Giraud G - Search Results

1

[Discovery, in neonatal screening, of 2 families carrying a syndrome of generalized resistance to thyroid hormones].

Poitrineau P, Malpuech G, Nivelon JL, Huet F, Giraud G, François C, Carla H, Loriette Y. Poitrineau P, et al. Among authors: giraud g. Ann Pediatr (Paris). 1993 Sep;40(7):396-403. Ann Pediatr (Paris). 1993. PMID: 8239390 French.

2

[Prenatal diagnosis of X-linked adrenal hypoplasia associated with glycerol kinase deficiency].

Malpuech G, Dastugue B, Giraud G, Jouanel P, Vanlieferinghen P, Carla H. Malpuech G, et al. Among authors: giraud g. J Genet Hum. 1989 Jun;37(2):155-62. J Genet Hum. 1989. PMID: 2545811 French.

3

Genetic homogeneity of Pelizaeus-Merzbacher disease: tight linkage to the proteolipoprotein locus in 16 affected families. PMD Clinical Group.

Boespflug-Tanguy O, Mimault C, Melki J, Cavagna A, Giraud G, Pham Dinh D, Dastugue B, Dautigny A. Boespflug-Tanguy O, et al. Among authors: giraud g. Am J Hum Genet. 1994 Sep;55(3):461-7. Am J Hum Genet. 1994. PMID: 7915877 Free PMC article.

4

Dinucleotide repeat polymorphism in the proteolipoprotein (PLP) gene.

Mimault C, Cailloux F, Giraud G, Dastugue B, Boespflug-Tanguy O. Mimault C, et al. Among authors: giraud g. Hum Genet. 1995 Aug;96(2):236. doi: 10.1007/BF00207388. Hum Genet. 1995. PMID: 7635479

5

Molecular study of the retrovirus-like transposable element 412, a 20-OH ecdysone responsive repetitive sequence in Drosophila cultured cells.

Micard D, Couderc JL, Sobrier ML, Giraud G, Dastugue B. Micard D, et al. Among authors: giraud g. Nucleic Acids Res. 1988 Jan 25;16(2):455-70. doi: 10.1093/nar/16.2.455. Nucleic Acids Res. 1988. PMID: 2829128 Free PMC article.

6

Proteolipoprotein gene analysis in 82 patients with sporadic Pelizaeus-Merzbacher Disease: duplications, the major cause of the disease, originate more frequently in male germ cells, but point mutations do not. The Clinical European Network on Brain Dysmyelinating Disease.

Mimault C, Giraud G, Courtois V, Cailloux F, Boire JY, Dastugue B, Boespflug-Tanguy O. Mimault C, et al. Among authors: giraud g. Am J Hum Genet. 1999 Aug;65(2):360-9. doi: 10.1086/302483. Am J Hum Genet. 1999. PMID: 10417279 Free PMC article.

7

[Polymorphism of DNA in renal polycystosis].

Giraud G, Deteix P, Cluzel P, Gazuy N, Dastugue B, Baguet JC. Giraud G, et al. Presse Med. 1988 Apr 16;17(14):698. Presse Med. 1988. PMID: 2966959 French. No abstract available.

8

Genotype-phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations. Clinical European Network on Brain Dysmyelinating Disease.

Cailloux F, Gauthier-Barichard F, Mimault C, Isabelle V, Courtois V, Giraud G, Dastugue B, Boespflug-Tanguy O. Cailloux F, et al. Among authors: giraud g. Eur J Hum Genet. 2000 Nov;8(11):837-45. doi: 10.1038/sj.ejhg.5200537. Eur J Hum Genet. 2000. PMID: 11093273

9

Actin gene expression is modulated by ecdysterone in a Drosophila cell line.

Couderc JL, Sobrier ML, Giraud G, Becker JL, Dastugue B. Couderc JL, et al. Among authors: giraud g. J Mol Biol. 1983 Mar 5;164(3):419-30. doi: 10.1016/0022-2836(83)90059-1. J Mol Biol. 1983. PMID: 6302276

10

Unusual segregation of cystic fibrosis allele to males.

Kitzis A, Chomel JC, Kaplan JC, Giraud G, Labbe A, Dastugue B, Dumur V, Farriaux JP, Roussel P, Williamson R, et al. Kitzis A, et al. Among authors: giraud g. Nature. 1988 May 19;333(6170):215. doi: 10.1038/333215a0. Nature. 1988. PMID: 3368001 No abstract available.

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