Torthaí cuardaigh - Mathieu Barbier

CD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy. de réir Mathieu Barbier, Audrey Sabbagh, Edwige Kasper, Muriel Asheuer, Ornella Ahouansou, Ingrid Pribill, Sonja Forss-Petter, Michel Vidaud, Johannes Berger, Patrick Aubourg

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Platelets alter gene expression profile in human brain endothelial cells in an in vitro model of cerebral malaria. de réir Mathieu Barbier, Dorothée Faille, Béatrice Loriod, Julien Textoris, Claire Camus, Denis Puthier, Laurence Flori, Samuel Crocodile Wassmer, Geneviève Victorero, Marie-Christine Alessi, Thierry Fusaï, Catherine Nguyen, Georges E Grau, Pascal Rihet

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Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias de réir Clémence Fournier, Vincent Anquetil, Agnès Camuzat, Sandrine Stirati-Buron, Véronique Sazdovitch, Laura Molina-Porcel, Sabrina Turbant, Daisy Rinaldi, Raquel Sánchez-Valle, Mathieu Barbier, Morwena Latouche, Neuro-CEB Neuropathology Network, Giovanni Stevanin, Danielle Seilhean, Alexis Brice, Charles Duyckaerts, Isabelle Le Ber

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C9ORF72 knockdown triggers FTD-like symptoms and cell pathology in mice de réir Maria-Belen Lopez-Herdoiza, Stephanie Bauché, Baptiste Wilmet, Caroline Le Duigou, Delphine Roussel, Magali Frah, Jonas Béal, Gabin Devely, Susana Boluda, Petra Frick, Delphine Bouteiller, Sébastien Dussaud, Pierre Guillabert, Carine Dalle, Magali Dumont, Agnes Camuzat, Dario Saracino, Mathieu Barbier, Gaelle Bruneteau, Phillippe Ravassard, Manuela Neumann, Manuela Neumann, Sophie Nicole, Isabelle Le Ber, Alexis Brice, Morwena Latouche, Morwena Latouche

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