NADPH oxidases in Parkinson’s disease: a systematic review

di Belarbi, Karim, Cuvelier, Elodie, Destée, Alain, Gressier, Bernard, Chartier-Harlin, Marie-Christine
Pubblicato in Mol Neurodegener (2017)

Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation

di Devos, David, Tchofo, P. Jissendi, Vuillaume, Isabelle, Destée, Alain, Batey, Stephanie, Burn, John, Chinnery, Patrick F.
Pubblicazione 2009

Role of Basal Ganglia Circuits in Resisting Interference by Distracters: A swLORETA Study

di Bocquillon, Perrine, Bourriez, Jean-Louis, Palmero-Soler, Ernesto, Destée, Alain, Defebvre, Luc, Derambure, Philippe, Dujardin, Kathy
Pubblicazione 2012

Unusual MR Findings of the Brain Stem in Arterial Hypertension

di de Seze, Jérôme, Mastain, Bruno, Stojkovic, Tanya, Ferriby, Didier, Pruvo, Jean Pierre, Destée, Alain, Vermersch, Patrick
Pubblicato in AJNR Am J Neuroradiol (2000)

Xenopus laevis as a Model to Identify Translation Impairment

di de Broucker, Amélie, Semaille, Pierre, Cailliau, Katia, Martoriati, Alain, Comptdaer, Thomas, Bodart, Jean-François, Destée, Alain, Chartier-Harlin, Marie-Christine
Pubblicato in J Vis Exp (2015)

Multiclass classification of FDG PET scans for the distinction between Parkinson's disease and atypical parkinsonian syndromes()()

di Garraux, Gaëtan, Phillips, Christophe, Schrouff, Jessica, Kreisler, Alexandre, Lemaire, Christian, Degueldre, Christian, Delcour, Christian, Hustinx, Roland, Luxen, André, Destée, Alain, Salmon, Eric
Pubblicazione 2013

Memantine for axial signs in Parkinson's disease: a randomised, double-blind, placebo-controlled pilot study

di Moreau, Caroline, Delval, Arnaud, Tiffreau, Vincent, Defebvre, Luc, Dujardin, Kathy, Duhamel, Alain, Petyt, Gregory, Hossein-Foucher, Claude, Blum, David, Sablonnière, Bernard, Schraen, Susanna, Allorge, Delphine, Destée, Alain, Bordet, Régis, Devos, David
Pubblicazione 2013

Centrosomal cohesion deficits as cellular biomarker in lymphoblastoid cell lines from LRRK2 Parkinson's disease patients

di 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
Pubblicato in Biochem J (2019)

External globus pallidus stimulation modulates brain connectivity in Huntington's disease

di Ligot, Noémie, Krystkowiak, Pierre, Simonin, Clémence, Goldman, Serge, Peigneux, Philippe, Van Naemen, John, Monclus, Michel, Lacroix, Simon Frédéric, Devos, David, Dujardin, Kathy, Delmaire, Christine, Bardinet, Eric, Delval, Arnaud, Delliaux, Marie, Defebvre, Luc, Yelnik, Jerome, Blond, Serge, Destée, Alain, De Tiège, Xavier
Pubblicazione 2011

Overexpression of Wild-Type Human Alpha-Synuclein Causes Metabolism Abnormalities in Thy1-aSYN Transgenic Mice

di 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
Pubblicato in Front Mol Neurosci (2018)

Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy

di Klebe, Stephan, Depienne, Christel, Gerber, Sylvie, Challe, Georges, Anheim, Mathieu, Charles, Perrine, Fedirko, Estelle, Lejeune, Elodie, Cottineau, Julien, Brusco, Alfredo, Dollfus, Hélène, Chinnery, Patrick F., Mancini, Cecilia, Ferrer, Xavier, Sole, Guilhem, Destée, Alain, Mayer, Jean-Michel, Fontaine, Bertrand, de Seze, Jérôme, Clanet, Michel, Ollagnon, Elisabeth, Busson, Philippe, Cazeneuve, Cécile, Stevanin, Giovanni, Kaplan, Josseline, Rozet, Jean-Michel, Brice, Alexis, Durr, Alexandra
Pubblicazione 2012

Targeting Chelatable Iron as a Therapeutic Modality in Parkinson's Disease

di Devos, David, Moreau, Caroline, Devedjian, Jean Christophe, Kluza, Jérome, Petrault, Maud, Laloux, Charlotte, Jonneaux, Aurélie, Ryckewaert, Gilles, Garçon, Guillaume, Rouaix, Nathalie, Duhamel, Alain, Jissendi, Patrice, Dujardin, Kathy, Auger, Florent, Ravasi, Laura, Hopes, Lucie, Grolez, Guillaume, Firdaus, Wance, Sablonnière, Bernard, Strubi-Vuillaume, Isabelle, Zahr, Noel, Destée, Alain, Corvol, Jean-Christophe, Pöltl, Dominik, Leist, Marcel, Rose, Christian, Defebvre, Luc, Marchetti, Philippe, Cabantchik, Z. Ioav, Bordet, Régis
Pubblicazione 2014

Polymorphism of the dopamine transporter type 1 gene modifies the treatment response in Parkinson’s disease

di Moreau, Caroline, Meguig, Sayah, Corvol, Jean-Christophe, Labreuche, Julien, Vasseur, Francis, Duhamel, Alain, Delval, Arnaud, Bardyn, Thomas, Devedjian, Jean-Christophe, Rouaix, Nathalie, Petyt, Gregory, Brefel-Courbon, Christine, Ory-Magne, Fabienne, Guehl, Dominique, Eusebio, Alexandre, Fraix, Valérie, Saulnier, Pierre-Jean, Lagha-Boukbiza, Ouhaid, Durif, Frank, Faighel, Mirela, Giordana, Caroline, Drapier, Sophie, Maltête, David, Tranchant, Christine, Houeto, Jean-Luc, Debû, Bettina, Azulay, Jean-Philippe, Tison, François, Destée, Alain, Vidailhet, Marie, Rascol, Olivier, Dujardin, Kathy, Defebvre, Luc, Bordet, Régis, Sablonnière, Bernard, Devos, David
Pubblicato in Brain (2015)

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

di Lesage, Suzanne, Drouet, Valérie, Majounie, Elisa, Deramecourt, Vincent, Jacoupy, Maxime, Nicolas, Aude, Cormier-Dequaire, Florence, Hassoun, Sidi Mohamed, Pujol, Claire, Ciura, Sorana, Erpapazoglou, Zoi, Usenko, Tatiana, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Ding, Jinhui, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Vidailhet, Marie, Corvol, Jean-Christophe, Krack, Paul, Leutenegger, Anne-Louise, Nalls, Michael A., Hernandez, Dena G., Heutink, Peter, Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Gasser, Thomas, Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Kabashi, Edor, Singleton, Andrew, Corti, Olga, Brice, Alexis
Pubblicato in Am J Hum Genet (2016)

Independent and joint effects of the MAPT and SNCA genes in Parkinson's disease

di Elbaz, Alexis, Ross, Owen A., Ioannidis, John P.A., Soto-Ortolaza, Alexandra I, Moisan, Frédéric, Aasly, Jan, Annesi, Grazia, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Gibson, J. Mark, Gispert, Suzana, Hadjigeorgiou, Georgios M., Jasinska-Myga, Barbara, Klein, Christine, Krüger, Rejko, Lambert, Jean-Charles, Lohmann, Katja, van de Loo, Simone, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugénie, Nilsson, Christer, Opala, Grzegorz, Puschmann, Andreas, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Stefanis, Leonidas, Uitti, Ryan J., Valente, Enza Maria, Vilariño-Güell, Carles, Wirdefeldt, Karin, Wszolek, Zbigniew K., Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J.
Pubblicazione 2011

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

di Chartier-Harlin, Marie-Christine, Dachsel, Justus C., Vilariño-Güell, Carles, Lincoln, Sarah J., Leprêtre, Frédéric, Hulihan, Mary M., Kachergus, Jennifer, Milnerwood, Austen J., Tapia, Lucia, Song, Mee-Sook, Le Rhun, Emilie, Mutez, Eugénie, Larvor, Lydie, Duflot, Aurélie, Vanbesien-Mailliot, Christel, Kreisler, Alexandre, Ross, Owen A., Nishioka, Kenya, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Melrose, Heather L., Behrouz, Bahareh, Keeling, Brett H., Bacon, Justin A., Hentati, Emna, Williams, Lindsey, Yanagiya, Akiko, Sonenberg, Nahum, Lockhart, Paul J., Zubair, Abba C., Uitti, Ryan J., Aasly, Jan O., Krygowska-Wajs, Anna, Opala, Grzegorz, Wszolek, Zbigniew K., Frigerio, Roberta, Maraganore, Demetrius M., Gosal, David, Lynch, Tim, Hutchinson, Michael, Bentivoglio, Anna Rita, Valente, Enza Maria, Nichols, William C., Pankratz, Nathan, Foroud, Tatiana, Gibson, Rachel A., Hentati, Faycal, Dickson, Dennis W., Destée, Alain, Farrer, Matthew J.
Pubblicazione 2011

The protective effect of LRRK2 p.R1398H on risk of Parkinson’s disease is independent of MAPT and SNCA variants

di Heckman, Michael G., Elbaz, Alexis, Soto-Ortolaza, Alexandra I., Serie, Daniel J., Aasly, Jan O., Annesi, Grazia, Auburger, Georg, Bacon, Justin A., Boczarska-Jedynak, Magdalena, Bozi, Maria, Brighina, Laura, Chartier-Harlin, Marie-Christine, Dardiotis, Efthimios, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Fiske, Brian, Gispert, Suzana, Hadjigeorgiou, Georgios M., Hattori, Nobutaka, Ioannidis, John P. A., Jasinska-Myga, Barbara, Jeon, Beom S., Kim, Yun Joong, Klein, Christine, Kruger, Rejko, Kyratzi, Elli, Lin, Chin-Hsien, Lohmann, Katja, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D., Mutez, Eugénie, Opala, Grzegorz, Park, Sung Sup, Petrucci, Simona, Quattrone, Aldo, Sharma, Manu, Silburn, Peter A., Sohn, Young Ho, Stefanis, Leonidas, Tadic, Vera, Tomiyama, Hiroyuki, Uitti, Ryan J., Valente, Enza Maria, Vassilatis, Demetrios K., Vilariño-Güell, Carles, White, Linda R., Wirdefeldt, Karin, Wszolek, Zbigniew K., Wu, Ruey-Meei, Xiromerisiou, Georgia, Maraganore, Demetrius M., Farrer, Matthew J., Ross, Owen A.
Pubblicazione 2013