Zobrazeno 1 - 10
of 631
pro vyhledávání: '"Maues de Paula, A."'
Autor:
Lou Grangeon, Camille Charbonnier, Aline Zarea, Stephane Rousseau, Anne Rovelet-Lecrux, David Bendetowicz, Marion Lemaitre, Cécile Malrain, Muriel Quillard-Muraine, Kevin Cassinari, David Maltete, Jeremie Pariente, Olivier Moreaud, Eloi Magnin, Benjamin Cretin, Marie-Anne Mackowiak, Adeline Rollin Sillaire, Martine Vercelletto, Elsa Dionet, Olivier Felician, Pauline Rod-Olivieri, Catherine Thomas-Antérion, Gaelle Godeneche, Mathilde Sauvée, Leslie Cartz-Piver, Isabelle Le Ber, Valérie Chauvire, Therèse Jonveaux, Anna-Chloé Balageas, Annie Laquerriere, Charles Duyckaerts, Anne Vital, Andre Maues de Paula, David Meyronet, Lucie Guyant-Marechal, Didier Hannequin, Elisabeth Tournier-Lasserve, Dominique Campion, CNR-MAJ collaborators, Gaël Nicolas, David Wallon
Publikováno v:
Alzheimer’s Research & Therapy, Vol 15, Iss 1, Pp 1-12 (2023)
Abstract Background APP duplication is a rare genetic cause of Alzheimer disease and cerebral amyloid angiopathy (CAA). We aimed to evaluate the phenotypes of APP duplications carriers. Methods Clinical, radiological, and neuropathological features o
Externí odkaz:
https://doaj.org/article/88847a664cd34093ae31f3d54233ce99
Autor:
Ait-El-Mkadem Saadi, Samira, Kaphan, Elsa, Morales Jaurrieta, Amaya, Fragaki, Konstantina, Chaussenot, Annabelle, Bannwarth, Sylvie, Maues De Paula, André, Paquis-Flucklinger, Véronique, Rouzier, Cécile
Publikováno v:
In European Journal of Medical Genetics December 2022 65(12)
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Externí odkaz:
https://doaj.org/article/c14a995b479046868d2975b78fcc1256
Autor:
Delteil, Clémence, Meyronet, David, Maues de Paula, Andre, Jouvet, Anne, Piercecchi-Marti, Marie-Dominique
Publikováno v:
In Annales de Pathologie April 2018 38(2):103-109
Autor:
Miguel Lopez-Cuina, Pierre-Olivier Fernagut, Marie-Hélène Canron, Anne Vital, Béatrice Lannes, André Maues De Paula, Nathalie Streichenberger, Dominique Guehl, Philippe Damier, Alexandre Eusebio, Jean-Luc Houeto, François Tison, Christine Tranchant, François Viallet, Tatiana Witjas, Stéphane Thobois, Wassilios G. Meissner
Publikováno v:
Neurobiology of Disease, Vol 118, Iss , Pp 155-160 (2018)
Slowly progressive, levodopa-responsive multiple system atrophy (MSA) may be misdiagnosed as Parkinson's disease (PD). Deep brain stimulation (DBS) is mostly ineffective in these patients and may even worsen the clinical course. Here we assessed whet
Externí odkaz:
https://doaj.org/article/f3663a0168b54928898c5793c76142d9
Autor:
Meissner, Wassilios G., Laurencin, Chloé, Tranchant, Christine, Witjas, Tatiana, Viallet, François, Guehl, Dominique, Damier, Philippe, Houeto, Jean-Luc, Tison, François, Eusebio, Alexandre, Vital, Anne, Streichenberger, Nathalie, Lannes, Béatrice, Maues de Paula, André, Thobois, Stéphane
Publikováno v:
In Parkinsonism and Related Disorders March 2016 24:69-75
Autor:
Béhin, A., Salort-Campana, E., Wahbi, K., Richard, P., Carlier, R.-Y., Carlier, P., Laforêt, P., Stojkovic, T., Maisonobe, T., Verschueren, A., Franques, J., Attarian, S., Maues de Paula, A., Figarella-Branger, D., Bécane, H.-M., Nelson, I., Duboc, D., Bonne, G., Vicart, P., Udd, B., Romero, N., Pouget, J., Eymard, B.
Publikováno v:
In Revue Neurologique October 2015 171(10):715-729
Autor:
Arthur Viodé, Clémence Fournier, Agnès Camuzat, François Fenaille, NeuroCEB Brain Bank, Morwena Latouche, Fanny Elahi, Isabelle Le Ber, Christophe Junot, Foudil Lamari, Vincent Anquetil, François Becher, Franck Letournel, Anne Vital, Françoise Chapon, Catherine Godfraind, Claude-Alain Maurage, Vincent Deramecourt, David Meyronnet, Nathalie Streichenberger, André Maues de Paula, Valérie Rigau, Fanny Vandenbos-Burel, Charles Duyckaerts, Danielle Seilhean, Véronique Sazdovitch, Serge Milin, Dan Christian Chiforeanu, Annie Laquerrière, Béatrice Lannes
Publikováno v:
Frontiers in Neuroscience, Vol 12 (2018)
Frontotemporal dementia (FTD) is a fatal neurodegenerative disease characterized by behavioral and language disorders. The main genetic cause of FTD is an intronic hexanucleotide repeat expansion (G4C2)n in the C9ORF72 gene. A loss of function of the
Externí odkaz:
https://doaj.org/article/cd19437b3505479386a248050a20e764
Autor:
Clémence Delteil, C. Champeaux, Catherine Boval, Georges Leonetti, A. Maues de Paula, Marie-Dominique Piercecchi-Marti, M.-A. Devooght, Lucile Tuchtan
Publikováno v:
La Revue de Médecine Légale. 12:149-153
Summary Focal cortical dysplasia (FCD) is the third leading cause of pharmacoresistant epilepsy diagnosed by epilepsy surgery and is a common malformation of cerebral cortical development. It is marked by abnormalities of cortical lamination, neurona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::700a5573e8b494f029c27789fde568a7
https://doi.org/10.1016/j.medleg.2021.02.008
https://doi.org/10.1016/j.medleg.2021.02.008
Autor:
Deharo, François, Carvelli, Julien, Cautela, Jennifer, Garcia, Maxime, Sarles, Claire, Maues de Paula, Andre, Bourenne, Jérémy, Gainnier, Marc, Bichon, Amandine
Publikováno v:
Journal of Clinical Medicine; Oct2022, Vol. 11 Issue 19, p5611, 14p