170 related articles for article (PubMed ID: 37052865)
1. A Novel Mutation Leading to Wiskott-Aldrich Syndrome in an Ethiopian Boy: a Case Report and a Review of Literature.
Alemayehu T; Vinh DC
J Clin Immunol; 2023 Aug; 43(6):1272-1277. PubMed ID: 37052865
[TBL] [Abstract][Full Text] [Related]
2. A Clinical Diagnosis of Wiskott Aldrich Syndrome in an Ethiopian Boy with Recurrent Sinopulmonary Infections: A Case Report.
Deribssa SJ; Alemayehu T
Ethiop J Health Sci; 2020 Nov; 30(6):1051-1054. PubMed ID: 33883853
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Identification of a novel WAS mutation in a South African patient presenting with atypical Wiskott-Aldrich syndrome: a case report.
Glanzmann B; Möller M; Schoeman M; Urban M; van Helden PD; Frigati L; Grewal R; Pieters H; Loos B; Hoal EG; Glashoff RH; Cornelissen H; Rabie H; Esser MM; Kinnear CJ
BMC Med Genet; 2020 Jun; 21(1):124. PubMed ID: 32503528
[TBL] [Abstract][Full Text] [Related]
5. [Wiskott-Aldrich syndrome with platelets of normal size and c.295C>T mutation of the WAS gene. Case report].
Cunha-Carneiro ML; Xavier-Andrade M; Bacarini-Leite LF; Mosca T; Carvalho Neves Forte W
Rev Alerg Mex; 2023 Apr; 69(4):228-231. PubMed ID: 37218050
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. Confirmed diagnosis of classic Wiskott-Aldrich syndrome in East Africa: a case report.
Kiputa M; Urio O; Maghembe A; Kombo D; Dhalla S; Ndembo V; Muze K; Kahwa M; Fakih Z; Kija E
J Med Case Rep; 2022 Jul; 16(1):301. PubMed ID: 35897083
[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. 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]
12. Report of clinical presentations and two novel mutations in patients with Wiskott-Aldrich syndrome/X-linked Thrombocytopenia.
Udomkittivorakul N; Wattanasirichaigoon D; Manuyakorn W; Pongphitcha P; Khongkraparn A; Tunlayadechanont P; Sirachainan N
Platelets; 2022 Jul; 33(5):792-796. PubMed ID: 34705590
[TBL] [Abstract][Full Text] [Related]
13. [Wiskott-Aldrich syndrome].
Gulácsy V; Maródi L
Orv Hetil; 2008 Jul; 149(29):1367-71. PubMed ID: 18617469
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A novel mutation in Wiskott-Aldrich gene manifesting as macrothrombocytopenia and neutropenia.
Arwani M; Lee D; Haddad A; Mewawalla P
BMJ Case Rep; 2018 Jul; 2018():. PubMed ID: 29991546
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
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. [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]
20. A novel splice site mutation in WAS gene in patient with Wiskott-Aldrich syndrome and chronic colitis: a case report.
Esmaeilzadeh H; Bordbar MR; Dastsooz H; Silawi M; Fard MAF; Adib A; Kafashan A; Tabatabaei Z; Sadeghipour F; Faghihi MA
BMC Med Genet; 2018 Jul; 19(1):123. PubMed ID: 30029636
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
