1. M. Theaudin, P. Couvert, E. Fournier, D. Bouige, E. Bruckert, P. Perrotte, Y. Vaschalde, T. Maisonobe, D. Bonnefont-Rousselot, A. Carrie, and N. Le Forestier. Lewis-Sumner syndrome and Tangier disease. Arch Neurol, 65(7):968-70, 2008. Note: Journal ArticleUnited States. [WWW]



2. F. Bloch, J. L. Houeto, S. Tezenas du Montcel, F. Bonneville, F. Etchepare, M. L. Welter, S. Rivaud-Pechoux, V. Hahn-Barma, T. Maisonobe, C. Behar, J. Y. Lazennec, E. Kurys, I. Arnulf, A. M. Bonnet, and Y. Agid. Parkinson's disease with camptocormia. J Neurol Neurosurg Psychiatry, 77(11):1223-8, 2006. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Aged, Basal Ganglia/physiopathology, Dystonia/*etiology/physiopathology, Electromyography, Electrophysiology, Female, Humans, Male, Middle Aged, Muscle, Skeletal/pathology, Parkinson Disease/*complications/*physiopathology, *Posture, Prospective Studies, Walking.



3. M. Caer, K. Viala, R. Levy, T. Maisonobe, F. Chochon, A. Lombes, and Y. Agid. Adult-onset chorea and mitochondrial cytopathy. Mov Disord, 20(4):490-2, 2005. Note: Case ReportsJournal ArticleUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Adult, Age of Onset, Biopsy, Cerebrospinal Fluid Proteins/metabolism, Chorea/genetics/metabolism/*pathology, Cognition Disorders/diagnosis, DNA Mutational Analysis, Female, Humans, Male, Mitochondrial Diseases/genetics/metabolism/*pathology, Muscle Fibers, Fast-Twitch/metabolism/pathology, Muscle, Skeletal/metabolism/pathology, Neuropsychological Tests.



4. I. Le Ber, M. Martinez, D. Campion, A. Laquerriere, C. Betard, G. Bassez, C. Girard, P. Saugier-Veber, G. Raux, N. Sergeant, P. Magnier, T. Maisonobe, B. Eymard, C. Duyckaerts, A. Delacourte, T. Frebourg, and D. Hannequin. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. Brain, 127(Pt 9):1979-92, 2004. Note: Journal ArticleEnglanda journal of neurology. [WWW] Keyword(s): Adult, Age of Onset, Aged, Chromosome Mapping/methods, Chromosomes, Human, Pair 15/*genetics, Dementia/complications/*genetics/pathology, Female, Humans, Linkage (Genetics)/genetics, Magnetic Resonance Imaging, Male, Middle Aged, Muscle Weakness/etiology/genetics/pathology, Muscle, Skeletal/pathology, Myosin Heavy Chains/analysis, Myotonic Disorders/complications/*genetics/pathology, Pedigree, Phenotype, RNA-Binding Proteins/genetics, Sex Ratio, tau Proteins/analysis.



5. K. Aure, D. Sternberg, T. Maisonobe, S. Herson, C. Jardel, P. Blondy, A. Lombes, B. Eymard, and P. Laforet. [Myopathy-lipomatosis associated with A8344G mitochondrial DNA mutation]. Rev Neurol (Paris), 159(12):1163-8, 2003. Note: Case ReportsEnglish AbstractJournal ArticleFrance. [WWW] Keyword(s): *Adenine, DNA, Mitochondrial/*genetics, Female, *Guanine, Humans, Lipomatosis/*genetics, Lysine/genetics, Male, Middle Aged, Muscular Diseases/*genetics, Mutation, RNA, Transfer/genetics.



6. N. Birouk, H. Azzedine, O. Dubourg, M. P. Muriel, A. Benomar, T. Hamadouche, T. Maisonobe, R. Ouazzani, A. Brice, M. Yahyaoui, T. Chkili, and E. Le Guern. Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. Arch Neurol, 60(4):598-604, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Charcot-Marie-Tooth Disease/*ethnology/*genetics/pathology, Child, Preschool, Consanguinity, DNA Mutational Analysis, Electrophysiology, Female, Genes, Recessive/*genetics, Humans, Infant, Lod Score, Male, Morocco/ethnology, *Mutation, Pedigree, Phenotype, Serine/genetics.

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