Griscelli C - Search Results

1

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

2

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

3

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.

4

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. Among authors: griscelli c. Ann Hematol. 1991 Aug;63(2):107-10. doi: 10.1007/BF01707282. Ann Hematol. 1991. PMID: 1912030

5

Prenatal diagnosis of severe combined immunodeficiency and X-linked agammaglobulinemia.

Durandy A, Griscelli C. Durandy A, et al. Among authors: griscelli c. Birth Defects Orig Artic Ser. 1983;19(3):125-7. Birth Defects Orig Artic Ser. 1983. PMID: 6606444 No abstract available.

6

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: griscelli c. Immunodeficiency. 1993;4(1-4):253-8. Immunodeficiency. 1993. PMID: 8167713 No abstract available.

7

A retrospective single-center study of clinical presentation and outcome in 117 patients with severe combined immunodeficiency.

Stephan JL, Vlekova V, Le Deist F, De Saint Basile G, Donadieu J, Durandy A, Blanche S, Griscelli C, Fischer A. Stephan JL, et al. Among authors: griscelli c. Immunodeficiency. 1993;4(1-4):87-8. Immunodeficiency. 1993. PMID: 8167742 No abstract available.

8

Prenatal diagnosis of syndromes associating albinism and immune deficiencies (Chediak-Higashi syndrome and variant).

Durandy A, Breton-Gorius J, Guy-Grand D, Dumez C, Griscelli C. Durandy A, et al. Among authors: griscelli c. Prenat Diagn. 1993 Jan;13(1):13-20. doi: 10.1002/pd.1970130104. Prenat Diagn. 1993. PMID: 8446567

9

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: griscelli c. Am J Hum Genet. 1990 May;46(5):906-11. Am J Hum Genet. 1990. PMID: 1971143 Free PMC article.

10

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: griscelli c. J Clin Invest. 1991 Apr;87(4):1352-9. doi: 10.1172/JCI115139. J Clin Invest. 1991. PMID: 2010548 Free PMC article.

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