Progressive Ataxia and Palatal Tremor: Think about POLG Mutations

Por Mongin, Marie, Delorme, Cécile, Lenglet, Timothée, Jardel, Claude, Vignal, Catherine, Roze, Emmanuel
Publicado no Tremor Other Hyperkinet Mov (N Y) (2016)

Tremor Associated with Chronic Inflammatory Demyelinating Polyneuropathy and Anti‐Neurofascin‐155 Antibodies

Por Bailly, Laurent, Mongin, Marie, Delorme, Cecile, Apartis, Emmanuelle, Saheb, Samir, Viala, Karine, Roze, Emmanuel
Publicado no Tremor Other Hyperkinet Mov (N Y) (2018)

Motor Timing in Tourette Syndrome: The Effect of Movement Lateralization and Bimanual Coordination

Por Martino, Davide, Hartmann, Andreas, Pelosin, Elisa, Lagravinese, Giovanna, Delorme, Cecile, Worbe, Yulia, Avanzino, Laura
Publicado no Front Neurol (2019)

Explicit Agency in Patients with Cervical Dystonia: Altered Recognition of Temporal Discrepancies between Motor Actions and Their Feedback

Por Delorme, Cécile, Roze, Emmanuel, Grabli, David, Mayer, Jean-Michel, Degos, Bertrand, Vidailhet, Marie, Worbe, Yulia
Publicado no PLoS One (2016)

Glycosphingolipid Binding Specificities of Rotavirus: Identification of a Sialic Acid-Binding Epitope

Por Delorme, Cécile, Brüssow, Harald, Sidoti, Josette, Roche, Niamh, Karlsson, Karl-Anders, Neeser, Jean-Richard, Teneberg, Susann
Publicado em 2001

Specific effect of a dopamine partial agonist on counterfactual learning: evidence from Gilles de la Tourette syndrome

Por Salvador, Alexandre, Worbe, Yulia, Delorme, Cécile, Coricelli, Giorgio, Gaillard, Raphaël, Robbins, Trevor W., Hartmann, Andreas, Palminteri, Stefano
Publicado no Sci Rep (2017)

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions

Por Rouzier, Cécile, Moore, David, Delorme, Cécile, Lacas-Gervais, Sandra, Ait-El-Mkadem, Samira, Fragaki, Konstantina, Burté, Florence, Serre, Valérie, Bannwarth, Sylvie, Chaussenot, Annabelle, Catala, Martin, Yu-Wai-Man, Patrick, Paquis-Flucklinger, Véronique
Publicado no Hum Mol Genet (2017)

A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca(2+) homeostasis and ER-mitochondria interactions

Por Rouzier, Cécile, Moore, David, Delorme, Cécile, Lacas-Gervais, Sandra, Ait-El-Mkadem, Samira, Fragaki, Konstantina, Burté, Florence, Serre, Valérie, Bannwarth, Sylvie, Chaussenot, Annabelle, Catala, Martin, Yu-Wai-Man, Patrick, Paquis-Flucklinger, Véronique
Publicado no Hum Mol Genet (2017)

Cryptic amyloidogenic elements in mutant NEFH causing Charcot-Marie-Tooth 2 trigger aggresome formation and neuronal death

Por Jacquier, Arnaud, Delorme, Cécile, Belotti, Edwige, Juntas-Morales, Raoul, Solé, Guilhem, Dubourg, Odile, Giroux, Marianne, Maurage, Claude-Alain, Castellani, Valérie, Rebelo, Adriana, Abrams, Alexander, Züchner, Stephan, Stojkovic, Tanya, Schaeffer, Laurent, Latour, Philippe
Publicado no Acta Neuropathol Commun (2017)