151 related articles for article (PubMed ID: 34397000)
1. Wiskott-Aldrich syndrome with possible congenital
Sobouti B; Bahrami A; Rahmani F; Talebi S; Sherafati V; Vafapour M; Rezaei N
Natl Med J India; 2021; 34(1):24-26. PubMed ID: 34397000
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report.
Baharin MF; Dhaliwal JS; Sarachandran SV; Idris SZ; Yeoh SL
J Med Case Rep; 2016 Jun; 10(1):188. PubMed ID: 27356510
[TBL] [Abstract][Full Text] [Related]
9. [Wiskott-Aldrich syndrome].
Gulácsy V; Maródi L
Orv Hetil; 2008 Jul; 149(29):1367-71. PubMed ID: 18617469
[TBL] [Abstract][Full Text] [Related]
10. Clinical, Laboratory Features and Clinical Courses of Patients with Wiskott Aldrich Syndrome and X-linked Thrombocytopenia-A single center study.
Bildik HN; Cagdas D; Ozturk Kura A; Oskay Halacli S; Sanal O; Tezcan I
Immunol Invest; 2022 Jul; 51(5):1272-1283. PubMed ID: 34098853
[TBL] [Abstract][Full Text] [Related]
11. A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection.
Kaya Z; Muluk C; Hakoloğlu Ş; Tufan LŞ
Turk J Haematol; 2019 Feb; 36(1):70-71. PubMed ID: 29983408
[No Abstract] [Full Text] [Related]
12. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. [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]
19. 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]
20. 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]
[Next] [New Search]
