Torthaí cuardaigh - Anheim, Mathieu

Joint Consultation by a Neurogeneticist of Movement Disorders and a Psychodynamic Psychotherapist: An Occasion for Subjectivization de réir Putois, Olivier, Bacqué, Marie-Frédérique, Anheim, Mathieu

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Cerebral vasculitis of medium-sized vessels as a possible mechanism of brain damage in COVID-19 patients de réir Lersy, François, Anheim, Mathieu, Willaume, Thibault, Chammas, Agathe, Brisset, Jean-Christophe, Cotton, François, Kremer, Stéphane

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3 de réir Renaud, Mathilde, Marcel, Christophe, Rudolf, Gabrielle, Schaeffer, Mickaël, Lagha-Boukbiza, Ouhaïd, Chanson, Jean-Baptiste, Chelly, Jamel, Anheim, Mathieu, Tranchant, Christine

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia de réir Wirth, Thomas, Méneret, Aurélie, Drouot, Nathalie, Rudolf, Gabrielle, Lagha Boukbiza, Ouhaid, Chelly, Jamel, Tranchant, Christine, Piton, Amélie, Roze, Emmanuel, Anheim, Mathieu

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Critical illness-associated cerebral microbleeds for patients with severe COVID-19: etiologic hypotheses de réir Lersy, François, Willaume, Thibault, Brisset, Jean-Christophe, Collange, Olivier, Helms, Julie, Schneider, Francis, Chammas, Agathe, Willaume, Alexandre, Meyer, Nicolas, Anheim, Mathieu, Cotton, François, Kremer, Stéphane

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Neurologic Features in Severe SARS-CoV-2 Infection de réir Helms, Julie, Kremer, Stéphane, Merdji, Hamid, Clere-Jehl, Raphaël, Schenck, Malika, Kummerlen, Christine, Collange, Olivier, Boulay, Clotilde, Fafi-Kremer, Samira, Ohana, Mickaël, Anheim, Mathieu, Meziani, Ferhat

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2) de réir Guissart, Claire, Drouot, Nathalie, Oncel, Ibrahim, Leheup, Bruno, Gershoni-Barush, Ruth, Muller, Jean, Ferdinandusse, Sacha, Larrieu, Lise, Anheim, Mathieu, Arslan, Elif Acar, Claustres, Mireille, Tranchant, Christine, Topaloglu, Haluk, Koenig, Michel

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders de réir Montaut, Solveig, Tranchant, Christine, Drouot, Nathalie, Rudolf, Gabrielle, Guissart, Claire, Tarabeux, Julien, Stemmelen, Tristan, Velt, Amandine, Fourrage, Cécile, Nitschké, Patrick, Gerard, Bénédicte, Mandel, Jean-Louis, Koenig, Michel, Chelly, Jamel, Anheim, Mathieu

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Sleep in ADCY5-Related Dyskinesia: Prolonged Awakenings Caused by Abnormal Movements de réir Méneret, Aurélie, Roze, Emmanuel, Maranci, Jean-Baptiste, Dodet, Pauline, Doummar, Diane, Riant, Florence, Tranchant, Christine, Fraix, Valérie, Anheim, Mathieu, Ekmen, Asya, McGovern, Eavan, Vidailhet, Marie, Arnulf, Isabelle, Leu-Semenescu, Smaranda

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Emerging topics in FXTAS de réir Hall, Deborah A, Birch, Rachael C, Anheim, Mathieu, Jønch, Aia E, Pintado, Elizabeth, O’Keefe, Joanne, Trollor, Julian N, Stebbins, Glenn T, Hagerman, Randi J, Fahn, Stanley, Berry-Kravis, Elizabeth, Leehey, Maureen A

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Health-Related Quality of Life Is Severely Affected in Primary Orthostatic Tremor de réir Maugest, Lucie, McGovern, Eavan M., Mazalovic, Katia, Doulazmi, Mohamed, Apartis, Emmanuelle, Anheim, Mathieu, Bourdain, Frédéric, Benchetrit, Eve, Czernecki, Virginie, Broussolle, Emmanuel, Bonnet, Cecilia, Falissard, Bruno, Jahanshahi, Marjan, Vidailhet, Marie, Roze, Emmanuel

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Erratum: Emerging topics in FXTAS de réir Hall, Deborah A, Birch, Rachael C, Anheim, Mathieu, Jønch, Aia E, Pintado, Elizabeth, O’Keefe, Joan A, Trollor, Julian N, Stebbins, Glenn T, Hagerman, Randi J, Fahn, Stanley, Berry-Kravis, Elizabeth, Leehey, Maureen A

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Coronavirus Disease 2019: Associated Multiple Organ Damage de réir Collange, Olivier, Tacquard, Charles, Delabranche, Xavier, Leonard-Lorant, Ian, Ohana, Mickaël, Onea, Mihaela, Anheim, Mathieu, Solis, Morgane, Sauer, Arnaud, Baloglu, Seyyid, Pessaux, Patrick, Ohlmann, Patrick, Kaeuffer, Charlotte, Oulehri, Walid, Kremer, Stephane, Mertes, Paul Michel

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Spastic paraplegia due to recessive or dominant mutations in ERLIN2 can convert to ALS de réir Amador, Maria-Del-Mar, Muratet, François, Teyssou, Elisa, Banneau, Guillaume, Danel-Brunaud, Véronique, Allart, Etienne, Antoine, Jean-Christophe, Camdessanché, Jean-Philippe, Anheim, Mathieu, Rudolf, Gabrielle, Tranchant, Christine, Fleury, Marie-Céline, Bernard, Emilien, Stevanin, Giovanni, Millecamps, Stéphanie

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Delirium and encephalopathy in severe COVID-19: a cohort analysis of ICU patients de réir Helms, Julie, Kremer, Stéphane, Merdji, Hamid, Schenck, Malika, Severac, François, Clere-Jehl, Raphaël, Studer, Antoine, Radosavljevic, Mirjana, Kummerlen, Christine, Monnier, Alexandra, Boulay, Clotilde, Fafi-Kremer, Samira, Castelain, Vincent, Ohana, Mickaël, Anheim, Mathieu, Schneider, Francis, Meziani, Ferhat

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

The GRIA3 c.2477G > A Variant Causes an Exaggerated Startle Reflex, Chorea, and Multifocal Myoclonus de réir Piard, Juliette, Béreau, Matthieu, XiangWei, Wenshu, Wirth, Thomas, Amsallem, Daniel, Buisson, Lauren, Richard, Philippe, Liu, Nana, Xu, Yuchen, Myers, Scott J., Traynelis, Stephen F., Chelly, Jameleddine, Anheim, Mathieu, Raynaud, Martine, Van Maldergem, Lionel, Yuan, Hongjie

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease de réir Hirst, Jennifer, Edgar, James R., Esteves, Typhaine, Darios, Frédéric, Madeo, Marianna, Chang, Jaerak, Roda, Ricardo H., Dürr, Alexandra, Anheim, Mathieu, Gellera, Cinzia, Li, Jun, Züchner, Stephan, Mariotti, Caterina, Stevanin, Giovanni, Blackstone, Craig, Kruer, Michael C., Robinson, Margaret S.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease de réir Prud'hon, Sabine, Bekadar, Samir, Rastetter, Agnès, Guégan, Justine, Cormier-Dequaire, Florence, Lacomblez, Lucette, Mangone, Graziella, You, Hana, Daniau, Mailys, Marie, Yannick, Bertrand, Hélène, Lesage, Suzanne, Tezenas Du Montcel, Sophie, Anheim, Mathieu, Brice, Alexis, Danjou, Fabrice, Corvol, Jean-Christophe

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation de réir Kim, Christine Y., Wirth, Thomas, Hubsch, Cécile, Németh, Andrea H., Okur, Volkan, Anheim, Mathieu, Drouot, Nathalie, Tranchant, Christine, Rudolf, Gabrielle, Chelly, Jamel, Tatton-Brown, Katrina, Blauwendraat, Cornelis, Vonsattel, Jean Paul G., Cortes, Etty, Alcalay, Roy N., Chung, Wendy K.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update de réir Patterson, Marc C., Clayton, Peter, Gissen, Paul, Anheim, Mathieu, Bauer, Peter, Bonnot, Olivier, Dardis, Andrea, Dionisi-Vici, Carlo, Klünemann, Hans-Hermann, Latour, Philippe, Lourenço, Charles M., Ory, Daniel S., Parker, Alasdair, Pocoví, Miguel, Strupp, Michael, Vanier, Marie T., Walterfang, Mark, Marquardt, Thorsten

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán