158 related articles for article (PubMed ID: 37218050)
21. Wiskott-Aldrich syndrome protein and platelets.
Oda A; Ochs HD
Immunol Rev; 2000 Dec; 178():111-7. PubMed ID: 11213795
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. Current and emerging treatment options for Wiskott-Aldrich syndrome.
Worth AJ; Thrasher AJ
Expert Rev Clin Immunol; 2015; 11(9):1015-32. PubMed ID: 26159751
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome.
Candotti F
J Clin Immunol; 2018 Jan; 38(1):13-27. PubMed ID: 29086100
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. When
Jin YY; Wu J; Chen TX; Chen J
Front Immunol; 2019; 10():1549. PubMed ID: 31354712
[No Abstract] [Full Text] [Related]
30. 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]
31. Protein assays for diagnosis of Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Qasim W; Gilmour KC; Heath S; Ashton E; Cranston T; Thomas A; Finn A; Davies EG; Thrasher AJ; Kinnon C; Jones A; Gaspar HB
Br J Haematol; 2001 Jun; 113(4):861-5. PubMed ID: 11442475
[TBL] [Abstract][Full Text] [Related]
32. [Congenital thrombocytopenia in adults].
van Zweeden A; Bot P; Smets Y; Terpstra W
Ned Tijdschr Geneeskd; 2011; 155():A2634. PubMed ID: 21382213
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. 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]
36. Clinical aspects and molecular analysis of Chinese patients with Wiskott-Aldrich syndrome in Taiwan.
Lee WI; Yang CY; Jaing TH; Huang JL; Chien YH; Chang KW
Int Arch Allergy Immunol; 2008; 145(1):15-23. PubMed ID: 17703096
[TBL] [Abstract][Full Text] [Related]
37. Successful renal transplantation in a patient with a Wiskott-Aldrich syndrome protein (WASP) gene mutation.
Chovancova Z; Kuman M; Vlkova M; Litzman J
Transpl Int; 2015 Aug; 28(8):1005-9. PubMed ID: 25864580
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. A multiinstitutional survey of the Wiskott-Aldrich syndrome.
Sullivan KE; Mullen CA; Blaese RM; Winkelstein JA
J Pediatr; 1994 Dec; 125(6 Pt 1):876-85. PubMed ID: 7996359
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]