lebanon.
Mansour R; El-Orfali Y; Saber A; Noun D; Youssef N; Youssef Y; Hanna-Wakim R; Dbaibo G; Abboud M; Massaad MJ
Clin Immunol; 2020 Oct; 219():108573. PubMed ID: 32814211
[TBL] [Abstract][Full Text] [Related]
17. Two novel mutations identified in the Wiskott-Aldrich syndrome protein gene cause Wiskott-Aldrich syndrome and thrombocytopenia.
Andreu N; Matamoros N; Escudero A; Fillat C
Int J Mol Med; 2007 May; 19(5):777-82. PubMed ID: 17390083
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndrome.
Kim HJ; Yoo EH; Ki CS; Yoo GH; Koo HH; Kim JW; Kim SH
Int J Hematol; 2006 Jun; 83(5):426-8. PubMed ID: 16787874
[TBL] [Abstract][Full Text] [Related]
19. Clinical aspects and molecular analysis of Chinese patients with Wiskott-Aldrich syndrome in Taiwan.
Lee WI; Yang CY; Jaing TH; Huang JL; Chien YH; Chang KW
Int Arch Allergy Immunol; 2008; 145(1):15-23. PubMed ID: 17703096
[TBL] [Abstract][Full Text] [Related]
20. Clinical and molecular characteristics of Wiskott-Aldrich Syndrome in five unrelated Chinese families.
Jiang J; Zhou J; Wei M; Singh S; Nikuze L; Huang L; Li Y; Jiang J; Wei H
Scand J Immunol; 2022 Jan; 95(1):e13115. PubMed ID: 34758123
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
