Zobrazeno 1 - 10 of 11 pro vyhledávání: '"MESH: Motor Neuron Disease"'
1
Evidence-Based Treatment Of Chronic Immune-Mediated Neuropathies
Autor: Laurent Magy, Jean-Michel Vallat
Publikováno v: Expert Opinion on Pharmacotherapy
Expert Opinion on Pharmacotherapy, Taylor & Francis, 2009, 10 (11), pp.1741-54. ⟨10.1517/14656560903036095⟩
International audience; Immune-mediated neuropathies are treatable disorders that can result in considerable disability in some cases. Chronic immune-mediated neuropathies include chronic inflammatory demyelinating polyradiculoneuropathy, multifocal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f03d94d339c24fe4f49269f12daa70b
https://doi.org/10.1517/14656560903036095
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2
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study
Autor: Valérie Hahn-Barma, Bruno Dubois, Jean-Charles Lambert, Dominique Campion, Serge Bakchine, Agnès Camuzat, Christine Van Broeckhoven, Serge Belliard, Michèle Puel, Patrice Verpillat, Eric Guedj, Alexis Brice, Fabienne Clot, Marie-Odile Habert, Isabelle Le Ber, Jacqueline Mikol, Pascal Lejeune, Ftd-Mnd, Julie van der Zee, Mustapha Ghanim, Didier Hannequin, Vincent Deramecourt, Christian Meyrignac, Martine Vercelletto, Anne Rovelet-Lecrux, Florence Pasquier, Lucette Lacomblez, Vincent de La Sayette
Publikováno v: Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2008, 131 (Pt 3), pp.732-46. ⟨10.1093/brain/awn012⟩
Brain-A Journal of Neurology, 2008, 131 (Pt 3), pp.732-46. ⟨10.1093/brain/awn012⟩
Brain
Frontotemporal dementia (FTD), characterized by behavioural and language disorders, is a clinically, genetically and pathologically heterogeneous group of diseases. The most recently identified of the four known genes is GRN, associated with 17q-link
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e07accc721ca43c87e20b564df45d077
https://doi.org/10.1093/brain/awn012
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3
New advances in the field of motor neuron diseases
Autor: Philippe Couratier
Publikováno v: Revue Neurologique
Revue Neurologique, Elsevier Masson, 2017, 173 (5), pp.243. ⟨10.1016/j.neurol.2017.04.005⟩
International audience
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d74c3e2fe8f91db7146fd4239fb2e65
https://doi.org/10.1016/j.neurol.2017.04.005
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4
Juvenile and adult-onset ALS/MND among Africans: incidence, phenotype, survival: a review
Autor: Marin, Benoît, Kacem, Imen, Diagana, Mouhamadou, Boulesteix, Marion, Gouider, Riadh, Preux, Pierre-Marie, Couratier, Philippe, Renseigné, Non
Publikováno v: Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders, Taylor & Francis, 2012, 13 (3), pp.276-83. ⟨10.3109/17482968.2011.648644⟩
International audience; AIM: We reviewed the epidemiology of ALS among subjects of African origin, considering incidence, phenotype and prognosis. METHODS: We searched Medline, Scopus, Science direct, Bibliothèque Virtuelle de Neurologie Africaine (
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6a6da8fbb1870e389a24195761d6e2c
https://hal-unilim.archives-ouvertes.fr/hal-00920819
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5
Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease
Autor: I, Le Ber, A, Camuzat, E, Berger, D, Hannequin, A, Laquerrière, 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, A, Brice, Patrice, Verpillat
Publikováno v: Neurology
Neurology, American Academy of Neurology, 2009, 72 (19), pp.1669-76. ⟨10.1212/WNL.0b013e3181a55f1c⟩
International audience; BACKGROUND: Frontotemporal dementia associated with motor neuron disease (FTD-MND) is a rare neurodegenerative disorder that may be inherited by autosomal dominant trait. No major gene has been identified but a locus was mappe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f4546e73894c1b8372182a1ec0bc15
https://pubmed.ncbi.nlm.nih.gov/19433740
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6
TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration
Autor: Lina, Benajiba, Isabelle, Le Ber, Agnès, Camuzat, Mathieu, Lacoste, Catherine, Thomas-Anterion, Philippe, Couratier, Solenn, Legallic, François, Salachas, Didier, Hannequin, Marielle, Decousus, Lucette, Lacomblez, Eric, Guedj, Véronique, Golfier, William, Camu, Bruno, Dubois, Dominique, Campion, Vincent, Meininger, Alexis, Brice
Publikováno v: Annals of Neurology
Annals of Neurology, Wiley, 2009, 65 (4), pp.470-3. ⟨10.1002/ana.21612⟩
International audience; TDP-43 (TAR-DNA binding protein) aggregates in neuronal inclusions in motoneuron disease (MND), as well as in frontotemporal lobar degeneration (FTLD) and FTLD associated with MND (FTLD-MND). Mutations in TARDBP gene, coding f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcffb3d5e87e64f7a8b3c81a3a2f7a79
https://hal.archives-ouvertes.fr/hal-00407819
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7
Low intensity exercise attenuates disease progression and stimulates cell proliferation in the spinal cord of a mouse model with progressive motor neuronopathy
Autor: Ann Catherine Kato, Rime Madani, Florence E. Perrin, Marcel Ferrer-Alcón, Carine Winkler-Hirt
Publikováno v: Neuroscience
Neuroscience, Elsevier-International Brain Research Organization, 2008, 152 (2), pp.291-5. ⟨10.1016/j.neuroscience.2007.11.058⟩
Neuroscience, Vol. 152, No 2 (2008) pp. 291-5
International audience; Physical exercise has been shown to stimulate neurogenesis, increase resistance to brain trauma and disease, improve learning and increase levels of growth factors. We show that low intensity exercise has profound effects on t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9522a83293206da48b6b764afb40ce74
https://www.hal.inserm.fr/inserm-00349510
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8
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration
Autor: Abdelmadjid Hamri, Paulo Alegria, Mathieu Anheim, Alexander Lossos, Masatoyo Nishizawa, Kiyoshi Iwabuchi, Cyril Goizet, José Leal Loureiro, Christel Depienne, Paula Coutinho, Florence Pasquier, Anne Kjersti Erichsen, Amir Boukhris, Vítor Tedim Cruz, Sylvie Forlani, Chokri Mhiri, Jeremy Truchetto, Filippo M. Santorelli, Alexandra Durr, Paola S. Denora, Christine Tranchant, Isabelle Le Ber, José Vale, Imed Feki, Hamid Azzedine, Giovanni Stevanin, Soreya Belarbi, Israela Lerer, G. Uyanik, Vardiela Meiner, Guillaume Garrigues, Alberto Luis Rosa, Alexis Brice, Chantal M. E. Tallaksen, Meriem Tazir, Masayoshi Tada, Victoria Gonzalez-Martinez, Didier Hannequin
Publikováno v: Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2008, 131 (Pt 3), pp.772-84. ⟨10.1093/brain/awm293⟩
Brain-A Journal of Neurology, 2008, 131 (Pt 3), pp.772-84. ⟨10.1093/brain/awm293⟩
Hereditary spastic paraplegias (HSP) are neurodegenerative diseases mainly characterized by lower limb spasticity associated, in complicated forms, with additional neurological signs. We have analysed a large series of index patients (n = 76) with th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d79fa5b64a4221a238025fb00e39148
https://hal.archives-ouvertes.fr/hal-00281713
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9
Progressive motor neuronopathy: a critical role of the tubulin chaperone TBCE in axonal tubulin routing from the Golgi apparatus
Autor: Jean-Louis Guénet, Georg Haase, Natalia Martin, Michael K. E. Schaefer, Henning Schmalbruch, C. Lopez, Emmanuelle Buhler
Publikováno v: Journal of Neuroscience
Journal of Neuroscience, 2007, 27 (33), pp.8779-89. ⟨10.1523/JNEUROSCI.1599-07.2007⟩
Journal of Neuroscience, Society for Neuroscience, 2007, 27 (33), pp.8779-89. ⟨10.1523/JNEUROSCI.1599-07.2007⟩
Axonal degeneration represents one of the earliest pathological features in motor neuron diseases. We here studied the underlying molecular mechanisms in progressive motor neuronopathy (pmn) mice mutated in the tubulin-specific chaperone TBCE. We dem
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c597103e87c59039529d8a57b94d13e6
https://www.hal.inserm.fr/inserm-00195963
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10
[Analysis of reasons for the late diagnosis of amyotrophic lateral sclerosis]
Autor: Torny, F., Lacoste, M., Nguyen, J. M., Tymoczko-Nguyen, M. E., Couratier, Philippe
Publikováno v: Revue Neurologique
Revue Neurologique, Elsevier Masson, 2006, 162 (5), pp.617-22
International audience; INTRODUCTION: The mean diagnostic delay of amyotrophic lateral sclerosis (ALS) is greater than one year. Its causes are multiple, related to the affection, the patient, or medical practices. METHODS: An investigation was carri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e00019931f8a1cc7dd2d26fb6b107c65
https://hal.archives-ouvertes.fr/hal-00354968
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