De Saint Basile G - Search Results

1

Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.

Tezcan I, Ersoy F, Sanal O, Turul T, Uckan D, Balci S, Hicsonmez G, Prieur M, Caillat-Zucmann S, Le Deist F, De Saint Basile G. Tezcan I, et al. Among authors: de saint basile g. J Pediatr. 2005 Jan;146(1):137-40. doi: 10.1016/j.jpeds.2004.09.010. J Pediatr. 2005. PMID: 15644840

2

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Ménasché G, Gürgey A, Berkel I, de Saint Basile G. Sanal O, et al. Among authors: de saint basile g. J Clin Immunol. 2002 Jul;22(4):237-43. doi: 10.1023/a:1016045026204. J Clin Immunol. 2002. PMID: 12148598

3

Severe combined immunodeficiency: a retrospective single-center study of clinical presentation and outcome in 117 patients.

Stephan JL, Vlekova V, Le Deist F, Blanche S, Donadieu J, De Saint-Basile G, Durandy A, Griscelli C, Fischer A. Stephan JL, et al. Among authors: de saint basile g. J Pediatr. 1993 Oct;123(4):564-72. doi: 10.1016/s0022-3476(05)80951-5. J Pediatr. 1993. PMID: 8410508

4

T-lymphocyte differentiation and proliferation in the absence of the cytoplasmic tail of the common cytokine receptor gamma c chain in a severe combined immune deficiency X1 patient.

Morelon E, Dautry-Varsat A, Le Deist F, Hacein-Bay S, Fischer A, de Saint Basile G. Morelon E, et al. Among authors: de saint basile g. Blood. 1996 Sep 1;88(5):1708-17. Blood. 1996. PMID: 8781427 Free article.

5

Long-term chimerism and B-cell function after bone marrow transplantation in patients with severe combined immunodeficiency with B cells: A single-center study of 22 patients.

Haddad E, Le Deist F, Aucouturier P, Cavazzana-Calvo M, Blanche S, De Saint Basile G, Fischer A. Haddad E, et al. Among authors: de saint basile g. Blood. 1999 Oct 15;94(8):2923-30. Blood. 1999. PMID: 10515898 Free article.

6

Gene therapy of severe combined immunodeficiencies.

Fischer A, Hacein-Bey S, Le Deist F, Soudais C, Di Santo JP, de Saint Basile G, Cavazzana-Calvo M. Fischer A, et al. Among authors: de saint basile g. Immunol Rev. 2000 Dec;178:13-20. doi: 10.1034/j.1600-065x.2000.17806.x. Immunol Rev. 2000. PMID: 11213798 Review.

7

[Gene therapy of severe combined immunodeficiencies].

Cavazzana-Calvo M, Hacein-Bey S, de Saint-Basile G, Le Deist F, Fischer A. Cavazzana-Calvo M, et al. Among authors: de saint basile g. Transfus Clin Biol. 2000 Jun;7(3):259-60. Transfus Clin Biol. 2000. PMID: 10919216 Review. French. No abstract available.

8

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. Ménasché G, et al. Among authors: de saint basile g. J Clin Invest. 2003 Aug;112(3):450-6. doi: 10.1172/JCI18264. J Clin Invest. 2003. PMID: 12897212 Free PMC article.

9

Early and prolonged intravenous immunoglobulin replacement therapy in childhood agammaglobulinemia: a retrospective survey of 31 patients.

Quartier P, Debré M, De Blic J, de Sauverzac R, Sayegh N, Jabado N, Haddad E, Blanche S, Casanova JL, Smith CI, Le Deist F, de Saint Basile G, Fischer A. Quartier P, et al. Among authors: de blic j, de saint basile g, de sauverzac r. J Pediatr. 1999 May;134(5):589-96. doi: 10.1016/s0022-3476(99)70246-5. J Pediatr. 1999. PMID: 10228295

10

Gene therapy for human severe combined immunodeficiencies.

Fischer A, Hacein-Bey S, Le Deist F, de Saint Basile G, Cavazzana-Calvo M. Fischer A, et al. Among authors: de saint basile g. Immunity. 2001 Jul;15(1):1-4. doi: 10.1016/s1074-7613(01)00175-3. Immunity. 2001. PMID: 11485732 Free article. Review. No abstract available.

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