1. I. Le Ber, A. Camuzat, D. Hannequin, F. Pasquier, E. Guedj, A. Rovelet-Lecrux, V. Hahn-Barma, J. van der Zee, F. Clot, S. Bakchine, M. Puel, M. Ghanim, L. Lacomblez, J. Mikol, V. Deramecourt, P. Lejeune, V. de la Sayette, S. Belliard, M. Vercelletto, C. Meyrignac, C. Van Broeckhoven, J. C. Lambert, P. Verpillat, D. Campion, M. O. Habert, B. Dubois, and A. Brice. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study. Brain, 131(Pt 3):732-46, 2008. Note: French research network on FTD/FTD-MNDJournal ArticleMulticenter StudyResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adult, Age of Onset, Aged, Aged, 80 and over, Aphasia, Primary Progressive/genetics, Brain/pathology/physiopathology, Brain Mapping/methods, Cognition Disorders/etiology, Dementia/*genetics/pathology/psychology, Disease Progression, Epidemiologic Methods, Female, Heterozygote, Humans, Intercellular Signaling Peptides and Proteins/*genetics, Magnetic Resonance Imaging, Male, Middle Aged, Motor Neuron Disease/genetics, *Mutation, Neuropsychological Tests, Phenotype.



2. O. Moreaud, S. Belliard, J. Snowden, S. Auriacombe, S. Basaglia-Pappas, F. Bernard, L. Bon, J. Boutantin, C. Boutoleau-Bretonniere, A. Charnallet, E. Coutant, D. David, V. Deramecourt, Y. Gaestel, S. Garnier, E. Guichart, V. Hahn-Barma, B. Lebail, C. Lebrun-Givois, E. Lamy, N. Le Carret, B. Lemesle, A. Memin, J. Pariente, F. Pasquier, P. Renou, O. Rouaud, M. Sarazin, C. Thomas-Anterion, M. Vercelletto, and M. E. Virat-Brassaud. [Semantic dementia: reflexions of a French working group for diagnostic criteria and constitution of a patient cohort]. Rev Neurol (Paris), 164(4):343-53, 2008. Note: English AbstractJournal ArticleReviewFrance. [WWW] Keyword(s): Aphasia/etiology/*psychology, Dementia/*diagnosis/physiopathology/*psychology, Diagnostic Imaging, Humans, Neuropsychological Tests, Prosopagnosia/etiology/psychology, Psychomotor Performance/physiology, Terminology as Topic.



3. P. Ribai, C. Depienne, E. Fedirko, A. C. Jothy, C. Viveweger, V. Hahn-Barma, A. Brice, and A. Durr. Mental deficiency in three families with SPG4 spastic paraplegia. Eur J Hum Genet, 16(1):97-104, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tEnglandEjhg. [WWW] Keyword(s): Adenosine Triphosphatases/*genetics, Adult, Amino Acid Substitution, Female, Genes, Dominant, Haplotypes, Humans, Male, Mental Retardation/complications/*genetics, Middle Aged, *Mutation, Mutation, Missense, Pedigree, Phenotype, Point Mutation, Spastic Paraplegia,, Hereditary/complications/*genetics/physiopathology/psychology.



4. P. Ribai, K. Nguyen, V. Hahn-Barma, I. Gourfinkel-An, M. Vidailhet, A. Legout, C. Dode, A. Brice, and A. Durr. Psychiatric and cognitive difficulties as indicators of juvenile huntington disease onset in 29 patients. Arch Neurol, 64(6):813-9, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Atrophy, Brain/pathology, Child, Cognition Disorders/*etiology, Fathers, Female, Humans, Huntington Disease/*diagnosis/genetics/*psychology, Male, Mental Disorders/*etiology/psychology, Mothers, Movement Disorders/etiology, Retrospective Studies, Time Factors, Trinucleotide Repeats.



5. M. Vidailhet, L. Vercueil, J. L. Houeto, P. Krystkowiak, C. Lagrange, J. Yelnik, E. Bardinet, A. L. Benabid, S. Navarro, D. Dormont, S. Grand, S. Blond, C. Ardouin, B. Pillon, K. Dujardin, V. Hahn-Barma, Y. Agid, A. Destee, and P. Pollak. Bilateral, pallidal, deep-brain stimulation in primary generalised dystonia: a prospective 3 year follow-up study. Lancet Neurol, 6(3):223-9, 2007. Note: French SPIDY Study GroupClinical TrialJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Adolescent, Adult, Affect, Age of Onset, Cognition/physiology, *Deep Brain Stimulation, Disability Evaluation, Dystonia/physiopathology/psychology/*therapy, Female, Follow-Up Studies, Globus Pallidus/*physiology, Humans, Magnetic Resonance Imaging, Male, Molecular Chaperones/genetics, Movement/physiology, Neuropsychological Tests, Prospective Studies, Psychiatric Status Rating Scales, Quality of Life, Questionnaires, Treatment Outcome.



6. 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.



7. F. Vinckier, L. Naccache, C. Papeix, J. Forget, V. Hahn-Barma, S. Dehaene, and L. Cohen. ``What'' and ``where'' in word reading: ventral coding of written words revealed by parietal atrophy. J Cogn Neurosci, 18(12):1998-2012, 2006. Note: Journal ArticleUnited States. [WWW]



8. S. Klebe, A. Durr, A. Rentschler, V. Hahn-Barma, M. Abele, N. Bouslam, L. Schols, P. Jedynak, S. Forlani, E. Denis, C. Dussert, Y. Agid, P. Bauer, C. Globas, U. Wullner, A. Brice, O. Riess, and G. Stevanin. New mutations in protein kinase Cgamma associated with spinocerebellar ataxia type 14. Ann Neurol, 58(5):720-9, 2005. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Aged, Aged, 80 and over, DNA Mutational Analysis, Electromyography/methods, Exons, Family Health, Female, Humans, Magnetic Resonance Imaging/methods, Male, Middle Aged, Molecular Structure, *Mutation, Pedigree, Phenotype, *Polymorphism, Genetic, Protein Kinase C/*genetics, Spinocerebellar Ataxias/*genetics/pathology/physiopathology.



9. A. Slachevsky, J. M. Villalpando, M. Sarazin, V. Hahn-Barma, B. Pillon, and B. Dubois. Frontal assessment battery and differential diagnosis of frontotemporal dementia and Alzheimer disease. Arch Neurol, 61(7):1104-7, 2004. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Aged, Aged, 80 and over, Alzheimer Disease/*diagnosis/*psychology, Brief Psychiatric Rating Scale/statistics & numerical data, Dementia/*diagnosis/metabolism/*psychology, Diagnosis, Differential, Female, Frontal Lobe/metabolism/pathology, Humans, Male, Middle Aged.



10. C. M. Tallaksen, E. Guichart-Gomez, P. Verpillat, V. Hahn-Barma, M. Ruberg, B. Fontaine, A. Brice, B. Dubois, and A. Durr. Subtle cognitive impairment but no dementia in patients with spastin mutations. Arch Neurol, 60(8):1113-8, 2003. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adenosine Triphosphatases/*genetics, Adolescent, Adult, Age of Onset, Child, Child, Preschool, *Cognition, DNA Mutational Analysis, *Dementia/genetics, Disease Progression, Female, *Heterozygote, Humans, Infant, Male, Middle Aged, Mutation, Neuropsychological Tests, Spastic Paraplegia, Hereditary/genetics/*physiopathology.

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