Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Thierry Grandmougin"'
Autor:
Jean-Denis Degos, Thierry Grandmougin, Jean-Pascal Lefaucheur, Anne-Catherine Bachoud-Lévi, Catherine Bourdet, Fabrice Lisovoski, Pierre Cesaro, Philippe Hantraye, Marc Peschanski
Publikováno v:
Movement Disorders. 17:1294-1301
Assessment programs recently designed to follow-up patients with Huntington's disease (HD) in therapeutic trials have not included electrophysiological testing in the list of mandatory examinations. This omission is likely due to the current lack of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afdc460a8da5549db7058ab6346f4cc
https://doi.org/10.1002/mds.10273
https://doi.org/10.1002/mds.10273
Autor:
Gianfranco Dalla Barba, Roland Jeny, Jean-Denis Degos, Sophie Baudic, Fabrice Lisovoski, Bassam Haddad, Thierry Grandmougin, Marie-Françoise Boissé, Patrick Maison, Edwige Pailhous, Pierre Brugières, Anne-Marie Ergis, Paolo Bartolomeo, Philippe Hantraye, Catherine Bourdet, Jean-Paul Nǵuyen, Anne-Catherine Bachoud-Lévi, Véronique Gaura, Marc Peschanski, Philippe Remy, Jean-Pascal Lefaucheur, Pierre Cesaro
Publikováno v:
The Lancet. 356:1975-1979
Summary Background Huntington's disease is a neurodegenerative disease of genetic origin that mainly affects the striatum. It has severe motor and cognitive consequences and, up to now, no treatment. Motor and cognitive functions can be restored in e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4b3408f558ac6916d92fed965d9081
https://doi.org/10.1016/s0140-6736(00)03310-9
https://doi.org/10.1016/s0140-6736(00)03310-9
Autor:
Pierre Brugières, Catherine Bourdet, Anne-Marie Ergis, Bassam Haddad, Fabrice Lisovoski, Paolo Bartolomeo, Gianfranco Dalla Barba, Jean-Paul Nguyen, Jean-Denis Degos, P. Hantraye, Roland Jeny, Stéphane Palfi, Gilles-Louis Defer, Philippe Remy, Marc Peschanski, Anne-Catherine Bachoud-Lévi, E Pailhous, Thierry Grandmougin, Pierre Cesaro, Marie-Françoise Boissé, Jean-Pascal Lefaucheur
Publikováno v:
Experimental Neurology. 161:194-202
This study describes issues related to the safety and tolerability of fetal striatal neural allografts as assessed in five patients with Huntington's disease. Huntington's disease (HD) is characterized by motor, cognitive, and behavioral disturbances
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96429d19762d5936efbc144ba4d0ee7
https://doi.org/10.1006/exnr.1999.7239
https://doi.org/10.1006/exnr.1999.7239