G. Giraud

发表

Pelizaeus–Merzbacher–Like disease presentation of MCT8 mutated male subjects

B. Dan, R. Touraine, G. De Michele, 2009, Annals of neurology.

Relevance of GJC2 promoter mutation in Pelizaeus‐Merzbacher–like disease

E. Bertini, C. Vaurs-Barrière, O. Boespflug-Tanguy, 2012, Annals of neurology.

Unusual segregation of cystic fibrosis allele to males

B. Dastugue, A. Kitzis, J. Kaplan, 1988, Nature.

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

J. Melki, B. Dastugue, O. Boespflug-Tanguy, 1994, American journal of human genetics.

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

B. Dastugue, O. Boespflug-Tanguy, V. Courtois, 2000, European journal of human genetics : EJHG.

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.

J. Boire, B. Dastugue, O. Boespflug-Tanguy, 1999, American journal of human genetics.

Pleiotropic Specific Responses Induced by Ecdysterone in the Cultured Kc Cells of Drosophila melanogaster

B. Dastugue, F. Péronnet, G. Giraud, 1984 .

Confirmation of linkage disequilibrium between haplotype B (XV-2c, allele 1; KM-19, allele 2) and cystic fibrosis allele in the French population

B. Dastugue, M. Vidaud, A. Kitzis, 2004, Human Genetics.

Hereditary spastic paraplegia caused by the PLP1 ‘rumpshaker mutation’

C. Crone, I. Law, O. Boespflug-Tanguy, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

Genotype–phenotype correlation in inherited brain myelination defects due to proteolipid protein gene mutations

B. Dastugue, O. Boespflug-Tanguy, V. Courtois, 2000, European Journal of Human Genetics.

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

B. Dastugue, G. Giraud, J. Couderc, 1983, Journal of molecular biology.

Neurodegenerative disorder related to AIMP1/p43 mutation is not a PMLD.

C. Vaurs-Barrière, O. Boespflug-Tanguy, C. Sarret, 2011, American journal of human genetics.

Sjögren–Larsson syndrome: Novel mutations in the ALDH3A2 gene in a French cohort

A. Afenjar, R. Wanders, C. Vaurs-Barrière, 2012, Journal of the Neurological Sciences.

Pelizaeus-Merzbacher disease: a frameshift deletion/insertion event in the myelin proteolipid gene.

D. Pham‐Dinh, O. Boespflug-Tanguy, G. Giraud, 1993, Human molecular genetics.

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

B. Dastugue, G. Giraud, J. Couderc, 1988, Nucleic Acids Research.