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Articles by B Chabrol (3)

Exhaustive analysis of BH4 and dopamine biosynthesis genes in patients with Dopa-responsive dystonia

F Clot, D Grabli, C Cazeneuve, E Roze, P Castelnau, B Chabrol, P Landrieu, K Nguyen, G Ponsot, M Abada, D Doummar, P Damier, R Gil, S Thobois, A. J Ward, M Hutchinson, A Toutain, F Picard, A Camuzat, E Fedirko, C San, D Bouteiller, E LeGuern, A Durr, M Vidailhet, A Brice and the French Dystonia Network

Brain 132 ( 7 ): 1753 - 1763 , 2009

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

M Anheim, B Monga, M Fleury, P Charles, C Barbot, M Salih, J. P Delaunoy, M Fritsch, L Arning, M Synofzik, L Schols, J Sequeiros, C Goizet, C Marelli, I Le Ber, J Koht, J Gazulla, J De Bleecker, M Mukhtar, N Drouot, L Ali Pacha, T Benhassine, M Chbicheb, A M'Zahem, A Hamri, B Chabrol, J Pouget, R Murphy, M Watanabe, P Coutinho, M Tazir, A Durr, A Brice, C Tranchant and M. Koenig

Brain 132 ( 10 ): 2688 - 2698 , 2009

Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder

W. G Leen, J Klepper, M. M Verbeek, M Leferink, T Hofste, B. G van Engelen, R. A Wevers, T Arthur, N Bahi Buisson, D Ballhausen, J Bekhof, P van Bogaert, I Carrilho, B Chabrol, M. P Champion, J Coldwell, P Clayton, E Donner, A Evangeliou, F Ebinger, K Farrell, R. J Forsyth, C. G. E. L de Goede, S Gross, S Grunewald, H Holthausen, S Jayawant, K Lachlan, V Laugel, K Leppig, M. J Lim, G Mancini, A. D Marina, L Martorell, J McMenamin, M. E. C Meuwissen, H Mundy, N. O Nilsson, A Panzer, B. T Poll The, C Rauscher, C. M. R Rouselle, I Sandvig, T Scheffner, E Sheridan, N Simpson, P Sykora, R Tomlinson, J Trounce, D Webb, B Weschke, H Scheffer and M. A. Willemsen

Brain 133 ( 3 ): 655 - 670 , 2010