Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sarchione, Alessia"'
Autor:
Marchand, Antoine1 (AUTHOR) antoine.marchand@inserm.fr, Sarchione, Alessia1 (AUTHOR) alessia.sarchione@inserm.fr, Athanasopoulos, Panagiotis S.2 (AUTHOR) athanasopoulospanag@hotmail.com, Roy, Hélène Bauderlique-Le3 (AUTHOR) helene.bauderlique@ibl.cnrs.fr, Goveas, Liesel1 (AUTHOR) liesel-mary.goveas@inserm.fr, Magnez, Romain4 (AUTHOR) romain.magnez@inserm.fr, Drouyer, Matthieu1 (AUTHOR) mdrouyer@cmri.org.au, Emanuele, Marco1 (AUTHOR) memanuele@icloud.com, Ho, Franz Y.2 (AUTHOR) y.f.ho@rug.nl, Liberelle, Maxime1 (AUTHOR) maxime.liberelle@inserm.fr, Melnyk, Patricia1 (AUTHOR) patricia.melnyk@univ-lille.fr, Lebègue, Nicolas1 (AUTHOR) nicolas.lebegue@univ-lille.fr, Thuru, Xavier4 (AUTHOR) xavier.thuru@inserm.fr, Nichols, R. Jeremy5 (AUTHOR) rjnichols@stanford.edu, Greggio, Elisa6 (AUTHOR) elisa.greggio@unipd.it, Kortholt, Arjan2 (AUTHOR) a.kortholt@rug.nl, Galli, Thierry7,8 (AUTHOR) thierry.galli@inserm.fr, Chartier-Harlin, Marie-Christine1 (AUTHOR) marie-christine.chartier-harlin@inserm.fr, Taymans, Jean-Marc1 (AUTHOR) marie-christine.chartier-harlin@inserm.fr
Publikováno v:
Cells (2073-4409). Mar2022, Vol. 11 Issue 6, p1018. 19p.
Autor:
Taymans, Jean-Marc, Mutez, Eugénie, Sibran, William, Vandewynckel, Laurine, Deldycke, Claire, Bleuse, Séverine, Marchand, Antoine, Sarchione, Alessia, Leghay, Coline, Kreisler, Alexandre, Simonin, Clémence, Koprich, James, Baille, Guillaume, Defebvre, Luc, Dujardin, Kathy, Destée, Alain, Chartier-Harlin, Marie-Christine
Publikováno v:
NPJ Parkinson's Disease; Dec2023, Vol. 9 Issue 1, p1-14, 14p
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Marchand, Antoine, Drouyer, Matthieu, Sarchione, Alessia, Chartier-Harlin, Marie-Christine, Taymans, Jean-Marc
Publikováno v:
Frontiers in Neuroscience
Mutations in the Leucine Rich Repeat Kinase 2 (LRRK2) gene are linked to autosomal dominant Parkinson's disease (PD), and genetic variations at the LRRK2 locus are associated with an increased risk for sporadic PD. This gene encodes a kinase that is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::dbdeea1d5cd7d57079ada17b6be894c2
http://europepmc.org/articles/PMC7308437
http://europepmc.org/articles/PMC7308437
Autor:
Cuvelier, Elodie, Mequinion, Mathieu, Leghay, Coline, Sibran, William, Stievenard, Alicia, Sarchione, Alessia, Bonte, Marie-Amandine, Vanbesien, Christel, Viltart, Odile, Saitoski, Kevin, Caron, Emilie, Labarthe, Alexandra, Comptdaer, Thomas, Semaille, Pierre, Carrie, Helene, Mutez, Eugenie, Gressier, Bernard, Destée, Alain, Chartier Harlin, Marie-Christine, Belarbi, Karim-Ali
Publikováno v:
Frontiers in Molecular Neuroscience
Frontiers in Molecular Neuroscience, 2018, 11, pp.321. ⟨10.3389/fnmol.2018.00321⟩
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Frontiers in Molecular Neuroscience, Frontiers Media, 2018, 11, pp.321. ⟨10.3389/fnmol.2018.00321⟩
Frontiers in Molecular Neuroscience, 2018, 11, pp.321. ⟨10.3389/fnmol.2018.00321⟩
Frontiers in Molecular Neuroscience, Vol 11 (2018)
Frontiers in Molecular Neuroscience, Frontiers Media, 2018, 11, pp.321. ⟨10.3389/fnmol.2018.00321⟩
International audience; Parkinson's disease is a progressive neurodegenerative disorder characterized by loss of dopaminergic neurons, pathological accumulation of alpha-synuclein and motor symptoms, but also by non-motor symptoms. Metabolic abnormal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::80ebd3d5c0abff5eaf1eca5280d7d8e6
https://hal.univ-lille.fr/hal-03261246
https://hal.univ-lille.fr/hal-03261246
