Zobrazeno 1 - 10
of 914
pro vyhledávání: '"A. Bruneteau"'
Autor:
D. De Bels, C. Pierrakos, A. Bruneteau, F. Reul, Q. Crevecoeur, N. Marrone, D. Vissenaeken, G. Borgers, C. Balestra, P. M. Honoré, S. Theunissen
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
ObjectiveTo observe the effects of a fast-acute ascent to high altitude on brain cognitive function and transcranial doppler parameters in order to understand the physiological countermeasures of hypoxia.Methods17 high-altitude-naïve male subjects (
Externí odkaz:
https://doaj.org/article/cfd1a5f1314d46f0beb95178c37dbe58
Autor:
Vincent Huin, David Blum, Violette Delforge, Emeline Cailliau, Sofia Djeziri, Kathy Dujardin, Alexandre Genet, Romain Viard, Shahram Attarian, Gaelle Bruneteau, Julien Cassereau, Steeve Genestet, Anne-Laure Kaminsky, Marie-Hélène Soriani, Mathilde Lefilliatre, Philippe Couratier, Sophie Pittion-Vouyovitch, Florence Esselin, Elisa De La Cruz, Nathalie Guy, Ivan Kolev, Philippe Corcia, Pascal Cintas, Claude Desnuelle, Luc Buée, Véronique Danel-Brunaud, David Devos, Anne-Sophie Rolland
Publikováno v:
Neurobiology of Disease, Vol 199, Iss , Pp 106603- (2024)
Caffeine consumption outcomes on Amyotrophic Lateral Sclerosis (ALS) including progression, survival and cognition remain poorly defined and may depend on its metabolization influenced by genetic variants. 378 ALS patients with a precise evaluation o
Externí odkaz:
https://doaj.org/article/972ce4d8410148ae8d535f49c2d84219
Autor:
Anne-Sophie Montero, Ilyes Aliouat, Matthieu Ribon, Michael Canney, Lauriane Goldwirt, Samia Mourah, Félix Berriat, Christian S. Lobsiger, Pierre-François Pradat, François Salachas, Gaëlle Bruneteau, Alexandre Carpentier, Séverine Boillée
Publikováno v:
EBioMedicine, Vol 106, Iss , Pp 105235- (2024)
Summary: Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by a progressive loss of motor neurons. The limited efficacy of recent therapies in clinical development may be linked to lack of drug penetra
Externí odkaz:
https://doaj.org/article/829c21513bc04088ba5edb899d13fb89
Autor:
Huin, Vincent, Blum, David, Delforge, Violette, Cailliau, Emeline, Djeziri, Sofia, Dujardin, Kathy, Genet, Alexandre, Viard, Romain, Attarian, Shahram, Bruneteau, Gaelle, Cassereau, Julien, Genestet, Steeve, Kaminsky, Anne-Laure, Soriani, Marie-Hélène, Lefilliatre, Mathilde, Couratier, Philippe, Pittion-Vouyovitch, Sophie, Esselin, Florence, De La Cruz, Elisa, Guy, Nathalie, Kolev, Ivan, Corcia, Philippe, Cintas, Pascal, Desnuelle, Claude, Buée, Luc, Danel-Brunaud, Véronique, Devos, David, Rolland, Anne-Sophie
Publikováno v:
In Neurobiology of Disease September 2024 199
Autor:
Montero, Anne-Sophie, Aliouat, Ilyes, Ribon, Matthieu, Canney, Michael, Goldwirt, Lauriane, Mourah, Samia, Berriat, Félix, Lobsiger, Christian S., Pradat, Pierre-François, Salachas, François, Bruneteau, Gaëlle, Carpentier, Alexandre, Boillée, Séverine
Publikováno v:
In eBioMedicine August 2024 106
Publikováno v:
In Revue Neurologique November 2023 179(9):967-974
Autor:
Mirella El Khoury, Olivier Biondi, Gaelle Bruneteau, Delphine Sapaly, Sabrina Bendris, Cynthia Bezier, Zoé Clerc, Elias Abi Akar, Laure Weill, Assaad A. Eid, Frédéric Charbonnier
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
IntroductionSpinal muscular atrophy (SMA) is a fatal neurodegenerative disorder, characterized by motor neuron (MN) degeneration and severe muscular atrophy and caused by Survival of Motor Neuron (SMN) depletion. Therapies aimed at increasing SMN in
Externí odkaz:
https://doaj.org/article/b187f5fb340440b7ab9572622915223a
Autor:
Hesters, A., Bruneteau, G.
Publikováno v:
In Pratique Neurologique - FMC March 2023 14(1):55-60
Autor:
Maria-Belen Lopez-Herdoiza, Stephanie Bauché, Baptiste Wilmet, Caroline Le Duigou, Delphine Roussel, Magali Frah, Jonas Béal, Gabin Devely, Susana Boluda, Petra Frick, Delphine Bouteiller, Sébastien Dussaud, Pierre Guillabert, Carine Dalle, Magali Dumont, Agnes Camuzat, Dario Saracino, Mathieu Barbier, Gaelle Bruneteau, Phillippe Ravassard, Manuela Neumann, Sophie Nicole, Isabelle Le Ber, Alexis Brice, Morwena Latouche
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 17 (2023)
The GGGGCC intronic repeat expansion within C9ORF72 is the most common genetic cause of ALS and FTD. This mutation results in toxic gain of function through accumulation of expanded RNA foci and aggregation of abnormally translated dipeptide repeat p
Externí odkaz:
https://doaj.org/article/cf47ec065e0e43cbbe6e3408fa24d68b
Autor:
Laura Le Gall, William J. Duddy, Cecile Martinat, Virginie Mariot, Owen Connolly, Vanessa Milla, Ekene Anakor, Zamalou G. Ouandaogo, Stephanie Millecamps, Jeanne Lainé, Udaya Geetha Vijayakumar, Susan Knoblach, Cedric Raoul, Olivier Lucas, Jean Philippe Loeffler, Peter Bede, Anthony Behin, Helene Blasco, Gaelle Bruneteau, Maria Del Mar Amador, David Devos, Alexandre Henriques, Adele Hesters, Lucette Lacomblez, Pascal Laforet, Timothee Langlet, Pascal Leblanc, Nadine Le Forestier, Thierry Maisonobe, Vincent Meininger, Laura Robelin, Francois Salachas, Tanya Stojkovic, Giorgia Querin, Julie Dumonceaux, Gillian Butler Browne, Jose‐Luis González De Aguilar, Stephanie Duguez, Pierre Francois Pradat
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 13, Iss 2, Pp 1385-1402 (2022)
Abstract Background The cause of the motor neuron (MN) death that drives terminal pathology in amyotrophic lateral sclerosis (ALS) remains unknown, and it is thought that the cellular environment of the MN may play a key role in MN survival. Several
Externí odkaz:
https://doaj.org/article/261a53bffa414819a14cb82060834ea9