Le Deist F - Search Results

1

IgH repertoire and Ig-related gene expression in X-linked agammaglobulinemia.

Schiff C, Milili M, Le Deist F, De Saint-Basile G, Fischer A, Fougereau M. Schiff C, et al. Among authors: le deist f. Immunodeficiency. 1993;4(1-4):3-12. Immunodeficiency. 1993. PMID: 8167721 No abstract available.

2

Variant forms of X-linked severe combined immunodeficiency disease: one or many genes?

Disanto JP, Le Deist F, Caniglia M, Markiewicz S, Lebranchu Y, Griscelli C, Fischer A, De Saint-Basile G. Disanto JP, et al. Among authors: le deist f. Immunodeficiency. 1993;4(1-4):253-8. Immunodeficiency. 1993. PMID: 8167713 No abstract available.

3

Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.

Milili M, Le Deist F, de Saint-Basile G, Fischer A, Fougereau M, Schiff C. Milili M, et al. Among authors: le deist f. J Clin Invest. 1993 Apr;91(4):1616-29. doi: 10.1172/JCI116369. J Clin Invest. 1993. PMID: 8473505 Free PMC article.

4

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

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: le deist f. Am J Med Genet. 1992 Jul 15;43(5):885-7. doi: 10.1002/ajmg.1320430527. Am J Med Genet. 1992. PMID: 1642281

6

Genetic analysis of the human CD3-epsilon gene in a T cell receptor/CD3 immunodeficiency.

Soudais C, De Villartay JP, Le Deist F, Fischer A, Lisowska-Grospierre B. Soudais C, et al. Among authors: le deist f. Immunodeficiency. 1993;4(1-4):117-9. Immunodeficiency. 1993. PMID: 8167684 No abstract available.

7

Functional T cell immunodeficiency characterized by defective TCR/CD3 induced tyrosylphosphorylation.

Hivroz C, Le Deist F, Buc HA, Griscelli C, Fischer A. Hivroz C, et al. Among authors: le deist f. Immunodeficiency. 1993;4(1-4):131-2. Immunodeficiency. 1993. PMID: 8167686

8

A human non-XLA immunodeficiency disease characterized by blockage of B cell development at an early proB cell stage.

Meffre E, LeDeist F, de Saint-Basile G, Deville A, Fougereau M, Fischer A, Schiff C. Meffre E, et al. J Clin Invest. 1996 Oct 1;98(7):1519-26. doi: 10.1172/JCI118943. J Clin Invest. 1996. PMID: 8833898 Free PMC article.

9

A non-XLA primary deficiency causes the earliest known defect of B cell differentiation in humans: a comparison with an XLA case.

Meffre E, LeDeist F, de Saint-Basile G, Deville A, Fougereau M, Fischer A, Schiff C. Meffre E, et al. Immunol Lett. 1997 Jun 1;57(1-3):93-9. doi: 10.1016/s0165-2478(97)00052-7. Immunol Lett. 1997. PMID: 9232432

10

Gene therapy of severe combined immunodeficiencies.

Fischer A, Hacein-Bey S, Le Deist F, De Saint Basile G, Cavazzana-Calvo M. Fischer A, et al. Among authors: le deist f. Adv Exp Med Biol. 2001;495:199-204. doi: 10.1007/978-1-4615-0685-0_27. Adv Exp Med Biol. 2001. PMID: 11774567 No abstract available.

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