Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Alexander de Bruyn"'
Autor:
Alexander de Bruyn, Federica Montagnese, Sonja Holm-Yildiz, Nanna Scharff Poulsen, Tanya Stojkovic, Anthony Behin, Johanna Palmio, Manu Jokela, Jan L De Bleecker, Marianne de Visser, Anneke J van der Kooi, Leroy ten Dam, Cristina Domínguez González, Lorenzo Maggi, Annamaria Gallone, Anna Kostera-Pruszczyk, Anna Macias, Anna Łusakowska, Velina Nedkova, Montse Olive, Rodrigo Álvarez-Velasco, Julia Wanschitz, Carmen Paradas, Fabiola Mavillard, Giorgia Querin, Gorka Fernández-Eulate, Ros Quinlivan, Maggie C Walter, Christophe E Depuydt, Bjarne Udd, John Vissing, Benedikt Schoser, Kristl G Claeys
Publikováno v:
Brain.
Anoctamin-5 related muscle disease is caused by biallelic pathogenic variants in the anoctamin-5 gene (ANO5) and shows variable clinical phenotypes: limb-girdle muscular dystrophy type 12 (LGMD-R12), distal muscular dystrophy type 3 (MMD3), pseudomet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::534560b061be62aae6c0816238239f34
https://doi.org/10.1093/brain/awad088
https://doi.org/10.1093/brain/awad088
Autor:
Patrick Vanderdonckt, Francesca Aloisi, Giancarlo Comi, Alexander de Bruyn, Hans-Peter Hartung, Inge Huitinga, Tanja Kuhlmann, Claudia F. Lucchinetti, Imke Metz, Richard Reynolds, Hans Lassmann
Publikováno v:
Brain communications, 4(2)
Although major progress in multiple sclerosis research has been made during the last decades, key questions related to the cause and the mechanisms of brain and spinal cord pathology remain unresolved. These cover a broad range of topics, including d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16bc2bc51ca72a76faa71c622b71a52d
https://hdl.handle.net/20.500.11755/7abda326-0fb0-478e-8e6d-4ac9508bb0bd
https://hdl.handle.net/20.500.11755/7abda326-0fb0-478e-8e6d-4ac9508bb0bd
Autor:
Thomas Claeys, Philip Van Damme, Kristl G. Claeys, Alexander de Bruyn, Koen Poesen, Xavier Bossuyt, Christophe E. Depuydt, Isaac P Heremans
Publikováno v:
Acta neurologica Belgica. 119(1)
Anti-GQ1b antibodies can be detected in the serum of patients with Miller Fisher syndrome (MFS) and its incomplete forms such as acute ophthalmoparesis (AO), acute ptosis, acute mydriasis, acute oropharyngeal palsy and acute ataxic neuropathy (AAN),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b4692ef1360ee2c00d6a5cc40c79ab3
https://pubmed.ncbi.nlm.nih.gov/30747336
https://pubmed.ncbi.nlm.nih.gov/30747336