Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Maria Del Mar Amador"'
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
Autor:
Timothée Lenglet, Jonathan Mirault, Marie Veyrat-Masson, Aurélie Funkiewiez, Maria del Mar Amador, Gaelle Bruneteau, Nadine Le Forestier, Pierre-Francois Pradat, Francois Salachas, Yannick Vacher, Lucette Lacomblez, Jean Lorenceau
Publikováno v:
Frontiers in Neuroscience, Vol 13 (2019)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder causing a progressive motor weakness of all voluntary muscles, whose progression challenges communication modalities such as handwriting or speech. The current study investigated whe
Externí odkaz:
https://doaj.org/article/87a44b4522da4f96abdbf415831a2581
Autor:
Giorgia Querin, Mohamed-Mounir El Mendili, Timothée Lenglet, Anthony Behin, Tanya Stojkovic, François Salachas, David Devos, Nadine Le Forestier, Maria del Mar Amador, Rabab Debs, Lucette Lacomblez, Vincent Meninger, Gaëlle Bruneteau, Julien Cohen-Adad, Stéphane Lehéricy, Pascal Laforêt, Sophie Blancho, Habib Benali, Martin Catala, Menghan Li, Véronique Marchand-Pauvert, Jean-Yves Hogrel, Peter Bede, Pierre-François Pradat
Publikováno v:
NeuroImage: Clinical, Vol 21, Iss , Pp - (2019)
Spinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly progressive lower motor neuron syndromes. Nevertheless, wider cerebral involvement has been consistently reported in mouse models. The objective of this study is the charac
Externí odkaz:
https://doaj.org/article/53e889b333a8466487f9b9fdfd3df598
Autor:
Rabab Debs, Jean-Yves Hogrel, Gaëlle Bruneteau, Nadine Le Forestier, Peter Bede, Pascal Laforêt, Sophie Blancho, Anthony Behin, Timothée Lenglet, Véronique Marchand-Pauvert, François Salachas, Giorgia Querin, Pierre-François Pradat, Tanya Stojkovic, Maria del Mar Amador
Publikováno v:
Journal of Neurology
Journal of Neurology, Springer Verlag, 2021, 268 (5), pp.1792-1802. ⟨10.1007/s00415-020-10332-5⟩
Journal of Neurology, 2021, 268 (5), pp.1792-1802. ⟨10.1007/s00415-020-10332-5⟩
Journal of Neurology, Springer Verlag, 2021, 268 (5), pp.1792-1802. ⟨10.1007/s00415-020-10332-5⟩
Journal of Neurology, 2021, 268 (5), pp.1792-1802. ⟨10.1007/s00415-020-10332-5⟩
International audience; Objective: The aim of this study was the comprehensive characterisation of longitudinal clinical, electrophysiological and neuroimaging measures in type III and IV adult spinal muscular atrophy (SMA) with a view to propose obj
Autor:
Claudia Morelli, Federico Verde, Philip Van Damme, Maria del Mar Amador, Foudil Lamari, Susanne Petri, Koen Poesen, Jochen H. Weishaupt, Jens Kuhle, Markus Otto, Julian Grosskreutz, Elizabeth Gray, Steffen Halbgebauer, Mykyta Kachanov, François Salachas, Petra Steinacker, Vincenzo Silani, Aleksandra Maceski, Nayana Gaur, Martin R Turner, Alexander E Volk, Benjamin Mayer, Albert C. Ludolph, Claude Jardel, Patrick Weydt, Joost Raaphorst, Emily Feneberg, Simon Witzel, Marcel M. Verbeek, Patrick Oeckl
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22, 3-4, pp. 276-286
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22, 276-286
Amyotrophic lateral sclerosis and frontotemporal degeneration, 22(3-4), 276-286. Informa Healthcare
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 22, 276-286
Amyotrophic lateral sclerosis and frontotemporal degeneration, 22(3-4), 276-286. Informa Healthcare
Objective: Levels of chitotriosidase (CHIT1) are increased in the cerebrospinal fluid (CSF) of amyotrophic lateral sclerosis (ALS) patients reflecting microglial activation. Here, we determine the diagnostic and prognostic potential of CHIT1 for earl
Autor:
Alisdair, McNeill, Maria-Del-Mar, Amador, Hilary, Bekker, Angus, Clarke, Ashley, Crook, Cathy, Cummings, Alison, McEwen, Christopher, McDermott, Oliver, Quarrell, Alessandra, Renieri, Jennifer, Roggenbuck, Kristiana, Salmon, Alexander, Volk, Jochen, Weishaupt
Publikováno v:
European journal of human genetics : EJHG. 30(6)
Autor:
Lina Jeantin, Isabelle Plu, Maria del Mar Amador, Elisabeth Maillart, Fanny Lanternier, Valérie Pourcher, Vincent Davy
Publikováno v:
Neurology
Neurology, 2022, 99 (11), pp.475-479. ⟨10.1212/WNL.0000000000200992⟩
Neurology, 2022, 99 (11), pp.475-479. ⟨10.1212/WNL.0000000000200992⟩
Candida spp. myelopathies are very rare. We report a case of subacute longitudinally extensive transverse myelitis in an apparently immunocompetent 55-year-old man. After a negative infectious workup, corticosteroids and plasma exchange were initiate
Autor:
Tessa Kliest, Ruben P.A. Van Eijk, Ammar Al-Chalabi, Alberto Albanese, Peter M. Andersen, Maria Del Mar Amador, Geir BrÅthen, Veronique Brunaud-Danel, Lev Brylev, William Camu, Mamede De Carvalho, Cristina Cereda, Hakan Cetin, Delia Chaverri, Adriano Chiò, Philippe Corcia, Philippe Couratier, Fabiola De Marchi, Claude Desnuelle, Michael A. Van Es, JesÚs Esteban, Massimiliano Filosto, Alberto GarcÍa Redondo, Julian Grosskreutz, Clemens O. Hanemann, Trygve HolmØy, Helle HØyer, Caroline Ingre, Blaz Koritnik, Magdalena Kuzma-Kozakiewicz, Thomas Lambert, Peter N. Leigh, Christian Lunetta, Jessica Mandrioli, Christopher J. Mcdermott, Thomas Meyer, Jesus S. Mora, Susanne Petri, MÓnica Povedano, Evy Reviers, Nilo Riva, Kit C.B. Roes, Miguel Á. Rubio, FranÇois Salachas, Stayko Sarafov, Gianni SorarÙ, Zorica Stevic, Kirsten Svenstrup, Anette Torvin MØller, Martin R. Turner, Philip Van Damme, Lucie A.G. Van Leeuwen, Luis Varona, Juan F. VÁzquez Costa, Markus Weber, Orla Hardiman, Leonard H. Van Den Berg
Publikováno v:
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2022, pp.1-8. ⟨10.1080/21678421.2021.2024856⟩
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23, 481-488
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23, 7-8, pp. 481-488
Kliest, T, Van Eijk, R P A, Al-Chalabi, A, Albanese, A, Andersen, P M, Amador, M D M, BrÅthen, G, Brunaud-Danel, V, Brylev, L, Camu, W, De Carvalho, M, Cereda, C, Cetin, H, Chaverri, D, Chiò, A, Corcia, P, Couratier, P, De Marchi, F, Desnuelle, C, Van Es, M A, Esteban, J, Filosto, M, GarcÍa Redondo, A, Grosskreutz, J, Hanemann, C O, HolmØy, T, HØyer, H, Ingre, C, Koritnik, B, Kuzma-Kozakiewicz, M, Lambert, T, Leigh, P N, Lunetta, C, Mandrioli, J, Mcdermott, C J, Meyer, T, Mora, J S, Petri, S, Povedano, MÓ, Reviers, E, Riva, N, Roes, K C B, Rubio, M, Salachas, F, Sarafov, S, SorarÙ, G, Stevic, Z, Svenstrup, K, MØller, A T, Turner, M R, Van Damme, P, Van Leeuwen, L A G, Varona, L, VÁzquez Costa, J F, Weber, M, Hardiman, O & Van Den Berg, L H 2022, ' Clinical trials in pediatric ALS : a TRICALS feasibility study ', Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol. 23, no. 7-8, pp. 481-488 . https://doi.org/10.1080/21678421.2021.2024856
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 2022, pp.1-8. ⟨10.1080/21678421.2021.2024856⟩
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23, 481-488
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 23, 7-8, pp. 481-488
Kliest, T, Van Eijk, R P A, Al-Chalabi, A, Albanese, A, Andersen, P M, Amador, M D M, BrÅthen, G, Brunaud-Danel, V, Brylev, L, Camu, W, De Carvalho, M, Cereda, C, Cetin, H, Chaverri, D, Chiò, A, Corcia, P, Couratier, P, De Marchi, F, Desnuelle, C, Van Es, M A, Esteban, J, Filosto, M, GarcÍa Redondo, A, Grosskreutz, J, Hanemann, C O, HolmØy, T, HØyer, H, Ingre, C, Koritnik, B, Kuzma-Kozakiewicz, M, Lambert, T, Leigh, P N, Lunetta, C, Mandrioli, J, Mcdermott, C J, Meyer, T, Mora, J S, Petri, S, Povedano, MÓ, Reviers, E, Riva, N, Roes, K C B, Rubio, M, Salachas, F, Sarafov, S, SorarÙ, G, Stevic, Z, Svenstrup, K, MØller, A T, Turner, M R, Van Damme, P, Van Leeuwen, L A G, Varona, L, VÁzquez Costa, J F, Weber, M, Hardiman, O & Van Den Berg, L H 2022, ' Clinical trials in pediatric ALS : a TRICALS feasibility study ', Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol. 23, no. 7-8, pp. 481-488 . https://doi.org/10.1080/21678421.2021.2024856
Background: Pediatric investigation plans (PIPs) describe how adult drugs can be studied in children. In 2015, PIPs for Amyotrophic Lateral Sclerosis (ALS) became mandatory for European marketing-authorization of adult treatments, unless a waiver is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31fe6c6cded34ce9af67049e3ef23c06
https://hal-unilim.archives-ouvertes.fr/hal-03673852
https://hal-unilim.archives-ouvertes.fr/hal-03673852
Autor:
Stéphanie Millecamps, Aude-Marie Grapperon, Serge Lumbroso, François Salachas, Patrick Vourc'h, Aude Chiot, Delphine Bohl, Cécile Cazeneuve, Emilien Bernard, Anne-Laure Fauret-Amsellem, Kevin Mouzat, William Camu, Maria del Mar Amador, Christian S Lobsiger, Philippe Corcia, Beata Gyorgy, Séverine Boillée, Jean-Christophe Antoine, Shahram Attarian, Elisa Teyssou, Annie Verschueren, Yannick Marie, Claire Guissart, Jean-Philippe Camdessanché, Danielle Seilhean, Eric Leguern, François Muratet, Vincent Meininger, Justine Guegan
Publikováno v:
Journal of Neurology, Neurosurgery and Psychiatry
Journal of Neurology, Neurosurgery and Psychiatry, 2021, 92 (9), pp.942-949. ⟨10.1136/jnnp-2020-325921⟩
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2021, 92 (9), pp.942-949. ⟨10.1136/jnnp-2020-325921⟩
Journal of Neurology, Neurosurgery and Psychiatry, 2021, 92 (9), pp.942-949. ⟨10.1136/jnnp-2020-325921⟩
Journal of Neurology, Neurosurgery and Psychiatry, BMJ Publishing Group, 2021, 92 (9), pp.942-949. ⟨10.1136/jnnp-2020-325921⟩
ObjectiveMutations in superoxide dismutase 1 gene (SOD1), encoding copper/zinc superoxide dismutase protein, are the second most frequent high penetrant genetic cause for amyotrophic lateral sclerosis (ALS) motor neuron disease in populations of Euro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af1bcdd954cf21224229083c5d45451d
https://hal.sorbonne-universite.fr/hal-03353407
https://hal.sorbonne-universite.fr/hal-03353407
Autor:
Avi Assouline, Antoine Schernberg, Maria Del Mar Amador, Nadine Le Forestier, Gaëlle Bruneteau, François Salachas, Pierre-François Pradat
Publikováno v:
Revue Neurologique. 178:S105-S106