Nadia Bahi Buisson
AuthID: R-00F-H79
1
TÃTULO: Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly
AUTORES: Catherine Fallet Bianco; Annie Laquerriere; Karine Poirier; Ferechte Razavi; Fabien Guimiot; Patricia Dias; Laurence Loeuillet; Karine Lascelles; Cherif Beldjord; Nathalie Carion; Aurelie Toussaint; Nicole Revencu; Marie Claude Addor; Benoit Lhermitte; Marie Gonzales; Jelena Martinovich; Bettina Bessieres; Maryse Marcy Bonniere; Frederique Jossic; Pascale Marcorelles; ...Mais
PUBLICAÇÃO: 2014, FONTE: ACTA NEUROPATHOLOGICA COMMUNICATIONS, VOLUME: 2
AUTORES: Catherine Fallet Bianco; Annie Laquerriere; Karine Poirier; Ferechte Razavi; Fabien Guimiot; Patricia Dias; Laurence Loeuillet; Karine Lascelles; Cherif Beldjord; Nathalie Carion; Aurelie Toussaint; Nicole Revencu; Marie Claude Addor; Benoit Lhermitte; Marie Gonzales; Jelena Martinovich; Bettina Bessieres; Maryse Marcy Bonniere; Frederique Jossic; Pascale Marcorelles; ...Mais
PUBLICAÇÃO: 2014, FONTE: ACTA NEUROPATHOLOGICA COMMUNICATIONS, VOLUME: 2
INDEXADO EM: 
WOS
WOS2
TÃTULO: GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Full Text
AUTORES: Nadia Bahi Buisson; Karine Poirier; Nathalie Boddaert; Catherine Fallet Bianco; Nicola Specchio; Enrico Bertini; Okay Caglayan; Karine Lascelles; Caroline Elie; Jerome Rambaud; Michel Baulac; Isabelle An; Patricia Dias; Vincent des Portes; Marie Laure Moutard; Christine Soufflet; Monique El Maleh; Cherif Beldjord; Laurent Villard; Jamel Chelly;
PUBLICAÇÃO: 2010, FONTE: BRAIN, VOLUME: 133, NÚMERO: 11
AUTORES: Nadia Bahi Buisson; Karine Poirier; Nathalie Boddaert; Catherine Fallet Bianco; Nicola Specchio; Enrico Bertini; Okay Caglayan; Karine Lascelles; Caroline Elie; Jerome Rambaud; Michel Baulac; Isabelle An; Patricia Dias; Vincent des Portes; Marie Laure Moutard; Christine Soufflet; Monique El Maleh; Cherif Beldjord; Laurent Villard; Jamel Chelly;
PUBLICAÇÃO: 2010, FONTE: BRAIN, VOLUME: 133, NÚMERO: 11
INDEXADO EM: 
Scopus WOS
Scopus WOS3
TÃTULO: Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder Full Text
AUTORES: Wilhelmina G Leen; Joerg Klepper; Marcel M Verbeek; Maike Leferink; Tom Hofste; Baziel G van Engelen; Ron A Wevers; Todd Arthur; Nadia Bahi Buisson; Diana Ballhausen; Jolita Bekhof; Patrick van Bogaert; Ines Carrilho; Brigitte Chabrol; Michael P Champion; James Coldwell; Peter Clayton; Elizabeth Donner; Athanasios Evangeliou; Friedrich Ebinger; ...Mais
PUBLICAÇÃO: 2010, FONTE: BRAIN, VOLUME: 133, NÚMERO: 3
AUTORES: Wilhelmina G Leen; Joerg Klepper; Marcel M Verbeek; Maike Leferink; Tom Hofste; Baziel G van Engelen; Ron A Wevers; Todd Arthur; Nadia Bahi Buisson; Diana Ballhausen; Jolita Bekhof; Patrick van Bogaert; Ines Carrilho; Brigitte Chabrol; Michael P Champion; James Coldwell; Peter Clayton; Elizabeth Donner; Athanasios Evangeliou; Friedrich Ebinger; ...Mais
PUBLICAÇÃO: 2010, FONTE: BRAIN, VOLUME: 133, NÚMERO: 3
