168 related articles for article (PubMed ID: 22338148)
21. Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome.
Boztug K; Germeshausen M; Avedillo Díez I; Gulacsy V; Diestelhorst J; Ballmaier M; Welte K; Maródi L; Chernyshova L; Klein C
Clin Genet; 2008 Jul; 74(1):68-74. PubMed ID: 18479478
[TBL] [Abstract][Full Text] [Related]
22. Wiskott-Aldrich syndrome in Argentina: 17 unique, including nine novel, mutations.
El-Hakeh J; Rosenzweig S; Oleastro M; Basack N; Berozdnik L; Molina F; Rivas EM; Zelazko M; Danielian S
Hum Mutat; 2002 Feb; 19(2):186-7. PubMed ID: 11793485
[TBL] [Abstract][Full Text] [Related]
23. Wiskott-Aldrich syndrome is an important differential diagnosis in male infants with juvenile myelomonocytic leukemialike features.
Watanabe N; Yoshimi A; Kamachi Y; Kawabe T; Muramatsu H; Matsumoto K; Manabe A; Kojima S; Kato K
J Pediatr Hematol Oncol; 2007 Dec; 29(12):836-8. PubMed ID: 18090932
[TBL] [Abstract][Full Text] [Related]
24. When
Jin YY; Wu J; Chen TX; Chen J
Front Immunol; 2019; 10():1549. PubMed ID: 31354712
[No Abstract] [Full Text] [Related]
25. 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]
26. 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]
27. [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]
28. Wiskott-Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia.
Yoshimi A; Kamachi Y; Imai K; Watanabe N; Nakadate H; Kanazawa T; Ozono S; Kobayashi R; Yoshida M; Kobayashi C; Hama A; Muramatsu H; Sasahara Y; Jakob M; Morio T; Ehl S; Manabe A; Niemeyer C; Kojima S
Pediatr Blood Cancer; 2013 May; 60(5):836-41. PubMed ID: 23023736
[TBL] [Abstract][Full Text] [Related]
29. Wiskott-Aldrich syndrome.
Notarangelo LD; Miao CH; Ochs HD
Curr Opin Hematol; 2008 Jan; 15(1):30-6. PubMed ID: 18043243
[TBL] [Abstract][Full Text] [Related]
30. Wiskott-Aldrich syndrome complicated by an atypical lymphoproliferative disorder: a case report.
Ma YC; Shyur SD; Ho TY; Huang LH; Wu JY; Liang DC; Chien YH
J Microbiol Immunol Infect; 2005 Aug; 38(4):289-92. PubMed ID: 16118678
[TBL] [Abstract][Full Text] [Related]
31. Microthrombocytopenia in a male infant with cytomegalovirus.
Krishnan KR; Vega R
Ann Allergy Asthma Immunol; 2009 Sep; 103(3):268-9. PubMed ID: 19788027
[No Abstract] [Full Text] [Related]
32. 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]
33. Molecular biology of the Wiskott-Aldrich syndrome.
Rengan R; Ochs HD
Rev Immunogenet; 2000; 2(2):243-55. PubMed ID: 11258421
[TBL] [Abstract][Full Text] [Related]
34. Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features.
Ariga T
Allergol Int; 2012 Jun; 61(2):183-9. PubMed ID: 22361515
[TBL] [Abstract][Full Text] [Related]
35. The Wiskott-Aldrich syndrome.
Ochs HD
Semin Hematol; 1998 Oct; 35(4):332-45. PubMed ID: 9801262
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Characterization of a deletion mutation involving exons 3-7 of the WASP gene detected in a patient with Wiskott-Aldrich syndrome.
Ariga T; Yamada M; Ito S; Iwamura M; Iseki M; Sakiyama Y
Hum Mutat; 1997; 10(4):310-6. PubMed ID: 9338585
[TBL] [Abstract][Full Text] [Related]
39. Mutations that cause the Wiskott-Aldrich syndrome impair the interaction of Wiskott-Aldrich syndrome protein (WASP) with WASP interacting protein.
Stewart DM; Tian L; Nelson DL
J Immunol; 1999 Apr; 162(8):5019-24. PubMed ID: 10202051
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
