Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Daniel Tanesse"'
Autor:
Florian P. Thomas, Mario A. Saporta, Shahram Attarian, Teresa Sevilla, Rafael Sivera, Gian M. Fabrizi, Filippo Genovese, Amy J. Gray, Simon Bull, Daniel Tanesse, Manuel Rego, Allison Moore, Courtney Hollett, Xavier Paoli, Thomas Sénéchal, Laura Day, Chengyu Ouyang, Samuel Llewellyn, Mark Larkin, Youcef Boutalbi
This study aims to explore the impact of Charcot-Marie-Tooth disease type 1A (CMT1A) and its treatment on patients in European (France, Germany, Italy, Spain, and the United Kingdom) and US real-world practice.Adults with CMT1A (n = 937) were recruit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::657098cba68fda8efd89d3d5bea6fbf1
https://hdl.handle.net/11562/1073227
https://hdl.handle.net/11562/1073227
Autor:
Allison Moore, Manuel Rego, Samuel Llewellyn, Florian P. Thomas, Mark Larkin, Youcef Boutalbi, Xavier Paoli, Shahram Attarian, Gian Maria Fabrizi, Simon Bull, Teresa Sevilla, Rafael Sivera Mascaró, Amy Gray, Courtney Hollett, Filippo Genovese, Mario Saporta, Katia Monteiro, Daniel Tanesse
Background Charcot-Marie-Tooth disease (CMT) is a rare, chronic, progressive motor and sensory neuropathy that affects the peripheral nervous system, leading to progressive, predominantly distal muscle weakness, atrophy, sensory loss and progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20d195cbe08a3e6ec9ef607fb49ff5f0
https://doi.org/10.21203/rs.3.rs-36305/v2
https://doi.org/10.21203/rs.3.rs-36305/v2
Autor:
Amy Gray, Mark Larkin, Gian Maria Fabrizi, Katia Monteiro, Daniel Tanesse, Simon Bull, Teresa Sevilla, Allison Moore, Florian P. Thomas, Filippo Genovese, Youcef Boutalbi, Courtney Hollett, Samuel Llewellyn, Manuel Rego, Rafael Sivera Mascaró, Mario Saporta, Xavier Paoli, Shahram Attarian
Background Charcot-Marie-Tooth disease (CMT) is a rare, chronic, progressive motor and sensory neuropathy that affects the peripheral nervous system, leading to progressive, predominantly distal muscle weakness, atrophy, sensory loss and progressive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48469872daa5348843d5a2e001187d4a
https://doi.org/10.21203/rs.3.rs-36305/v1
https://doi.org/10.21203/rs.3.rs-36305/v1
Autor:
Jean-Yves Hogrel, Daniel Tanesse, Laurence Attolini, Eric Azabou, Tanya Stojkovic, Rafaëlle Bernard, Odile Dubourg, Marie-Noëlle Lefebvre, Michel Fontes, Mahmoud Al-Moussawi, Shahram Attarian, Olivier Blin, Elisabeth Jouve, Pierre-Marie Gonnaud, Jean Pouget, Francois Vacherot, Jean-Francois Remec, Sadek Yaici, Joëlle Micallef, Severine Pitel, Laurent Jomir
Publikováno v:
The Lancet Neurology. 8:1103-1110
Summary Background Charcot–Marie–Tooth disease type 1A (CMT1A) is a hereditary peripheral neuropathy that affects roughly one in 5000 births. No specific therapy currently exists for this degenerative disorder, which is characterised by distal pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::192f9b483a6b5c3ee67c715c170b6b39
https://doi.org/10.1016/s1474-4422(09)70260-1
https://doi.org/10.1016/s1474-4422(09)70260-1
