de Saint Basile G - Search Results

1

Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells.

Stephan V, Wahn V, Le Deist F, Dirksen U, Broker B, Müller-Fleckenstein I, Horneff G, Schroten H, Fischer A, de Saint Basile G. Stephan V, et al. Among authors: de saint basile g. N Engl J Med. 1996 Nov 21;335(21):1563-7. doi: 10.1056/NEJM199611213352104. N Engl J Med. 1996. PMID: 8900089 Free article. No abstract available.

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

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

5

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.

6

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.

7

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

8

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.

9

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.

10

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. Lancet. 1989 Dec 2;2(8675):1319-21. doi: 10.1016/s0140-6736(89)91920-x. Lancet. 1989. PMID: 2574264

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