161 related articles for article (PubMed ID: 16787874)
1. 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]
2. 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]
3. A novel WASP gene mutation in a Chinese boy with Wiskott-Aldrich syndrome.
Yu H; Liu T; Meng W; Hou L
Int J Hematol; 2010 Sep; 92(2):271-5. PubMed ID: 20683686
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [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]
7. A novel termination codon mutation of the WAS gene in a Thai family with Wiskott-Aldrich syndrome.
Chatchatee P; Srichomthong C; Chewatavorn A; Shotelersuk V
Int J Mol Med; 2003 Dec; 12(6):939-41. PubMed ID: 14612970
[TBL] [Abstract][Full Text] [Related]
8. A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.
Doğu F; Ariga T; Ikincioğullari A; Bozdoğan G; Aytekin C; Metin A; Babacan E
Turk J Pediatr; 2006; 48(1):66-8. PubMed ID: 16562789
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Clinical and genetic analysis of 2 rare cases of Wiskott-Aldrich syndrome from Chinese minorities: Two case reports.
Liu H; Wang Y; Li Y; Tao L; Zhang Y; He X; Zhou Y; Liu X; Wang Y; Li L
Medicine (Baltimore); 2021 Apr; 100(16):e25527. PubMed ID: 33879693
[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. [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]
13. IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family.
Yoon SH; Cho T; Kim HJ; Kim SY; Ko JH; Baek HS; Lee HJ; Lee CH
Pediatr Blood Cancer; 2012 Feb; 58(2):297-9. PubMed ID: 22038941
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Recurrent V75M mutation within the Wiskott-Aldrich syndrome protein: description of a homozygous female patient.
Proust A; Guillet B; Pellier I; Rachieru P; Hoarau C; Claeyssens S; Léonard C; Charrier S; Vainchenker W; Tchernia G; Delaunay J
Eur J Haematol; 2005 Jul; 75(1):54-9. PubMed ID: 15946311
[TBL] [Abstract][Full Text] [Related]
16. A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.
Park SK; Kim CS; Song DK; Kim JY; Choi IJ; Kim DK
J Korean Med Sci; 2007 Dec; 22(6):998-1001. PubMed ID: 18162713
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Wiskott-Aldrich syndrome with macrothrombocytopenia.
Skoric D; Dimitrijevic A; Cuturilo G; Ivanovski P
Indian Pediatr; 2014 Dec; 51(12):1015-6. PubMed ID: 25560165
[TBL] [Abstract][Full Text] [Related]
19. Wiskott-Aldrich syndrome: Two case reports with a novel mutation.
Kamuran K; Çetin M; Geylan H; Karaman S; Demir N; Yurekturk E; Yavuz İ; Yavuz G; Tuncer O
Pediatr Hematol Oncol; 2017 Aug; 34(5):286-291. PubMed ID: 29200320
[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]