Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Borg, Michel"'
Autor:
Fevga, Christina, Tesson, Christelle, Carreras Mascaro, Ana, Courtin, Thomas, Van Coller, Riaan, Sakka, Salma, Ferraro, Federico, Farhat, Nouha, Bardien, Soraya, Damak, Mariem, Carr, Jonathan, Ferrien, Melanie, Boumeester, Valerie, Hundscheid, Jasmijn, Grillenzoni, Nicola, Kessissoglou, Irini A., Kuipers, Demy J.S., Quadri, Marialuisa, Agid, Yves, Anheim, Mathieu, Borg, Michel, Brice, Alexis, Broussolle, Emmanuel, Corvol, Jean Christophe, Damier, Philippe, Defebvre, Luc, Dürr, Alexandra, Durif, Franck, Houeto, Jean Luc, Krack, Paul, Klebe, Stephan, Lesage, Suzanne, Lohmann, Ebba, Martinez, Maria, Mangone, Graziella, Mariani, Louise Laure, Pollak, Pierre, Rascol, Olivier, Tison, François, Tranchant, Christine, Verin, Marc, Viallet, François, Vidailhet, Marie, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Lu, Bedia Marangozog, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouchetara, Sofiane A., Benhassine, Traki, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Romdhan, Sawssan Ben, Mhiri, Chokri, Bouhouche, Ahmed, Bonifati, Vincenzo, Mandemakers, Wim, Kievit, Anneke J.A., Boon, Agnita J.W., Ferreira, Joaquim J., Guedes, Leonor Correia, Hanagasi, Hasmet A., Tufekcioglu, Zeynep, Elibol, Bulent, Dog.u, Okan, Gultekin, Murat, Chien, Hsin F., Barbosa, Egberto, Jardim, Laura Bannach, Rieder, Carlos R.M., Chang, Hsiu Chen, Lu, Chin Song, Wu-Chou, Yah Huei, Yeh, Tu Hsueh, Lopiano, Leonardo, Tassorelli, Cristina, Pacchetti, Claudio, Comi, Cristoforo, Raudino, Francesco, Bertolasi, Laura, Tinazzi, Michele, Bonizzato, Alberto, Ferracci, Carlo, Marconi, Roberto, Guidi, Marco, Onofrj, Marco, Thomas, Astrid, Vanacore, Nicola, Meco, Giuseppe, Fabrizio, Edito, Fabbrini, Giovanni, Berardelli, Alfredo, Stocchi, Fabrizio, Vacca, Laura, Barone, Paolo, Picillo, Marina, De Michele, Giuseppe, Criscuolo, Chiara, De Mari, Michele, Dell'aquila, Claudia, Iliceto, Giovanni, Toni, Vincenzo, Trianni, Giorgio, Saddi, Valeria, Cossu, Gianni, Melis, Maurizio, Hassan, Bassem A., Breedveld, Guido J.
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2022, ⟨10.1093/brain/awac326⟩
Brain, 146(4), 1496-1510. Oxford University Press
Brain-A Journal of Neurology, 2022, ⟨10.1093/brain/awac326⟩
Brain, 146(4), 1496-1510. Oxford University Press
The protein phosphatase 2A complex (PP2A), the major Ser/Thr phosphatase in the brain, is involved in a number of signalling pathways and functions, including the regulation of crucial proteins for neurodegeneration, such as alpha-synuclein, tau and
Autor:
Lanore, Aymeric, Casse, Fanny, Tesson, Christelle, Courtin, Thomas, Menon, Poornima Jayadev, Sambin, Sara, Mangone, Graziella, Mariani, Louise‐Laure, Lesage, Suzanne, Brice, Alexis, Elbaz, Alexis, Corvol, Jean‐Christophe, Agid, Yves, Anheim, Mathieu, Borg, Michel, Broussolle, Emmanuel, Damier, Philippe, Defebvre, Luc, Dürr, Alexandra, Durif, Franck
Publikováno v:
Annals of Neurology; Jul2023, Vol. 94 Issue 1, p123-132, 10p
Autor:
Boot, Erik, Butcher, Nancy J, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M, Udow, Sean, Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M, Marras, Connie, Wood, Nicholas W, Booij, Jan, Lang, Anthony E, Bassett, Anne S, 2DS-associated Parkinson's Disease, International Research Group on 22q11., Tambasco, Nicola, Repetto, Gabriela M, Fritsch, Rosemarie, Tinselboer, Barber M, Vorstman, Jacob As, Mok, Kin Y, Pellene, Luis A, Reich, Stephen G, Schulte, Claudia, Dekker, Annet, Kaneko, Satoshi, Barrett, Matthew J, Prontera, Paolo, Berman, Brian D, Masellis, Mario
Publikováno v:
Neurology
Neurology 90(23), e2059-e2067 (2018). doi:10.1212/WNL.0000000000005660
Neurology 90(23), e2059-e2067 (2018). doi:10.1212/WNL.0000000000005660
OBJECTIVE: To delineate the natural history, diagnosis, and treatment response of Parkinson disease (PD) in individuals with 22q11.2 deletion syndrome (22q11.2DS), and to determine if these patients differ from those with idiopathic PD. METHODS: In t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fcd1a14146eecd9620155355971b5e6f
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Agid, Yves, Anheim, Mathieu, Bonnet, A.-M., Borg, Michel, Brefel-Courbon, Christine, Brice, Alexis, Broussolle, Emmanuel, Corvol, Jean-Christophe, Damier, Philippe, Destée, Alain, Dürr, Alexandra, Durif, Franck, Lesage, Suzanne, Lohmann, Ebba, Martinez, Maria, Pollak, Pierre, Rascol, Olivier, Tison, François, Tranchant, Christine, Vérin, Marc, Viallet, François, Vidailhet, Marie, Tesson, Christelle
Publikováno v:
In The Lancet Neurology December 2018 17(12):1034-1034
Autor:
Payan, Christine A. M., Viallet, François, Agid, Yves, Ludolph, Albert C., Leigh, Peter N., Bensimon, Gilbert, NNIPPS Study Group, Landwehrmeyer, Bernhard Georg, Bonnet, Anne-Marie, Borg, Michel, Durif, Franck, Lacomblez, Lucette, Bloch, Frédéric, Verny, Marc, Fermanian, Jacques
Publikováno v:
PLoS ONE
PLoS ONE, Public Library of Science, 2011, 6 (8), Non spécifié. ⟨10.1371/journal.pone.0022293⟩
PLOS ONE 6(8), e22293 (2011). doi:10.1371/journal.pone.0022293
PLoS ONE, 2011, 6 (8), Non spécifié. ⟨10.1371/journal.pone.0022293⟩
PLoS ONE, Vol 6, Iss 8, p e22293 (2011)
PLoS ONE, Public Library of Science, 2011, 6 (8), Non spécifié. ⟨10.1371/journal.pone.0022293⟩
PLOS ONE 6(8), e22293 (2011). doi:10.1371/journal.pone.0022293
PLoS ONE, 2011, 6 (8), Non spécifié. ⟨10.1371/journal.pone.0022293⟩
PLoS ONE, Vol 6, Iss 8, p e22293 (2011)
PLoS one 6(8), e22293 (2011). doi:10.1371/journal.pone.0022293
Published by PLoS, Lawrence, Kan.
Published by PLoS, Lawrence, Kan.
Autor:
Troiano, André, Elbaz, Alexis, Lohmann, E., Belarbi, S., Vidailhet, Marie, Bonnet, A.-M., Lesage, Suzanne, Pollak, Pierre, Cazeneuve, Cécile, Borg, Michel, Feingold, Josué, Dürr, Alexandra, Tazir, M., Brice, Alexis, Study Group, For The French Parkinson Disease Genetic
Publikováno v:
Neurology, Vol. 75, No 12 (2010) pp. 1118-9
Neurology
Neurology, American Academy of Neurology, 2010, 75 (12), pp.1118-1119. ⟨10.1212/WNL.0b013e3181f39a2e⟩
Neurology, 2010, 75 (12), pp.1118-1119. ⟨10.1212/WNL.0b013e3181f39a2e⟩
Neurology
Neurology, American Academy of Neurology, 2010, 75 (12), pp.1118-1119. ⟨10.1212/WNL.0b013e3181f39a2e⟩
Neurology, 2010, 75 (12), pp.1118-1119. ⟨10.1212/WNL.0b013e3181f39a2e⟩
Currently, mutations in the leucine repeat–rich kinase 2 (LRRK2) gene are the main identifiable genetic cause of Parkinson disease (PD). The Gly2019Ser (G2019S) substitution is the most common mutation and is frequent among North African (40%) and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ea2311f5a8c6c0c4dba929d16c8b803
https://archive-ouverte.unige.ch/unige:32877
https://archive-ouverte.unige.ch/unige:32877
Autor:
Brashear, Allison, Dobyns, William B., Aguiar, Patricia de Carvalho, Borg, Michel, Frijns, C. J. M., Gollamudi, Seema, Green, Andrew, Guimaraes, Joao, Haake, Bret C., Klein, Christine, Linazasoro, Gurutz, Muenchau, Alexander, Raymond, Deborah, Riley, David, Saunders-Pullman, Rachel, Tijssen, Marina A. J., Webb, David, Zaremba, Jacek, Bressman, Susan B., Ozelius, Laurie J.
Publikováno v:
Brain, 130(3), 828-835. Oxford University Press
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset of dystonia and parkinsonism and is caused by mutations in the ATP1A3 gene. We obtained clinical data and sequenced the ATP1A3 gene in 49 subjects from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::fbc68ee71e7a949ebc743504c34b98e2
https://research.rug.nl/en/publications/6605b190-4111-4204-9516-a586ea4225d2
https://research.rug.nl/en/publications/6605b190-4111-4204-9516-a586ea4225d2
Autor:
Romero, Gwendoline, Giordana, Caroline, Launay, Maël, Honnorat, Jérôme, Borg, Michel, Lebrun-Frénay, Christine, Thomas, Pierre
Publikováno v:
In Revue Neurologique March 2017 173 Supplement 2:S179-S179
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.