1. I. Le Ber, A. Camuzat, E. Berger, D. Hannequin, A. Laquerriere, V. Golfier, D. Seilhean, G. Viennet, P. Couratier, P. Verpillat, S. Heath, W. Camu, O. Martinaud, L. Lacomblez, M. Vercelletto, F. Salachas, F. Sellal, M. Didic, C. Thomas-Anterion, M. Puel, B. F. Michel, C. Besse, C. Duyckaerts, V. Meininger, D. Campion, B. Dubois, and A. Brice. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Neurology, 72(19):1669-76, 2009. Note: French Research Network on FTD/FTD-MNDJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



2. I. Le Ber, A. Camuzat, J. van der Zee, D. Hannequin, F. Pasquier, I. Gijselinck, D. Campion, M. Puel, A. Laquerriere, T. De Pooter, M. Van den Broeck, B. Dubois, F. Sellal, L. Lacomblez, M. Vercelletto, C. Thomas-Anterion, B. F. Michel, V. Golfier, M. Didic, F. Salachas, C. Duyckaerts, J. C. Lambert, M. Cruts, P. Verpillat, C. Van Broeckhoven, and A. Brice. PGRN gene mutations in both sporadic and familial frontotemporal dementia. Neurology, 68(12):A351-A351, 2007. Note: Suppl. 1. [WWW]



3. I. Le Ber, J. van der Zee, D. Hannequin, I. Gijselinck, D. Campion, M. Puel, A. Laquerriere, T. De Pooter, A. Camuzat, M. Van den Broeck, B. Dubois, F. Sellal, L. Lacomblez, M. Vercelletto, C. Thomas-Anterion, B. F. Michel, V. Golfier, M. Didic, F. Salachas, C. Duyckaerts, M. Cruts, P. Verpillat, C. Van Broeckhoven, and A. Brice. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Hum Mutat, 28(9):846-55, 2007. Note: French Research Network on FTD/FTD-MNDJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



4. L. Guyant-Marechal, A. Laquerriere, C. Duyckaerts, C. Dumanchin, J. Bou, F. Dugny, I. Le Ber, T. Frebourg, D. Hannequin, and D. Campion. Valosin-containing protein gene mutations: clinical and neuropathologic features. Neurology, 67(4):644-51, 2006. Note: Journal ArticleUnited States. [WWW] Keyword(s): Cell Cycle Proteins/*genetics, Chromosome Disorders/epidemiology/*genetics, DNA Mutational Analysis, Dementia/epidemiology/*genetics, Female, France/epidemiology, Genetic Predisposition to Disease/epidemiology/genetics, Heterozygote, Humans, Incidence, Male, Middle Aged, Multiple Organ Failure/epidemiology/*genetics, Mutation, Myositis, Inclusion Body/epidemiology/*genetics, Osteitis Deformans/epidemiology/*genetics, Pedigree, Prevalence, Retrospective Studies, Risk Assessment/*methods, Risk Factors, Syndrome.



5. A. Rovelet-Lecrux, D. Hannequin, G. Raux, N. Le Meur, A. Laquerriere, A. Vital, C. Dumanchin, S. Feuillette, A. Brice, M. Vercelletto, F. Dubas, T. Frebourg, and D. Campion. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nat Genet, 38(1):24-6, 2006. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Age of Onset, Alzheimer Disease/epidemiology/*genetics/pathology, Amyloid beta-Protein/analysis/*genetics, Brain/*pathology, Case-Control Studies, Cerebral Amyloid Angiopathy/epidemiology/*genetics/pathology, Female, *Gene Duplication, Genes, Dominant, Humans, Male, Microsatellite Repeats, Polymerase Chain Reaction/methods.



6. O. Martinaud, A. Laquerriere, L. Guyant-Marechal, P. Ahtoy, P. Vera, N. Sergeant, A. Camuzat, P. Bourgeois, J. J. Hauw, D. Campion, and D. Hannequin. Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. Acta Neuropathol (Berl), 110(1):84-92, 2005. Note: Case ReportsJournal ArticleGermany. [WWW] Keyword(s): Blotting, Western, Brain/metabolism/*pathology, Dementia/complications/genetics/*pathology, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Motor Neuron Disease/complications/genetics/*pathology, Nerve Tissue Proteins/genetics, Pedigree, Spinal Cord/metabolism/*pathology, Superoxide Dismutase/genetics, Tauopathies/genetics/metabolism/*pathology, tau Proteins/metabolism.



7. 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.



8. N. Girardot, B. Allinquant, D. Langui, A. Laquerriere, B. Dubois, J. J. Hauw, and C. Duyckaerts. Accumulation of flotillin-1 in tangle-bearing neurones of Alzheimer's disease. Neuropathol Appl Neurobiol, 29(5):451-61, 2003. Note: Comparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Aged, Aged, 80 and over, Alzheimer Disease/metabolism/*pathology, Biological Markers/analysis, Blotting, Western, Brain/metabolism/*pathology, Female, Fluorescent Antibody Technique, Humans, Immunohistochemistry, Male, Membrane Microdomains/chemistry, Membrane Proteins/*metabolism, Microscopy, Confocal, Neurofibrillary Tangles/*metabolism/pathology, Neurons/*pathology, tau Proteins/metabolism.

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