Tardieu M - Search Results

1

Autosomal dominant deletions of the mitochondrial genome in a case of progressive encephalomyopathy.

Cormier V, Rotig A, Tardieu M, Colonna M, Saudubray JM, Munnich A. Cormier V, et al. Among authors: tardieu m. Am J Hum Genet. 1991 Apr;48(4):643-8. Am J Hum Genet. 1991. PMID: 2014791 Free PMC article.

2

Cerebellar ataxia and mental retardation in a child with an inherited satellited chromosome 4q.

Faivre L, Radford I, Viot G, Edery P, Munnich A, Tardieu M, Vekemans M. Faivre L, et al. Among authors: tardieu m. Ann Genet. 2000 Jan-Mar;43(1):35-8. doi: 10.1016/s0003-3995(00)00016-2. Ann Genet. 2000. PMID: 10818219

3

Parental origin of the X chromosomes in Rett syndrome.

Benedetti L, Munnich A, Melki J, Tardieu M, Turleau C. Benedetti L, et al. Among authors: tardieu m. Am J Med Genet. 1992 Sep 1;44(1):121-3. doi: 10.1002/ajmg.1320440131. Am J Med Genet. 1992. PMID: 1355631 No abstract available.

4

Persistent mitochondrial dysfunction and perinatal exposure to antiretroviral nucleoside analogues.

Blanche S, Tardieu M, Rustin P, Slama A, Barret B, Firtion G, Ciraru-Vigneron N, Lacroix C, Rouzioux C, Mandelbrot L, Desguerre I, Rötig A, Mayaux MJ, Delfraissy JF. Blanche S, et al. Among authors: tardieu m. Lancet. 1999 Sep 25;354(9184):1084-9. doi: 10.1016/S0140-6736(99)07219-0. Lancet. 1999. PMID: 10509500

5

Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome.

de Pontual L, Mathieu Y, Golzio C, Rio M, Malan V, Boddaert N, Soufflet C, Picard C, Durandy A, Dobbie A, Heron D, Isidor B, Motte J, Newburry-Ecob R, Pasquier L, Tardieu M, Viot G, Jaubert F, Munnich A, Colleaux L, Vekemans M, Etchevers H, Lyonnet S, Amiel J. de Pontual L, et al. Among authors: tardieu m. Hum Mutat. 2009 Apr;30(4):669-76. doi: 10.1002/humu.20935. Hum Mutat. 2009. PMID: 19235238

6

Submicroscopic deletions of 17p13.3 in type 1 Lissencephaly.

Mantel A, Leonard C, Husson B, Miladi N, Tardieu M, Landrieu P. Mantel A, et al. Among authors: tardieu m. Hum Genet. 1994 Jul;94(1):95-6. doi: 10.1007/BF02272851. Hum Genet. 1994. PMID: 8034303

7

MECP2 mutations account for most cases of typical forms of Rett syndrome.

Bienvenu T, Carrié A, de Roux N, Vinet MC, Jonveaux P, Couvert P, Villard L, Arzimanoglou A, Beldjord C, Fontes M, Tardieu M, Chelly J. Bienvenu T, et al. Among authors: tardieu m. Hum Mol Genet. 2000 May 22;9(9):1377-84. doi: 10.1093/hmg/9.9.1377. Hum Mol Genet. 2000. PMID: 10814719

8

Low levels of human immunodeficiency virus replication in the brain tissue of children with severe acquired immunodeficiency syndrome encephalopathy.

Vazeux R, Lacroix-Ciaudo C, Blanche S, Cumont MC, Henin D, Gray F, Boccon-Gibod L, Tardieu M. Vazeux R, et al. Among authors: tardieu m. Am J Pathol. 1992 Jan;140(1):137-44. Am J Pathol. 1992. PMID: 1731520 Free PMC article.

9

Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity.

Feldmann J, Ménasché G, Callebaut I, Minard-Colin V, Bader-Meunier B, Le Clainche L, Fischer A, Le Deist F, Tardieu M, de Saint Basile G. Feldmann J, et al. Among authors: tardieu m. Blood. 2005 Apr 1;105(7):2658-63. doi: 10.1182/blood-2004-09-3590. Epub 2004 Dec 14. Blood. 2005. PMID: 15598808 Free article.

10

[Antiviral agents and mitochondrial diseases].

Tardieu M, Barret B, Blanche S. Tardieu M, et al. Arch Pediatr. 2001 May;8 Suppl 2:327s-328s. doi: 10.1016/s0929-693x(01)80062-2. Arch Pediatr. 2001. PMID: 11394104 French. No abstract available.

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