Segregation of ATP10B variants in families with autosomal recessive parkinsonism von Tesson, Christelle, Lohmann, Ebba, Devos, David, Bertrand, Hélène, Lesage, Suzanne, Brice, Alexis

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study von Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Romdhan, Sawssan Ben, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Toullec, Benjamin Le, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohamed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Tazir, Meriem, Djebara, Mouna Ben, Gouider, Riadh, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean‐Christophe, Brice, Alexis, Lesage, Suzanne, Lunati, Ariane, Houot, Marion, Ben Romdhan, Sawssan, Clot, Fabienne, Tesson, Christelle, Mangone, Graziella, Le Toullec, Benjamin, Courtin, Thomas, Larcher, Kathy, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouhouche, Ahmed, Anheim, Mathieu, Roze, Emmanuel, Viallet, François, Tison, François, Broussolle, Emmanuel, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Ben Djebara, Mouna, Gouider, Riadh, Tazir, Meriem, Tranchant, Christine, Vidailhet, Marie, Le Guern, Eric, Corti, Olga, Mhiri, Chokri, Lohmann, Ebba, Singleton, Andy, Corvol, Jean‐Christophe, Brice, Alexis

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Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families von Courtin, Thomas, Tesson, Christelle, Corvol, Jean-Christophe, Lesage, Suzanne, Brice, Alexis

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Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease von Smaili, Imane, Tesson, Christelle, Regragui, Wafa, Bertrand, Hélène, Rahmani, Mounia, Bouslam, Naima, Benomar, Ali, Brice, Alexis, Lesage, Suzanne, Bouhouche, Ahmed

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Mutations in KCND3 cause spinocerebellar ataxia type 22 von Lee, Yi-Chung, Durr, Alexandra, Majczenko, Karen, Huang, Yen-Hua, Liu, Yu-Chao, Lien, Cheng-Chang, Tsai, Pei-Chien, Ichikawa, Yaeko, Goto, Jun, Monin, Marie-Lorraine, Li, Jun Z., Chung, Ming-Yi, Mundwiller, Emeline, Shakkottai, Vikram, Liu, Tze-Tze, Tesson, Christelle, Lu, Yi-Chun, Brice, Alexis, Tsuji, Shoji, Burmeister, Margit, Stevanin, Giovanni, Soong, Bing-Wen

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

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PLA2G6‐associated late‐onset parkinsonism in a Sudanese family von Bakhit, Yousuf, Tesson, Christelle, Ibrahim, Mohamed O., Eltom, Khalid, Eltazi, Isra, Elsayed, Liena E.O., Lesage, Suzanne, Seidi, Osheik, Corvol, Jean‐Christophe, Wüllner, Ullrich

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Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort von Lesage, Suzanne, Houot, Marion, Mangone, Graziella, Tesson, Christelle, Bertrand, Hélène, Forlani, Sylvie, Anheim, Mathieu, Brefel-Courbon, Christine, Broussolle, Emmanuel, Thobois, Stéphane, Damier, Philippe, Durif, Franck, Roze, Emmanuel, Tison, François, Grabli, David, Ory-Magne, Fabienne, Degos, Bertrand, Viallet, François, Cormier-Dequaire, Florence, Ouvrard-Hernandez, Anne-Marie, Vidailhet, Marie, Lohmann, Ebba, Singleton, Andrew, Corvol, Jean-Christophe, Brice, Alexis

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Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice von CHORT, Alice, ALVES, Sandro, RUBERG, Merle, JANER, Alexandre, STEVANIN, Giovanni, BRICE, Alexis, SITTLER, Annie, MARINELLO, Martina, DUFRESNOIS, Béatrice, DORNBIERER, Jean-Gabriel, TESSON, Christelle, LATOUCHE, Morwena, BAKER, Darren P, BARKATS, Martine, EL HACHIMI, Khalid H

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SUMOylation by SUMO2 is implicated in the degradation of misfolded ataxin-7 via RNF4 in SCA7 models von Marinello, Martina, Werner, Andreas, Giannone, Mariagiovanna, Tahiri, Khadija, Alves, Sandro, Tesson, Christelle, den Dunnen, Wilfred, Seeler, Jacob-S, Brice, Alexis, Sittler, Annie

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Genotype–phenotype correlation in PRKN-associated Parkinson’s disease von Menon, Poornima Jayadev, Sambin, Sara, Criniere-Boizet, Baptiste, Courtin, Thomas, Tesson, Christelle, Casse, Fanny, Ferrien, Melanie, Mariani, Louise-Laure, Carvalho, Stephanie, Lejeune, Francois-Xavier, Rebbah, Sana, Martet, Gaspard, Houot, Marion, Lanore, Aymeric, Mangone, Graziella, Roze, Emmanuel, Vidailhet, Marie, Aasly, Jan, Gan Or, Ziv, Yu, Eric, Dauvilliers, Yves, Zimprich, Alexander, Tomantschger, Volker, Pirker, Walter, Álvarez, Ignacio, Pastor, Pau, Di Fonzo, Alessio, Bhatia, Kailash P., Magrinelli, Francesca, Houlden, Henry, Real, Raquel, Quattrone, Andrea, Limousin, Patricia, Korlipara, Prasad, Foltynie, Thomas, Grosset, Donald, Williams, Nigel, Narendra, Derek, Lin, Hsin-Pin, Jovanovic, Carna, Svetel, Marina, Lynch, Timothy, Gallagher, Amy, Vandenberghe, Wim, Gasser, Thomas, Brockmann, Kathrin, Morris, Huw R., Borsche, Max, Klein, Christine, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Corvol, Jean Christophe

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Proxy-analysis of the genetics of cognitive decline in Parkinson’s disease through polygenic scores von Faouzi, Johann, Tan, Manuela, Casse, Fanny, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Mangone, Graziella, Mariani, Louise-Laure, Iwaki, Hirotaka, Colliot, Olivier, Pihlstrøm, Lasse, Corvol, Jean-Christophe

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Lack of Evidence for a Role of Genetic Variation in TMEM230 in the Risk for Parkinson’s disease in the Caucasian Population von Giri, Anamika, MS, Mok, Kin Y., FRCP, Jansen, Iris, MS, Sharma, Manu, PhD, Tesson, Christelle, PhD, Mangone, Graziella, MD, PhD, Lesage, Suzanne, PhD, Bras, José M., PhD, Shulman, Josua, PhD, Sheerin, Una-Marie, MRCP, Díez-Fairen, Mónica, MS, Pastor, Pau, MD, PhD, Tolosa, Eduardo, MD, PhD, Ferreira, Joaquim, MD, PhD, Amin, Najaf, PhD, van Duijn, Cornelia M., PhD, van Rooij, Jeroen, BSc, Uitterlinden, André G., PhD, Kraaij, Robert, PhD, Nalls, Michael, PhD, Simón-Sánchez, Javier, PhD

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Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology von Tesson, Christelle, Koht, Jeanette, Stevanin, Giovanni

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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel von 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

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LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease von Bonello, Fiona, Hassoun, Sidi-Mohamed, Mouton-Liger, François, Shin, Yea Seul, Muscat, Adeline, Tesson, Christelle, Lesage, Suzanne, Beart, Philip M, Brice, Alexis, Krupp, Johannes, Corvol, Jean-Christophe, Corti, Olga

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Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease von Tesson, Christelle, Bouchetara, Mohamed Sofiane, Ferrien, Mélanie, Lesage, Suzanne, Brice, Alexis

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Confirmation of RAB32 Ser71Arg Involvement in Parkinson's Disease von Cogan, Guillaume, Tesson, Christelle, Brefel-Courbon, Christine, Lanore, Aymeric, Kodjovi, Gatepe Cedoine, Welment, Lisa, Clot, Fabienne, Lesage, Suzanne, Brice, Alexis

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A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies von Coutelier, Marie, Coarelli, Giulia, Monin, Marie-Lorraine, Konop, Juliette, Davoine, Claire-Sophie, Tesson, Christelle, Valter, Rémi, Anheim, Mathieu, Behin, Anthony, Castelnovo, Giovanni, Charles, Perrine, David, Albert, Ewenczyk, Claire, Fradin, Mélanie, Goizet, Cyril, Hannequin, Didier, Labauge, Pierre, Riant, Florence, Sarda, Pierre, Sznajer, Yves, Tison, François, Ullmann, Urielle, Van Maldergem, Lionel, Mochel, Fanny, Brice, Alexis, Stevanin, Giovanni, Durr, Alexandra

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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses von Gustavsson, Emil K, Follett, Jordan, Trinh, Joanne, Barodia, Sandeep K, Real, Raquel, Liu, Zhiyong, Grant-Peters, Melissa, Fox, Jesse D, Appel-Cresswell, Silke, Stoessl, A Jon, Rajput, Alex, Rajput, Ali H, Auer, Roland, Tilney, Russel, Sturm, Marc, Haack, Tobias B, Lesage, Suzanne, Tesson, Christelle, Brice, Alexis, Vilariño-Güell, Carles, Ryten, Mina, Goldberg, Matthew S, West, Andrew B, Hu, Michele T, Morris, Huw R, Sharma, Manu, Gan-Or, Ziv, Samanci, Bedia, Lis, Pawel, Periñan, Maria Teresa, Amouri, Rim, Ben Sassi, Samia, Hentati, Faycel, Tonelli, Francesca, Alessi, Dario R, Farrer, Matthew J

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