Zobrazeno 1 - 10
of 120
pro vyhledávání: '"A. Mejat"'
Autor:
Gusset, Nicole, Stalens, Caroline, Stumpe, Eva, Klouvi, Lori, Mejat, Alexandre, Ouillade, Marie-Christine, de Lemus, Mencía
Publikováno v:
In Neuromuscular Disorders May 2021 31(5):419-430
Autor:
Anna Ambrosini, Ros Quinlivan, Valeria A. Sansone, Ingeborg Meijer, Guus Schrijvers, Aad Tibben, George Padberg, Maarten de Wit, Ellen Sterrenburg, Alexandre Mejat, Alexandra Breukel, Michal Rataj, Hanns Lochmüller, Raffaella Willmann, on behalf of the 235th ENMC workshop study group
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract Background Patient and public involvement for co-creation is increasingly recognized as a valuable strategy to develop healthcare research targeting patients’ real needs. However, its practical implementation is not as advanced and unanimo
Externí odkaz:
https://doaj.org/article/9a328ce2a35d47f09c3c4bc026f358dc
Autor:
Adrien Moreau, Jean‐Baptiste Reisqs, Helene Delanoe‐Ayari, Marion Pierre, Alexandre Janin, Antoine Deliniere, Francis Bessière, Albano C. Meli, Azzouz Charrabi, Estele Lafont, Camille Valla, Delphine Bauer, Elodie Morel, Vincent Gache, Gilles Millat, Xavier Nissan, Adele Faucherre, Chris Jopling, Sylvain Richard, Alexandre Mejat, Philippe Chevalier
Publikováno v:
Clinical and Translational Medicine, Vol 11, Iss 3, Pp n/a-n/a (2021)
Abstract Background Severe ventricular rhythm disturbances are the hallmark of arrhythmogenic cardiomyopathy (ACM), and are often explained by structural conduction abnormalities. However, comprehensive investigations of ACM cell electrical instabili
Externí odkaz:
https://doaj.org/article/c9664adcb3fe4088aa3cbb1ca8360b5b
Autor:
Borut Peterlin, Francesca Gualandi, Ales Maver, Serenella Servidei, Silvère M van der Maarel, Francoise Lamy, Alexander Mejat, Teresinha Evangelista, Alessandra Ferlini
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0239329 (2020)
The genetic diagnostics of inherited neuromuscular diseases (NMDs) is challenging due to their clinical and genetic heterogeneity. We launched an online survey within the EURO-NMD European Reference Network (ERN) to collect information about the avai
Externí odkaz:
https://doaj.org/article/7319d679acbe4b5f808ec0d9ffd0df57
Autor:
Doñate Puertas, R., Meugnier, E., Romestaing, C., Rey, C., Morel, E., Lachuer, J., Gadot, N., Scridon, A., Julien, C., Tronc, F., Chapuis, B., Valla, C., Janin, A., Pirola, L., Méjat, A., Rome, S., Chevalier, Philippe
Publikováno v:
In Translational Research June 2017 184:57-67
Autor:
Federica Montagnese, Katy de Valle, Richard J.L.F. Lemmers, Karlien Mul, Julie Dumonceaux, Nicol Voermans, Giorgio Tasca, Maria Gomez-Rodulfo, Sabrina Sacconi, Richard Lemmers, Pilar Camano, Emiliano Giardina, Nienke van der Stoep, Sarah Burton-Jones, Frederique Magdinier, Valerie Race, Sheila Hawkins, Alexandre Mejat, Piraye Oflazer, Lorenzo Guizzaro, Jamshid Arjomand, Yann Pereon, Giulia Ricci, Enrico Bugiardini, Alexandra Belayew
Publikováno v:
Neuromuscular Disorders, 33, 447-462
Neuromuscular Disorders, 33, 5, pp. 447-462
Neuromuscular Disorders, 33, 5, pp. 447-462
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09115dcaa4a5413949563d5406e1316e
http://hdl.handle.net/2066/293214
http://hdl.handle.net/2066/293214
Autor:
Breukel, Alexandra, Willmann, Raffaella, Adcock, Kate, Méjat, Alexandre, Meijer, Ingeborg, Ferreiro, Ana
Publikováno v:
In Neuromuscular Disorders March 2023 33(3):285-287
Autor:
N.C. Voermans, M. Vriens-Munoz Bravo, G.W. Padberg, P. Laforêt, N. van Alfen, S. Attarian, U.A. Badrising, E. Bugiardini, P. Camano González, R.Y. Carlier, I. Desguerre, J. Diaz-Manera, J. Dumonceaux, B.G. van Engelen, T. Evangelista, S. Khosla, A. López de Munain, S.M. van der Maarel, A. Mejat, M. Monforte, F. Montagnese, K. Mul, P. Oflazer, B. Porter, S. Quijano-Roy, E. Ricci, S. Sacconi, V.A. Sansone, B. Schoser, J. Statland, E. Stumpe, G. Tasca, R. Tawil, C. Turner, J. Vissing
Publikováno v:
Neuromuscular Disorders, 31, 907-918
Neuromuscular Disorders, 31, 9, pp. 907-918
Neuromuscular Disorders, 31, 9, pp. 907-918
Item does not contain fulltext
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf1c5a1ec31a3584b8c54220e6014cec
https://doi.org/10.1016/j.nmd.2021.07.013
https://doi.org/10.1016/j.nmd.2021.07.013
Autor:
Compagnat, F., Chalmendrier, C., Méjat, E., Rebrab, R., Nétillard, C., Martin, G., Tissot, E.
Publikováno v:
In Le Pharmacien Hospitalier et Clinicien March 2013 48(1):4-11
Autor:
Méjat, Alexandre, Decostre, Valérie, Li, Juan, Renou, Laure, Kesari, Akanchha, Hantaï, Daniel, Stewart, Colin L., Xiao, Xiao, Hoffman, Eric, Bonne, Gisèle, Misteli, Tom
Publikováno v:
The Journal of Cell Biology, 2009 Jan 01. 184(1), 31-44.
Externí odkaz:
https://www.jstor.org/stable/20537115