Fischer A - Search Results

1

Close linkage of the locus for X chromosome-linked severe combined immunodeficiency to polymorphic DNA markers in Xq11-q13.

de Saint Basile G, Arveiler B, Oberlé I, Malcolm S, Levinsky RJ, Lau YL, Hofker M, Debre M, Fischer A, Griscelli C, et al. de Saint Basile G, et al. Among authors: fischer a. Proc Natl Acad Sci U S A. 1987 Nov;84(21):7576-9. doi: 10.1073/pnas.84.21.7576. Proc Natl Acad Sci U S A. 1987. PMID: 3478714 Free PMC article.

2

Genetic study of a new X-linked recessive immunodeficiency syndrome.

de Saint-Basile G, Le Deist F, Caniglia M, Lebranchu Y, Griscelli C, Fischer A. de Saint-Basile G, et al. Among authors: fischer a. J Clin Invest. 1992 Mar;89(3):861-6. doi: 10.1172/JCI115665. J Clin Invest. 1992. PMID: 1347296 Free PMC article.

3

Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.

de Saint Basile G, Arveiler B, Fraser NJ, Boyd Y, Graig IW, Griscelli G, Fischer A. de Saint Basile G, et al. Among authors: fischer a. Lancet. 1989 Dec 2;2(8675):1319-21. doi: 10.1016/s0140-6736(89)91920-x. Lancet. 1989. PMID: 2574264

4

Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells.

DiSanto JP, Rieux-Laucat F, Dautry-Varsat A, Fischer A, de Saint Basile G. DiSanto JP, et al. Among authors: fischer a. Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9466-70. doi: 10.1073/pnas.91.20.9466. Proc Natl Acad Sci U S A. 1994. PMID: 7937790 Free PMC article.

5

Wiskott-Aldrich syndrome carrier detection with the hypervariable marker M27 beta.

de Saint Basile G, Notarangelo LD, Bonaiti-Pellié C, Doussau M, Prolini O, Craig IW, Ugazio A, Griscelli C, Fischer A. de Saint Basile G, et al. Among authors: fischer a. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

6

Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.

Journet O, Durandy A, Doussau M, Le Deist F, Couvreur J, Griscelli C, Fischer A, de Saint-Basile G. Journet O, et al. Among authors: fischer a. Am J Med Genet. 1992 Jul 15;43(5):885-7. doi: 10.1002/ajmg.1320430527. Am J Med Genet. 1992. PMID: 1642281

7

X-linked immunodeficiencies: clues to genes involved in T- and B-cell differentiation.

de Saint Basile G, Fischer A. de Saint Basile G, et al. Among authors: fischer a. Immunol Today. 1991 Dec;12(12):456-61. doi: 10.1016/0167-5699(91)90019-p. Immunol Today. 1991. PMID: 1686172 Review.

There are five major human X-linked immunodeficiencies, each with a characteristic impairment of T-and/or B-cell differentiation. The molecular bases of these diseases remain unknown but, as Genevieve de Saint Basile and Alain Fischer report, major steps towards tha …

There are five major human X-linked immunodeficiencies, each with a characteristic impairment of T-and/or B-cell differentiation. The …

8

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. De Saint-Basile G, et al. Among authors: fischer a. Ann Hematol. 1991 Aug;63(2):107-10. doi: 10.1007/BF01707282. Ann Hematol. 1991. PMID: 1912030

9

European experience of bone-marrow transplantation for severe combined immunodeficiency.

Fischer A, Landais P, Friedrich W, Morgan G, Gerritsen B, Fasth A, Porta F, Griscelli C, Goldman SF, Levinsky R, et al. Fischer A, et al. Lancet. 1990 Oct 6;336(8719):850-4. doi: 10.1016/0140-6736(90)92348-l. Lancet. 1990. PMID: 1976883

10

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).

de Saint-Basile G, Le Deist F, de Villartay JP, Cerf-Bensussan N, Journet O, Brousse N, Griscelli C, Fischer A. de Saint-Basile G, et al. Among authors: fischer a. J Clin Invest. 1991 Apr;87(4):1352-9. doi: 10.1172/JCI115139. J Clin Invest. 1991. PMID: 2010548 Free PMC article.

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