1. 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. Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. Brain, 132(Pt 10):2688-98, 2009. Note: Journal articlea journal of neurology. [WWW]



2. C. M. Dhaenens, S. Burnouf, C. Simonin, E. Van Brussel, A. Duhamel, L. Defebvre, C. Duru, I. Vuillaume, C. Cazeneuve, P. Charles, P. Maison, S. Debruxelles, C. Verny, H. Gervais, J. P. Azulay, C. Tranchant, A. C. Bachoud-Levi, A. Durr, L. Buee, P. Krystkowiak, B. Sablonniere, and D. Blum. A genetic variation in the ADORA2A gene modifies age at onset in Huntington's disease. Neurobiol Dis, 35(3):474-6, 2009. Note: Huntington French Speaking NetworkJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



3. S. T. du Montcel, P. Charles, P. Ribai, C. Goizet, A. Le Bayon, P. Labauge, L. Guyant-Marechal, S. Forlani, C. Jauffret, N. Vandenberghe, K. N'Guyen, I. Le Ber, D. Devos, C. M. Vincitorio, M. U. Manto, F. Tison, D. Hannequin, M. Ruberg, A. Brice, and A. Durr. Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment. Brain, 131(Pt 5):1352-61, 2008. Note: Journal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tValidation StudiesEnglanda journal of neurology. [WWW] Keyword(s): Adult, Aged, Cerebellar Ataxia/*physiopathology/psychology, Female, Humans, Male, Middle Aged, Neuropsychological Tests, Paraplegia/*physiopathology/psychology, Psychometrics, Psychomotor Disorders/*etiology, Quality of Life, *Severity of Illness Index.



4. P. Charles, A. Camuzat, N. Benammar, F. Sellal, A. Destee, A. M. Bonnet, S. Lesage, I. Le Ber, G. Stevanin, A. Durr, and A. Brice. Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?. Neurology, 2007. Note: French Parkinson's Disease Genetics Study Group*Journal article. [WWW]



5. F. Mochel, P. Charles, F. Seguin, J. Barritault, C. Coussieu, L. Perin, Y. Le Bouc, C. Gervais, G. Carcelain, A. Vassault, J. Feingold, D. Rabier, and A. Durr. Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression. PLoS ONE, 2(7):e647, 2007. Note: Journal ArticleUnited States. [WWW]



6. P. Ribai, F. Pousset, M. L. Tanguy, S. Rivaud-Pechoux, I. Le Ber, F. Gasparini, P. Charles, A. S. Beraud, M. Schmitt, M. Koenig, A. Mallet, A. Brice, and A. Durr. Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-up. Arch Neurol, 64(4):558-564, 2007. [WWW]



7. M. Schupbach, E. Lohmann, M. Anheim, S. Lesage, V. Czernecki, S. Yaici, Y. Worbe, P. Charles, M. L. Welter, P. Pollak, A. Durr, Y. Agid, and A. Brice. Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations. Mov Disord, 22(1):119-22, 2007. Note: Clinical TrialComparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Adult, Aged, Deep Brain Stimulation/*methods, Female, Glycine/genetics, Humans, Male, Middle Aged, *Mutation, *Parkinsonian Disorders/genetics/pathology/therapy, Protein-Serine-Threonine Kinases/*genetics, Retrospective Studies, Serine/genetics, Subthalamic Nucleus/physiology/*surgery, Threonine/genetics.



8. G. Stevanin, F. M. Santorelli, H. Azzedine, P. Coutinho, J. Chomilier, P. S. Denora, E. Martin, A. M. Ouvrard-Hernandez, A. Tessa, N. Bouslam, A. Lossos, P. Charles, J. L. Loureiro, N. Elleuch, C. Confavreux, V. T. Cruz, M. Ruberg, E. Leguern, D. Grid, M. Tazir, B. Fontaine, A. Filla, E. Bertini, A. Durr, and A. Brice. Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nat Genet, 39(3):366-372, 2007. Note: Journal article. [WWW]



9. I. Coman, G. Barbin, P. Charles, B. Zalc, and C. Lubetzki. Axonal signals in central nervous system myelination, demyelination and remyelination. J Neurol Sci, 233(1-2):67-71, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tReviewNetherlands. [WWW] Keyword(s): Animals, Axons/*pathology, Central Nervous System/metabolism/*pathology, Demyelinating Diseases/*pathology, Humans, Models, Biological, Myelin Sheath/*physiology, Neural Cell Adhesion Molecule L1/metabolism, Neural Inhibition, Sialic Acids/metabolism, *Signal Transduction.



10. G. Barbin, M. S. Aigrot, P. Charles, A. Foucher, M. Grumet, M. Schachner, B. Zalc, and C. Lubetzki. Axonal cell-adhesion molecule L1 in CNS myelination. Neuron Glia Biol, 1(1):65-72, 2004. Note: Journal ArticleEngland. [WWW]



11. G. Barbin, M. S. Aigrot, P. Charles, M. Schachner, M. Grumet, B. Zalc, and C. Lubetzki. Axonal cell adhesion molecule L1 and central nervoyus system myelination. Neuron/Glia Biology, (1):65-72, 2004.

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