Canlyniadau Chwilio - Lesage, Suzanne

Synaptojanin 1 Mutation in Parkinson's Disease Brings Further Insight into the Neuropathological Mechanisms gan Drouet, Valérie, Lesage, Suzanne

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Familial Parkinson's Disease/Parkinsonism gan Tomiyama, Hiroyuki, Lesage, Suzanne, Tan, Eng-King, Jeon, Beom S.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

The four diagnostic criteria for Restless Legs Syndrome are unable to exclude confounding conditions (“mimics”) gan Hening, Wayne A., Allen, Richard P., Washburn, Mystinna, Lesage, Suzanne R., Earley, Christopher J.

Cael y testun llawn Cael y testun llawn Cael y testun llawn

LRRK2 Haplotype Analyses in European and North African Families with Parkinson Disease: A Common Founder for the G2019S Mutation Dating from the 13th Century gan Lesage, Suzanne , Leutenegger, Anne-Louise , Ibanez, Pablo , Janin, Sabine , Lohmann, Ebba , Dürr, Alexandra , Brice, Alexis 

Cael y testun llawn Cael y testun llawn

The Normal Parkin Sequence gan Ren, Yong, Liu, Xiaojun, Lesage, Suzanne, Cai, Miao, Pu, Jiali, Zhang, Baorong, Brice, Alexis, Feng, Jian

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Editorial: Celebrating the Diversity of Genetic Research to Dissect the Pathogenesis of Parkinson's Disease gan Farrer, Matthew J., Bardien, Soraya, Hattori, Nobutaka, Lesage, Suzanne, Ross, Owen A., Mellick, George D., Kruger, Rejko

Cael y testun llawn Cael y testun llawn Cael y testun llawn

EIF4G1 mutations do not cause Parkinson’s disease gan Nichols, Noah, Bras, Jose M, Hernandez, Dena G, Jansen, Iris E, Lesage, Suzanne, Lubbe, Steven, Singleton, Andrew B

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Clinical Variability of SYNJ1-Associated Early-Onset Parkinsonism gan Lesage, Suzanne, Mangone, Graziella, Tesson, Christelle, Bertrand, Hélène, Benmahdjoub, Mustapha, Kesraoui, Selma, Arezki, Mohamed, Singleton, Andrew, Corvol, Jean-Christophe, Brice, Alexis

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Does the Expression and Epigenetics of Genes Involved in Monogenic Forms of Parkinson’s Disease Influence Sporadic Forms? gan Lanore, Aymeric, Lesage, Suzanne, Mariani, Louise-Laure, Menon, Poornima Jayadev, Ravassard, Philippe, Cheval, Helene, Corti, Olga, Brice, Alexis, Corvol, Jean-Christophe

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Sleep Disturbance in Heavy Marijuana Users gan Bolla, Karen I., Lesage, Suzanne R., Gamaldo, Charlene E., Neubauer, David N., Funderburk, Frank R., Cadet, Jean Lud, David, Paula M., Verdejo-Garcia, Antonio, Benbrook, Amy R.

Cael y testun llawn Cael y testun llawn

Polysomnogram Changes in Marijuana Users Reporting Sleep Disturbances during Prior Abstinence gan Bolla, Karen I., Lesage, Suzanne R., Gamaldo, Charlene E., Neubauer, David N., Wang, Nae-Yuh, Funderburk, Frank R., Allen, Richard P., David, Paula M., Cadet, Jean Lud

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel gan Bouhouche, Ahmed, Tesson, Christelle, Regragui, Wafaa, Rahmani, Mounia, Drouet, Valérie, Tibar, Houyam, Souirti, Zouhayr, Ben El Haj, Rafiqua, Bouslam, Naima, Yahyaoui, Mohamed, Brice, Alexis, Benomar, Ali, Lesage, Suzanne

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Mechanisms of Genomic Instabilities Underlying Two Common Fragile-Site-Associated Loci, PARK2 and DMD, in Germ Cell and Cancer Cell Lines gan Mitsui, Jun, Takahashi, Yuji, Goto, Jun, Tomiyama, Hiroyuki, Ishikawa, Shunpei, Yoshino, Hiroyo, Minami, Narihiro, Smith, David I., Lesage, Suzanne, Aburatani, Hiroyuki, Nishino, Ichizo, Brice, Alexis, Hattori, Nobutaka, Tsuji, Shoji

Cael y testun llawn Cael y testun llawn Cael y testun llawn

A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism gan Edvardson, Simon, Cinnamon, Yuval, Ta-Shma, Asaf, Shaag, Avraham, Yim, Yang-In, Zenvirt, Shamir, Jalas, Chaim, Lesage, Suzanne, Brice, Alexis, Taraboulos, Albert, Kaestner, Klaus H., Greene, Lois E., Elpeleg, Orly

Cael y testun llawn Cael y testun llawn Cael y testun llawn

C9orf72 repeat expansions are a rare genetic cause of parkinsonism gan Lesage, Suzanne, Le Ber, Isabelle, Condroyer, Christel, Broussolle, Emmanuel, Gabelle, Audrey, Thobois, Stéphane, Pasquier, Florence, Mondon, Karl, Dion, Patrick A., Rochefort, Daniel, Rouleau, Guy A., Dürr, Alexandra, Brice, Alexis

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man gan Saint-Aubert, Laure, Pariente, Jérémie, Dumas, Herve, Payoux, Pierre, Brandel, Jean-Philippe, Puel, Michèle, Vital, Anne, Guedj, Eric, Lesage, Suzanne, Peoc’h, Katell, Brefel Courbon, Christine, Ory Magne, Fabienne

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Gene–environment interaction modulated by allelic heterogeneity in inflammatory diseases gan Chamaillard, Mathias, Philpott, Dana, Girardin, Stephen E., Zouali, Habib, Lesage, Suzanne, Chareyre, Fabrice, Bui, The Hung, Giovannini, Marco, Zaehringer, Ulrich, Penard-Lacronique, Virginie, Sansonetti, Philippe J., Hugot, Jean-Pierre, Thomas, Gilles

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease gan Lesage, Suzanne, Bras, Jose, Cormier-Dequaire, Florence, Condroyer, Christel, Nicolas, Aude, Darwent, Lee, Guerreiro, Rita, Majounie, Elisa, Federoff, Monica, Heutink, Peter, Wood, Nicholas W., Gasser, Thomas, Hardy, John, Tison, François, Singleton, Andrew, Brice, Alexis

Cael y testun llawn Cael y testun llawn Cael y testun llawn

Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease gan 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

Cael y testun llawn Cael y testun llawn Cael y testun llawn

CARD15/NOD2 Mutational Analysis and Genotype-Phenotype Correlation in 612 Patients with Inflammatory Bowel Disease gan Lesage, Suzanne, Zouali, Habib, Cézard, Jean-Pierre, Colombel, Jean-Frédéric, Belaiche, Jacques, Almer, Sven, Tysk, Curt, O’Morain, Colm, Gassull, Miquel, Binder, Vibeke, Finkel, Yigael, Modigliani, Robert, Gower-Rousseau, Corinne, Macry, Jeanne, Merlin, Françoise, Chamaillard, Mathias, Jannot, Anne-Sophie, Thomas, Gilles, Hugot, Jean-Pierre

Cael y testun llawn Cael y testun llawn