de Saint Basile G - Search Results

1

Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B.

Wiszniewski W, Fondaneche MC, Lambert N, Masternak K, Picard C, Notarangelo L, Schwartz K, Bal J, Reith W, Alcaide C, de Saint Basile G, Fischer A, Lisowska-Grospierre B. Wiszniewski W, et al. Among authors: de saint basile g. Immunogenetics. 2000 Apr;51(4-5):261-7. doi: 10.1007/s002510050619. Immunogenetics. 2000. PMID: 10803838

2

Control of human B cell tumor growth in severe combined immunodeficiency mice by monoclonal anti-B cell antibodies.

Durandy A, Brousse N, Rozenberg F, De Saint Basile G, Fischer AM, Fischer A. Durandy A, et al. Among authors: de saint basile g. J Clin Invest. 1992 Sep;90(3):945-52. doi: 10.1172/JCI115971. J Clin Invest. 1992. PMID: 1326002 Free PMC article.

3

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. J Clin Invest. 1992 Mar;89(3):861-6. doi: 10.1172/JCI115665. J Clin Invest. 1992. PMID: 1347296 Free PMC article.

4

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. Hum Genet. 1992 May;89(2):223-8. doi: 10.1007/BF00217127. Hum Genet. 1992. PMID: 1350264 Clinical Trial.

5

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: de saint basile g. Am J Med Genet. 1992 Jul 15;43(5):885-7. doi: 10.1002/ajmg.1320430527. Am J Med Genet. 1992. PMID: 1642281

6

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. Immunol Today. 1991 Dec;12(12):456-61. doi: 10.1016/0167-5699(91)90019-p. Immunol Today. 1991. PMID: 1686172 Review.

7

Primary membrane T cell immunodeficiencies.

Le Deist F, de Saint Basile G, Mazerolles F, Thoenes G, De Villartay JP, Cerf-Bensussan N, Lisowska-Grospierre B, Griscelli C, Fischer A. Le Deist F, et al. Among authors: de villartay jp, de saint basile g. Clin Immunol Immunopathol. 1991 Nov;61(2 Pt 2):S56-60. doi: 10.1016/s0090-1229(05)80038-8. Clin Immunol Immunopathol. 1991. PMID: 1834382 Review.

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. Ann Hematol. 1991 Aug;63(2):107-10. doi: 10.1007/BF01707282. Ann Hematol. 1991. PMID: 1912030

9

Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

Arveiler B, de Saint-Basile G, Fischer A, Griscelli C, Mandel JL. Arveiler B, et al. Among authors: de saint basile g. Am J Hum Genet. 1990 May;46(5):906-11. Am J Hum Genet. 1990. PMID: 1971143 Free PMC article.

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: de villartay jp. 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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