CDKL5-Related Disorders: From Clinical Description to Molecular Genetics

Por Bahi-Buisson, N., Bienvenu, T.
Publicado em 2012

FOXG1-Related Disorders: From Clinical Description to Molecular Genetics

Por Florian, C., Bahi-Buisson, N., Bienvenu, T.
Publicado em 2012

Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

Por Nectoux, J, Fichou, Y, Rosas-Vargas, H, Cagnard, N, Bahi-Buisson, N, Nusbaum, P, Letourneur, F, Chelly, J, Bienvenu, T
Publicado em 2010

Updating the profile of C-terminal MECP2 deletions in Rett syndrome

Por Bebbington, A, Percy, A, Christodoulou, J, Ravine, D, Ho, G, Jacoby, P, Anderson, A, Pineda, M, Ben Zeev, B, Bahi-Buisson, N, Smeets, E, Leonard, H
Publicado em 2009

Kinetic Analyses Guide the Therapeutic Decision in a Novel Form of Moderate Aromatic Acid Decarboxylase Deficiency

Por Barth, M., Serre, V., Hubert, L., Chaabouni, Y., Bahi-Buisson, N., Cadoudal, M., Rabier, D., Tich, S. Nguyen The, Ribeiro, M., Ricquier, D., Munnich, A., Bonneau, D., de Lonlay, P., Christa, L.
Publicado em 2011