170 related articles for article (PubMed ID: 15218418)
1. Confirming or excluding the diagnosis of Wiskott-Aldrich syndrome in children with thrombocytopenia of an unknown etiology.
Ariga T; Nakajima M; Yoshida J; Yamato K; Nagatoshi Y; Yanai F; Caviles AP; Nelson DL; Sakiyama Y
J Pediatr Hematol Oncol; 2004 Jul; 26(7):435-40. PubMed ID: 15218418
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus.
Kolluri R; Shehabeldin A; Peacocke M; Lamhonwah AM; Teichert-Kuliszewska K; Weissman SM; Siminovitch KA
Hum Mol Genet; 1995 Jul; 4(7):1119-26. PubMed ID: 8528198
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.
Derry JM; Kerns JA; Weinberg KI; Ochs HD; Volpini V; Estivill X; Walker AP; Francke U
Hum Mol Genet; 1995 Jul; 4(7):1127-35. PubMed ID: 8528199
[TBL] [Abstract][Full Text] [Related]
8. Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein.
Medina SS; Siqueira LH; Colella MP; Yamaguti-Hayakawa GG; Duarte BKL; Dos Santos Vilela MM; Ozelo MC
BMC Pediatr; 2017 Jun; 17(1):151. PubMed ID: 28641574
[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. Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations.
Kawai S; Minegishi M; Ohashi Y; Sasahara Y; Kumaki S; Konno T; Miki H; Derry J; Nonoyama S; Miyawaki T; Horibe K; Tachibana N; Kudoh E; Yoshimura Y; Izumikawa Y; Sako M; Tsuchiya S
J Immunol Methods; 2002 Feb; 260(1-2):195-205. PubMed ID: 11792389
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
14. Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients.
MacCarthy-Morrogh L; Gaspar HB; Wang YC; Katz F; Thompson L; Layton M; Jones AM; Kinnon C
Clin Immunol Immunopathol; 1998 Jul; 88(1):22-7. PubMed ID: 9683546
[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. Childhood-onset inflammatory bowel diseases associated with mutation of Wiskott-Aldrich syndrome protein gene.
Ohya T; Yanagimachi M; Iwasawa K; Umetsu S; Sogo T; Inui A; Fujisawa T; Ito S
World J Gastroenterol; 2017 Dec; 23(48):8544-8552. PubMed ID: 29358862
[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. 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]
19. [Analysis of prenatal diagnosis for seven high-risk fetuses with Wiskott-Aldrich syndrome].
Zhao Q; Zhang ZY; Zhao XD; Jiang LP; Zhao Y; Yang XQ
Zhonghua Er Ke Za Zhi; 2012 Jan; 50(1):15-9. PubMed ID: 22456069
[TBL] [Abstract][Full Text] [Related]
20. The Wiskott-Aldrich syndrome.
Ochs HD
Springer Semin Immunopathol; 1998; 19(4):435-58. PubMed ID: 9618767
[No Abstract] [Full Text] [Related]
[Next] [New Search]