Griscelli C - Search Results

1

Two complementation groups account for most cases of inherited MHC class II deficiency.

Lisowska-Grospierre B, Fondaneche MC, Rols MP, Griscelli C, Fischer A. Lisowska-Grospierre B, et al. Among authors: griscelli c. Hum Mol Genet. 1994 Jun;3(6):953-8. doi: 10.1093/hmg/3.6.953. Hum Mol Genet. 1994. PMID: 7951244

2

Combined immunodeficiency with abnormal expression of MHC class II genes.

Griscelli C, Lisowska-Grospierre B, Le Deist F, Durandy A, Marcadet A, Fischer A, de Preval C, Mach B. Griscelli C, et al. Clin Immunol Immunopathol. 1989 Jan;50(1 Pt 2):S140-8. doi: 10.1016/0090-1229(89)90121-9. Clin Immunol Immunopathol. 1989. PMID: 2463126

3

Combined immunodeficiency with defective expression in MHC class II genes.

Griscelli C, Lisowska-Grospierre B, Mach B. Griscelli C, et al. Immunodefic Rev. 1989;1(2):135-53. Immunodefic Rev. 1989. PMID: 2517209 Review.

4

Bone marrow transplantation in major histocompatibility complex class II deficiency: a single-center study of 19 patients.

Klein C, Cavazzana-Calvo M, Le Deist F, Jabado N, Benkerrou M, Blanche S, Lisowska-Grospierre B, Griscelli C, Fischer A. Klein C, et al. Among authors: griscelli c. Blood. 1995 Jan 15;85(2):580-7. Blood. 1995. PMID: 7812013 Free article. Review.

5

Clinical consequences and treatment of primary immunodeficiency syndromes characterized by functional T and B lymphocyte anomalies (combined immune deficiency).

Berthet F, Le Deist F, Duliege AM, Griscelli C, Fischer A. Berthet F, et al. Among authors: griscelli c. Pediatrics. 1994 Feb;93(2):265-70. Pediatrics. 1994. PMID: 8121739

6

Major histocompatibility complex class II deficiency: clinical manifestations, immunologic features, and outcome.

Klein C, Lisowska-Grospierre B, LeDeist F, Fischer A, Griscelli C. Klein C, et al. Among authors: griscelli c. J Pediatr. 1993 Dec;123(6):921-8. doi: 10.1016/s0022-3476(05)80388-9. J Pediatr. 1993. PMID: 8229525

7

Fine mapping of the human SCIDX1 locus at Xq12-13.1.

Markiewicz S, DiSanto JP, Chelly J, Fairweather N, Le Marec B, Griscelli C, Graeber MB, Müller U, Fischer A, Monaco AP, et al. Markiewicz S, et al. Among authors: griscelli c. Hum Mol Genet. 1993 Jun;2(6):651-4. doi: 10.1093/hmg/2.6.651. Hum Mol Genet. 1993. PMID: 8353486

8

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

9

Structural analysis of low TCR-CD3 complex expression in T cells of an immunodeficient patient.

Thoenes G, Soudais C, le Deist F, Griscelli C, Fischer A, Lisowska-Grospierre B. Thoenes G, et al. Among authors: griscelli c. J Biol Chem. 1992 Jan 5;267(1):487-93. J Biol Chem. 1992. PMID: 1370449 Free article.

10

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: griscelli c. 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.

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