Unusual T cell clones in a patient with Nijmegen breakage syndrome.

Por Stoppa-Lyonnet, D, Girault, D, LeDeist, F, Aurias, A
Publicado em 1992

Dissociation between onset of natural killer E-rosette forming cells and of T3-positive cells following HLA-mismatched T cell depleted bone marrow transplantation.

Por De Villartay, J P, Le Deist, F, Griscelli, C, Fischer, A
Publicado em 1987

Numbers of T cell receptor (TCR) alpha beta+ but not of TcR gamma delta+ intraepithelial lymphocytes correlate with the grade of villous atrophy in coeliac patients on a long term...

Por Kutlu, T, Brousse, N, Rambaud, C, Le Deist, F, Schmitz, J, Cerf-Bensussan, N
Publicado em 1993

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...

Por Milili, M, Le Deist, F, de Saint-Basile, G, Fischer, A, Fougereau, M, Schiff, C
Publicado em 1993

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

Por de Saint-Basile, G, Le Deist, F, Caniglia, M, Lebranchu, Y, Griscelli, C, Fischer, A
Publicado em 1992

B cell immunodeficiency, distal limb abnormalities, and urogenital malformations in a three generation family: a novel autosomal dominant syndrome?

Por Edery, P., Le Deist, F., Briard, M., Debre, M., Munnich, A., Griscelli, C., Fischer, A., Lyonnet, S.
Publicado em 2001

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

Por Meffre, E, LeDeist, F, de Saint-Basile, G, Deville, A, Fougereau, M, Fischer, A, Schiff, C
Publicado em 1996

Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)

Por Arkwright, P D, Rieux-Laucat, F, Le Deist, F, Stevens, R F, Angus, B, Cant, A J
Publicado em 2000

Increased radiosensitivity of granulocyte macrophage colony-forming units and skin fibroblasts in human autosomal recessive severe combined immunodeficiency.

Por Cavazzana-Calvo, M, Le Deist, F, De Saint Basile, G, Papadopoulo, D, De Villartay, J P, Fischer, A
Publicado em 1993

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.

Por Rieux-Laucat, F, Bahadoran, P, Brousse, N, Selz, F, Fischer, A, Le Deist, F, De Villartay, J P
Publicado em 1998

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

Por de Saint-Basile, G, Le Deist, F, de Villartay, J P, Cerf-Bensussan, N, Journet, O, Brousse, N, Griscelli, C, Fischer, A
Publicado em 1991

Deficiency of the adhesive protein complex lymphocyte function antigen 1, complement receptor type 3, glycoprotein p150,95 in a girl with recurrent bacterial infections. Effects on...

Por Fischer, A, Seger, R, Durandy, A, Grospierre, B, Virelizier, J L, Le Deist, F, Griscelli, C, Fischer, E, Kazatchkine, M, Bohler, M C
Publicado em 1985

The antibody spectrum in individuals with defect expression of HLA class II and the LFA-1 glycoprotein family genes.

Por Smith, C I, Bremard-Oury, C, Le Deist, F, Griscelli, C, Aucouturier, P, Möller, G, Hammarström, L, Preud'homme, J L, Weening, R S
Publicado em 1988

Linkage of familial hemophagocytic lymphohistiocytosis to 10q21-22 and evidence for heterogeneity.

Por Dufourcq-Lagelouse, R, Jabado, N, Le Deist, F, Stéphan, J L, Souillet, G, Bruin, M, Vilmer, E, Schneider, M, Janka, G, Fischer, A, de Saint Basile, G
Publicado em 1999

Physical mapping by FISH of the DiGeorge critical region (DGCR): Involvement of the region in familial cases

Por Desmaze, C., Prieur, M., Amblard, F., Aïkem, M., LeDeist, F., Demczuk, S., Zucman, J., Plougastel, B., Delattre, O., Croquette, M.-F., Brevière, G.-M., Huon, C., Le Merrer, M., Mathieu, M., Sidi, D., Stephan, J.-L., Aurias, A.
Publicado em 1993