Early-onset phenotype in a patient with an intermediate allele and a large SCA1 expansion: a case report von Baille, Guillaume, Geoffre, Nicolas, Wissocq, Anna, Planté-Bordeneuve, Pauline, Mutez, Eugénie, Huin, Vincent

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Doses of Botulinum Toxin in Cervical Dystonia: Does Ultrasound Guidance Change Injection Practices? von Kreisler, Alexandre, Mortain, Léa, Watel, Kaëlig, Mutez, Eugénie, Defebvre, Luc, Duhamel, Alain

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Cognitive Impairment Is Part of the Phenotype of Cerebellar Ataxia, Neuropathy, Vestibular Areflexia Syndrome (CANVAS) von Dujardin, Kathy, Tard, Céline, Diglé, Emily, Herlin, Virginie, Mutez, Eugénie, Davion, Jean‐Baptiste, Wissocq, Anna, Delforge, Violette, Kuchcinski, Gregory, Huin, Vincent

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Reply to: “Further Evidence of Cerebellar Cognitive Affective/Schmahmann Syndrome in RFC1‐Related Syndrome” von Dujardin, Kathy, Tard, Céline, Diglé, Emily, Herlin, Virginie, Mutez, Eugénie, Davion, Jean‐Baptiste, Wissocq, Anna, Delforge, Violette, Kuchcinski, Gregory, Huin, Vincent

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Centrosomal cohesion deficits as cellular biomarker in lymphoblastoid cell lines from LRRK2 Parkinson's disease patients von Fernández, Belén, Lara Ordóñez, Antonio Jesús, Fdez, Elena, Mutez, Eugénie, Comptdaer, Thomas, Leghay, Coline, Kreisler, Alexandre, Simonin, Clémence, Vandewynckel, Laurine, Defebvre, Luc, Destée, Alain, Bleuse, Séverine, Taymans, Jean-Marc, Chartier-Harlin, Marie-Christine, Hilfiker, Sabine

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Involvement of the immune system, endocytosis and EIF2 signaling in both genetically determined and sporadic forms of Parkinson's disease von Mutez, Eugénie, Nkiliza, Aurore, Belarbi, Karim, de Broucker, Amélie, Vanbesien-Mailliot, Christel, Bleuse, Séverine, Duflot, Aurélie, Comptdaer, Thomas, Semaille, Pierre, Blervaque, Renaud, Hot, David, Leprêtre, Frederic, Figeac, Martin, Destée, Alain, Chartier-Harlin, Marie-Christine

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Transcriptomic signatures of brain regional vulnerability to Parkinson’s disease von Keo, Arlin, Mahfouz, Ahmed, Ingrassia, Angela M. T., Meneboo, Jean-Pascal, Villenet, Celine, Mutez, Eugénie, Comptdaer, Thomas, Lelieveldt, Boudewijn P. F., Figeac, Martin, Chartier-Harlin, Marie-Christine, van de Berg, Wilma D. J., van Hilten, Jacobus J., Reinders, Marcel J. T.

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Functional Analyses of Two Novel LRRK2 Pathogenic Variants in Familial Parkinson′s Disease von Coku, Ilda, Mutez, Eugénie, Eddarkaoui, Sabiha, Carrier, Sébastien, Marchand, Antoine, Deldycke, Claire, Goveas, Liesel, Baille, Guillaume, Tir, Mélissa, Magnez, Romain, Thuru, Xavier, Vermeersch, Gaëlle, Vandenberghe, Wim, Buée, Luc, Defebvre, Luc, Sablonnière, Bernard, Chartier‐Harlin, Marie‐Christine, Taymans, Jean‐Marc, Huin, Vincent

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A randomized, controlled, double-blind, crossover trial of zonisamide in myoclonus-dystonia von Hainque, Elodie, Vidailhet, Marie, Cozic, Nathalie, Charbonnier-Beaupel, Fanny, Thobois, Stéphane, Tranchant, Christine, Brochard, Vanessa, Glibert, Gérald, Drapier, Sophie, Mutez, Eugénie, Doe De Maindreville, Anne, Lebouvier, Thibaud, Hubsch, Cécile, Degos, Bertrand, Bonnet, Cécilia, Grabli, David, Legrand, André-Pierre, Méneret, Aurélie, Azulay, Jean-Philippe, Bissery, Anne, Zahr, Noël, Clot, Fabienne, Mallet, Alain, Dupont, Sophie, Apartis, Emmanuelle, Corvol, Jean-Christophe, Roze, Emmanuel

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Mind the Gap: LRRK2 Phenotypes in the Clinic vs. in Patient Cells von Goveas, Liesel, Mutez, Eugénie, Chartier-Harlin, Marie-Christine, Taymans, Jean-Marc

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RNA-binding disturbances as a continuum from spinocerebellar ataxia type 2 to Parkinson disease von Nkiliza, Aurore, Mutez, Eugénie, Simonin, Clémence, Leprêtre, Frédéric, Duflot, Aurélie, Figeac, Martin, Villenet, Céline, Semaille, Pierre, Comptdaer, Thomas, Genet, Alexandre, Sablonnière, Bernard, Devos, David, Defebvre, Luc, Destée, Alain, Chartier-Harlin, Marie-Christine

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Alterations in the LRRK2-Rab pathway in urinary extracellular vesicles as Parkinson’s disease and pharmacodynamic biomarkers von 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

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Mini-Exome Coupled to Read-Depth Based Copy Number Variation Analysis in Patients with Inherited Ataxias von Marelli, Cecilia, Guissart, Claire, Hubsch, Cecile, Renaud, Mathilde, Villemin, Jean-Philippe, Larrieu, Lise, Charles, Perrine, Ayrignac, Xavier, Sacconi, Sabrina, Collignon, Patrick, Cuntz-Shadfar, Danielle, Perrin, Laurine, Benarrosh, Anelia, Degardin, Adrian, Lagha-Boukbiza, Ouhaïd, Mutez, Eugenie, Carlander, Bertrand, Morales, Raul Juntas, Gonzalez, Victoria, Carra-Dalliere, Clarisse, Azakri, Souhayla, Mignard, Claude, Ollagnon, Elisabeth, Pageot, Nicolas, Chretien, Dominique, Geny, Christian, Azulay, Jean-Philippe, Tranchant, Christine, Claustres, Mireille, Labauge, Pierre, Anheim, Mathieu, Goizet, Cyril, Calvas, Patrick, Koenig, Michel

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Transcriptional profile of Parkinson blood mononuclear cells with LRRK2 mutation von Mutez, Eugénie, Larvor, Lydie, Leprêtre, Frédéric, Mouroux, Vincent, Hamalek, Dorota, Kerckaert, Jean-Pierre, Pérez-Tur, Jordi, Waucquier, Nawal, Vanbesien-Mailliot, Christel, Duflot, Aurélie, Devos, David, Defebvre, Luc, Kreisler, Alexandre, Frigard, Bernard, Destée, Alain, Chartier-Harlin, Marie-Christine

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Lipid-lowering drugs are associated with delayed onset and slower course of Parkinson's disease von Mutez, Eugénie, Duhamel, Alain, Defebvre, Luc, Bordet, Régis, Destée, Alain, Kreisler, Alexandre

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SNCA locus duplication carriers: from genetics to Parkinson disease phenotypes von Mutez, Eugénie, Leprêtre, Frédéric, Le Rhun, Emilie, Larvor, Lydie, Duflot, Aurélie, Mouroux, Vincent, Kerckaert, Jean-Pierre, Figeac, Martin, Dujardin, Kathy, Destée, Alain, Chartier-Harlin, Marie-Christine

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Protein phosphatase 2A holoenzymes regulate leucine-rich repeat kinase 2 phosphorylation and accumulation von Drouyer, Matthieu, Bolliger, Marc F., Lobbestael, Evy, Van den Haute, Chris, Emanuele, Marco, Lefebvre, Réginald, Sibran, William, De Wit, Tina, Leghay, Coline, Mutez, Eugénie, Dzamko, Nicolas, Halliday, Glenda M., Murayama, Shigeo, Martoriati, Alain, Cailliau, Katia, Bodart, Jean-François, Chartier-Harlin, Marie-Christine, Baekelandt, Veerle, Nichols, R. Jeremy, Taymans, Jean-Marc

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Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2 von Boot, Erik, Butcher, Nancy J, Udow, Sean, Marras, Connie, Mok, Kin Y, Kaneko, Satoshi, Barrett, Matthew J, Prontera, Paolo, Berman, Brian D, Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M, Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M, Wood, Nicholas W, Booij, Jan, Lang, Anthony E, Bassett, Anne S

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Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice von Cuvelier, Elodie, Méquinion, Mathieu, Leghay, Coline, Sibran, William, Stievenard, Aliçia, Sarchione, Alessia, Bonte, Marie-Amandine, Vanbesien-Mailliot, Christel, Viltart, Odile, Saitoski, Kevin, Caron, Emilie, Labarthe, Alexandra, Comptdaer, Thomas, Semaille, Pierre, Carrié, Hélène, Mutez, Eugénie, Gressier, Bernard, Destée, Alain, Chartier-Harlin, Marie-Christine, Belarbi, Karim

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Anatomy‐guided injections of botulinum neurotoxin in neck muscles: how accurate is needle placement? von Kreisler, A., Simonin, C., Degardin, A., Mutez, E., Defebvre, L.

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