Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Roy, Anna J."'
Autor:
Batcho, Charles Sèbiyo, Van den Bergh, Peter Y.K., Van Damme, Philip, Roy, Anna J., Thonnard, Jean-Louis, Penta, Massimo *
Publikováno v:
In Neuromuscular Disorders March 2016 26(3):211-220
Autor:
Roy, Anna J, Van den Bergh, Peter, Van Damme, Philip, Doggen, Kris, Van Casteren, Viviane, BNMDR Scientific Committee, the, De Bleecker, Jan, Van Coster, Rudy
Publikováno v:
Acta Neurologica Belgica, Vol. 115, no. 2, p. 97-104 (2014)
Acta Neurologica Belgica
ACTA NEUROLOGICA BELGICA
Acta Neurologica Belgica
ACTA NEUROLOGICA BELGICA
The Belgian Neuromuscular Disease Registry, commissioned in 2008, aims to collect data to improve knowledge on neuromuscular diseases and enhance quality health services for neuromuscular disease patients. This paper presents a clear outline of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e2b3b8e0deef7fb3ca04f4f872a4e5
https://hdl.handle.net/2078.1/157218
https://hdl.handle.net/2078.1/157218
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Koeks, Zaïda, Bladen, Catherine L., Salgado, David, van Zwet, Erik, Pogoryelova, Oksana, McMacken, Grace, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Bellgard, Matthew I., Roy, Anna J., Chamova, Teodora, Guergueltcheva, Velina, Chan, Sophelia, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Wang, Jen, Barišić, Nina, Brabec, Petr, Lähdetie, Jaana, Walter, Maggie C., Schreiber-Katz, Olivia, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Viswanathan, Venkatarman, Bayat, Farhad, Buccella, Filippo, Ferlini, Alessandra, Kimura, En, van den Bergen, Janneke C., Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Kostera-Pruszczyk, Anna, Santos, Rosário, Neagu, Elena, Artemieva, Svetlana, Rasic, Vedrana Milic, Vojinovic, Dina, Posada, Manuel, Bloetzer, Clemens, Klein, Andrea, Díaz-Manera, Jordi, Gallardo, Eduard, Karaduman, A. Ayşe, Oznur, Tunca, Topaloğlu, Haluk, El Sherif, Rasha, Stringer, Angela, Shatillo, Andriy V., Martin, Ann S., Peay, Holly L., Kirschner, Jan, Flanigan, Kevin M., Straub, Volker, Bushby, Kate, Béroud, Christophe, Verschuuren, Jan J., Lochmüller, Hanns
Publikováno v:
Journal of Neuromuscular Diseases; November 2017, Vol. 4 Issue: 4 p293-306, 14p
Autor:
Koeks, Zaïda, Bladen, Catherine L, Salgado, David, Van Zwet, Erik, Pogoryelova, Oksana, McMacken, Grace, Monges, Soledad, Foncuberta, Maria E, Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Bellgard, Matthew I, Roy, Anna J, Chamova, Teodora, Guergueltcheva, Velina, Chan, Sophelia, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Wang, Jen, Barišić, Nina, Brabec, Petr, Lähdetie, Jaana, Walter, Maggie C, Schreiber-Katz, Olivia, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Viswanathan, Venkatarman, Bayat, Farhad, Buccella, Filippo, Ferlini, Alessandra, Kimura, En, Van Den Bergen, Janneke C, Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Kostera-Pruszczyk, Anna, Santos, Rosário, Neagu, Elena, Artemieva, Svetlana, Rasic, Vedrana Milic, Vojinovic, Dina, Posada, Manuel, Blötzer, Clemens, Klein, Andrea, Díaz-Manera, Jordi, Gallardo, Eduard, Karaduman, A Ayşe, Oznur, Tunca, Topaloğlu, Haluk, El Sherif, Rasha, Stringer, Angela, Shatillo, Andriy V, Martin, Ann S, Peay, Holly L, Kirschner, Jan, Flanigan, Kevin M, Straub, Volker, Bushby, Kate, Béroud, Christophe, Verschuuren, Jan J, Lochmüller, Hanns
BACKGROUND Recent short-term clinical trials in patients with Duchenne Muscular Dystrophy (DMD) have indicated greater disease variability in terms of progression than expected. In addition, as average life-expectancy increases, reliable data is requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b4ac1ecfa325c52302eb3eed9daf197
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutations
Autor:
Guergueltcheva, Velina, Chamova, Teodora, Bellgard, Matthew I, Vojinovic, Dina, Straub, Volker, Bloetzer, Clemens, Rasic, Vedrana Milic, Kostera-Pruszczyk, Anna, Dai, Yi, Koeks, Zaïda, El Sherif, Rasha, Neagu, Elena, Dawkins, Hugh, Lamont, Leanne, Campbell, Craig, Walter, Maggie C, Zimowski, Janusz, Santos, Rosário, Korngut, Lawrence, Artemieva, Svetlana, Barišić, Nina, Karaduman, A Ayşe, Kirschner, Jan, Jeannet, Pierre-Yves, Karcagi, Veronika, Roy, Anna J, Peay, Holly L, Lahdetie, Jaana, Van Den Bergen, Janneke C, Díaz-Manera, Jordi, Bayat, Farhad, Kekou, Kyriaki, Chan, Sophelia, Kimura, En, Topaloğlu, Haluk, Joncourt, Franziska, Gallardo, Eduard, Salgado, David, Monges, Soledad, Kosma, Konstantina, Posada, Manuel, Rodrigues, Miriam, Stringer, Angela, Foncuberta, Maria E, Béroud, Christophe, Martin, Ann S, Bushby, Kate, Buccella, Filippo, Aartsma-Rus, Annemieke, Wang, Jen, Schreiber-Katz, Olivia, Roxburgh, Richard, Verschuuren, Jan, Lusakowska, Anna, Garami, Marta, Bladen, Catherine L, Flanigan, Kevin M, Brabec, Petr, Viswanathan, Venkatarman, Shatillo, Andriy V, Lochmüller, Hanns
Analyzing the type and frequency of patient-specific mutations that give rise to Duchenne muscular dystrophy (DMD) is an invaluable tool for diagnostics, basic scientific research, trial planning, and improved clinical care. Locus-specific databases
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e07f74b617c9c10d83be7b9fdfe1f0e