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Similar articles for PubMed (Select 7437512)

1.

Wiskott-Aldrich syndrome: cellular impairments and their implication for carrier detection.

Prchal JT, Carroll AJ, Prchal JF, Crist WM, Skalka HW, Gealy WJ, Harley J, Malluh A.

Blood. 1980 Dec;56(6):1048-54.

2.

Wiskott-Aldrich syndrome in a female.

Lutskiy MI, Sasahara Y, Kenney DM, Rosen FS, Remold-O'Donnell E.

Blood. 2002 Oct 15;100(8):2763-8.

3.

[Molecular genetic diagnosis of Wiskott-Aldrich syndrome].

Orth U, Rosenkranz W, Schwinger E, Holzgreve W, Gal A.

Monatsschr Kinderheilkd. 1993 Sep;141(9):728-31. German.

PMID:
8413349
4.
5.
6.

X-linked thrombocytopenia and Wiskott-Aldrich syndrome: similar regional assignment but distinct X-inactivation pattern in carriers.

De Saint-Basile G, Schlegel N, Caniglia M, Le Deist F, Kaplan C, Lecompte T, Piller F, Fischer A, Griscelli C.

Ann Hematol. 1991 Aug;63(2):107-10.

PMID:
1912030
7.

Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a Negro family.

Prasad AS, Tranchida L, Konno ET, Berman L, Albert S, Sing CF, Brewer GJ.

J Clin Invest. 1968 Jun;47(6):1415-24.

8.

Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.

Goodship J, Carter J, Espanol T, Boyd Y, Malcolm S, Levinsky RJ.

Blood. 1991 Jun 15;77(12):2677-81.

9.

[Genetic carrier detection for the Wiskott-Aldrich syndrome using restriction fragment length polymorphism analysis].

de Weers M, Kolvenbag GJ, Versteegde IF, Hendriks RW, Sandkuyl LA, Schuurman RK.

Ned Tijdschr Geneeskd. 1990 May 5;134(18):913-6. Dutch.

PMID:
1971711
10.
11.

Wiskott-Aldrich syndrome in a family with Fanconi anemia.

Rohrer J, Ribeiro RC, Auerbach AD, Mirro B, Conley ME.

J Pediatr. 1996 Jul;129(1):50-5.

PMID:
8757562
12.

Determination of carrier status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wiskott-Aldrich syndrome protein expression in peripheral blood mononuclear cells.

Yamada M, Ariga T, Kawamura N, Yamaguchi K, Ohtsu M, Nelson DL, Kondoh T, Kobayashi I, Okano M, Kobayashi K, Sakiyama Y.

J Immunol. 2000 Jul 15;165(2):1119-22.

13.

Wiskott-Aldrich syndrome in a female with skewed X-chromosome inactivation.

Andreu N, Pujol-Moix N, Martinez-Lostao L, Oset M, Muñiz-Diaz E, Estivill X, Volpini V, Fillat C.

Blood Cells Mol Dis. 2003 Nov-Dec;31(3):332-7.

PMID:
14636648
14.

Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

Notarangelo LD, Parolini O, Porta F, Locatelli F, Lanfranchi A, Marconi M, Nespoli L, Albertini A, Craig IW, Ugazio AG.

Hum Genet. 1991 Dec;88(2):237-41.

PMID:
1684569
15.

[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. Chinese.

PMID:
14744380
16.

The thrombocytopenia of Wiskott Aldrich syndrome is not related to a defect in proplatelet formation.

Haddad E, Cramer E, Rivière C, Rameau P, Louache F, Guichard J, Nelson DL, Fischer A, Vainchenker W, Debili N.

Blood. 1999 Jul 15;94(2):509-18.

17.

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
18.

A defect in hematopoietic stem cell migration explains the nonrandom X-chromosome inactivation in carriers of Wiskott-Aldrich syndrome.

Lacout C, Haddad E, Sabri S, Svinarchouk F, Garçon L, Capron C, Foudi A, Mzali R, Snapper SB, Louache F, Vainchenker W, Duménil D.

Blood. 2003 Aug 15;102(4):1282-9. Epub 2003 May 1.

19.
20.

Missense mutations of the WASP gene cause intermittent X-linked thrombocytopenia.

Notarangelo LD, Mazza C, Giliani S, D'Aria C, Gandellini F, Ravelli C, Locatelli MG, Nelson DL, Ochs HD, Notarangelo LD.

Blood. 2002 Mar 15;99(6):2268-9.

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