168 related articles for article (PubMed ID: 22338148)
1. [Analysis of clinical features and gene mutations in 6 patients with Wiskott-Aldrich syndrome].
Jiang MH; Wang ZY; Su J; Cao LJ; Li JQ; Sun XH; Bai X; Wang GF; Ruan CG
Zhonghua Xue Ye Xue Za Zhi; 2011 Sep; 32(9):577-82. PubMed ID: 22338148
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. [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]
5. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Itoh S; Nonoyama S; Morio T; Imai K; Okawa H; Ochs HD; Shimadzu M; Yata J
Int J Hematol; 2000 Jan; 71(1):79-83. PubMed ID: 10729999
[TBL] [Abstract][Full Text] [Related]
6. [Clinical features and genotype analysis of 132 patients with Wiskott-Aldrich syndrome].
Li W; Liu D; Zhang X; Ding Y; Zhao X
Zhonghua Er Ke Za Zhi; 2015 Dec; 53(12):925-30. PubMed ID: 26887548
[TBL] [Abstract][Full Text] [Related]
7. Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome.
Amarinthnukrowh P; Ittiporn S; Tongkobpetch S; Chatchatee P; Sosothikul D; Shotelersuk V; Suphapeetiporn K
Scand J Immunol; 2013 Jan; 77(1):69-74. PubMed ID: 23033889
[TBL] [Abstract][Full Text] [Related]
8. Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.
Gulácsy V; Freiberger T; Shcherbina A; Pac M; Chernyshova L; Avcin T; Kondratenko I; Kostyuchenko L; Prokofjeva T; Pasic S; Bernatowska E; Kutukculer N; Rascon J; Iagaru N; Mazza C; Tóth B; Erdos M; van der Burg M; Maródi L;
Mol Immunol; 2011 Feb; 48(5):788-92. PubMed ID: 21185603
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [The Wiskott-Aldrich syndrome in adulthood].
Matzdorff A; Meindl A; Pralle H
Dtsch Med Wochenschr; 2000 Feb; 125(6):147-50. PubMed ID: 10700878
[TBL] [Abstract][Full Text] [Related]
11. Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome.
Brooimans RA; van den Berg AJ; Tamminga RY; Revesz T; Wulffraat NM; Zegers BJ
Hum Mutat; 2000 Apr; 15(4):386-7. PubMed ID: 10737997
[TBL] [Abstract][Full Text] [Related]
12. Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
Proust A; Guillet B; Picard C; de Saint Basile G; Pondarré C; Tamary H; Dreyfus M; Tchernia G; Fischer A; Delaunay J
Blood Cells Mol Dis; 2007; 39(1):102-6. PubMed ID: 17400488
[TBL] [Abstract][Full Text] [Related]
13. A unique presentation of Wiskott-Aldrich syndrome in relation to platelet size.
Patel PD; Samanich JM; Mitchell WB; Manwani D
Pediatr Blood Cancer; 2011 Jul; 56(7):1127-9. PubMed ID: 21488158
[TBL] [Abstract][Full Text] [Related]
14. CLINICAL FEATURES AND GENETIC ANALYSIS OF SIX PATIENTS WITH WISKOTT-ALDRICH SYNDROME REPORTING TWO NOVEL MUTATIONS: EXPERIENCE OF ERCIYES UNIVERSITY, KAYSERI, TURKEY.
Patiroglu T; Klein C; Gungor HE; Ozdemir MA; Witzel M; Karakukcu M; Sawalle-Belohradsky J; Conca R; Unal E
Genet Couns; 2016; 27(1):9-24. PubMed ID: 27192888
[TBL] [Abstract][Full Text] [Related]
15. Identification of WASP mutations in 10 Australian families with Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Bourne HC; Weston S; Prasad M; Edkins E; Benson EM
Pathology; 2004 Jun; 36(3):262-4. PubMed ID: 15203732
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. A novel large deletion and single nucleotide insertion in the Wiskott-Aldrich syndrome protein gene.
Gulácsy V; Soltész B; Petrescu C; Bataneant M; Gyimesi E; Serban M; Maródi L; Tóth B
Eur J Haematol; 2015 Jul; 95(1):93-8. PubMed ID: 25082437
[TBL] [Abstract][Full Text] [Related]
19. Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation.
Liu DW; Zhang ZY; Zhao Q; Jiang LP; Liu W; Tu WW; Song WX; Zhao XD
Pediatr Blood Cancer; 2015 Sep; 62(9):1601-8. PubMed ID: 25931402
[TBL] [Abstract][Full Text] [Related]
20. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes.
Lemahieu V; Gastier JM; Francke U
Hum Mutat; 1999; 14(1):54-66. PubMed ID: 10447259
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]