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Items: 1 to 20 of 146

1.

Wiskott-Aldrich syndrome is an important differential diagnosis in male infants with juvenile myelomonocytic leukemialike features.

Watanabe N, Yoshimi A, Kamachi Y, Kawabe T, Muramatsu H, Matsumoto K, Manabe A, Kojima S, Kato K.

J Pediatr Hematol Oncol. 2007 Dec;29(12):836-8.

PMID:
18090932
2.

Wiskott-Aldrich syndrome with unusual clinical features similar to juvenile myelomonocytic leukemia.

Sano H, Kobayashi R, Suzuki D, Yasuda K, Nakanishi M, Nagashima T, Yamada M, Kobayashi K.

Int J Hematol. 2012 Aug;96(2):279-83. doi: 10.1007/s12185-012-1130-x. Epub 2012 Jun 27.

PMID:
22736231
3.

Wiskott-Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia.

Yoshimi A, Kamachi Y, Imai K, Watanabe N, Nakadate H, Kanazawa T, Ozono S, Kobayashi R, Yoshida M, Kobayashi C, Hama A, Muramatsu H, Sasahara Y, Jakob M, Morio T, Ehl S, Manabe A, Niemeyer C, Kojima S.

Pediatr Blood Cancer. 2013 May;60(5):836-41. doi: 10.1002/pbc.24359. Epub 2012 Sep 28.

PMID:
23023736
4.

Wiskott-Aldrich syndrome; an x-linked primary immunodeficiency disease with unique and characteristic features.

Ariga T.

Allergol Int. 2012 Jun;61(2):183-9. doi: 10.2332/allergolint.11-RAI-0412. Epub 2012 Feb 25. Review.

5.

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.

PMID:
11442475
6.

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 Jan-Mar;48(1):66-8.

PMID:
16562789
7.

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. doi: 10.1007/s12185-010-0644-3. Epub 2010 Aug 4.

PMID:
20683686
8.

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. doi: 10.1111/tri.12583. Epub 2015 Apr 30.

9.

Analysis of clinical and molecular characteristics of Wiskott-Aldrich syndrome in 24 patients from 23 unrelated Chinese families.

Zhang ZY, Xiao HQ, Jiang LP, Zhou Y, Zhao Q, Yu J, Liu W, Yang XQ, Zhao XD.

Pediatr Allergy Immunol. 2010 May;21(3):522-32. doi: 10.1111/j.1399-3038.2010.00996.x.

PMID:
20546529
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. doi: 011.04/ijaai.345348.

11.

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 26;355(17):1790-3.

12.

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.

PMID:
17390083
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 1;56(7):1127-9. doi: 10.1002/pbc.22920. Epub 2011 Feb 10.

PMID:
21488158
14.

Wiskott-Aldrich syndrome.

Notarangelo LD, Miao CH, Ochs HD.

Curr Opin Hematol. 2008 Jan;15(1):30-6. Review.

PMID:
18043243
15.

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.

PMID:
9683546
16.

[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. Chinese.

PMID:
22338148
17.

Mutations of the Wiskott-Aldrich Syndrome Protein affect protein expression and dictate the clinical phenotypes.

Ochs HD.

Immunol Res. 2009;44(1-3):84-8. doi: 10.1007/s12026-008-8084-3. Review.

PMID:
19082760
18.

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.

19.

The Wiskott-Aldrich syndrome.

Ochs HD, Thrasher AJ.

J Allergy Clin Immunol. 2006 Apr;117(4):725-38; quiz 739. Review.

PMID:
16630926
20.

Phenotypic and genotypic correction of WASP gene mutation in Wiskott-Aldrich syndrome by unrelated cord blood stem cell transplantation.

Lee YH, Lim YJ, Shin SA, Song CH, Jo EK, Jung JA, Lee HB.

J Korean Med Sci. 2009 Aug;24(4):751-4. doi: 10.3346/jkms.2009.24.4.751. Epub 2009 Jul 30.

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