Axonal transport deficits and neurodegenerative diseases von Millecamps, Stéphanie, Julien, Jean-Pierre

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Modifying macrophages at the periphery has the capacity to change microglial reactivity and to extend ALS survival von Chiot, Aude, Zaïdi, Sakina, Iltis, Charlène, Ribon, Matthieu, Berriat, Félix, Schiaffino, Lorenzo, Jolly, Ariane, de la Grange, Pierre, Mallat, Michel, Bohl, Delphine, Millecamps, Stéphanie, Seilhean, Danielle, Lobsiger, Christian S., Boillée, Séverine

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Oxidation of SQSTM1/p62 mediates the link between redox state and protein homeostasis von Carroll, Bernadette, Otten, Elsje G., Manni, Diego, Stefanatos, Rhoda, Menzies, Fiona M., Smith, Graham R., Jurk, Diana, Kenneth, Niall, Wilkinson, Simon, Passos, Joao F., Attems, Johannes, Veal, Elizabeth A., Teyssou, Elisa, Seilhean, Danielle, Millecamps, Stéphanie, Eskelinen, Eeva-Liisa, Bronowska, Agnieszka K., Rubinsztein, David C., Sanz, Alberto, Korolchuk, Viktor I.

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Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology von Teyssou, Elisa, Takeda, Takahiro, Lebon, Vincent, Boillée, Séverine, Doukouré, Brahima, Bataillon, Guillaume, Sazdovitch, Véronique, Cazeneuve, Cécile, Meininger, Vincent, LeGuern, Eric, Salachas, François, Seilhean, Danielle, Millecamps, Stéphanie

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ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS von Sproviero, William, Shatunov, Aleksey, Stahl, Daniel, Shoai, Maryam, van Rheenen, Wouter, Jones, Ashley R, Al-Sarraj, Safa, Andersen, Peter M, Bonini, Nancy M, Conforti, Francesca L, Van Damme, Philip, Daoud, Hussein, Del Mar Amador, Maria, Fogh, Isabella, Forzan, Monica, Gaastra, Ben, Gellera, Cinzia, Gitler, Aaron D, Hardy, John, Fratta, Pietro, La Bella, Vincenzo, Le Ber, Isabelle, Van Langenhove, Tim, Lattante, Serena, Lee, Yi-Chung, Malaspina, Andrea, Meininger, Vincent, Millecamps, Stèphanie, Orrell, Richard, Rademakers, Rosa, Robberecht, Wim, Rouleau, Guy, Ross, Owen A, Salachas, Francois, Sidle, Katie, Smith, Bradley N, Soong, Bing-Wen, Sorarù, Gianni, Stevanin, Giovanni, Kabashi, Edor, Troakes, Claire, van Broeckhoven, Christine, Veldink, Jan H, van den Berg, Leonard H, Shaw, Christopher E, Powell, John F, Al-Chalabi, Ammar

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Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia von Freischmidt, Axel, Wieland, Thomas, Richter, Benjamin, Ruf, Wolfgang, Schaeffer, Veronique, Müller, Kathrin, Marroquin, Nicolai, Nordin, Frida, Hübers, Annemarie, Weydt, Patrick, Pinto, Susana, Press, Rayomond, Millecamps, Stéphanie, Molko, Nicolas, Bernard, Emilien, Desnuelle, Claude, Soriani, Marie-Hélène, Dorst, Johannes, Graf, Elisabeth, Nordström, Ulrika, Feiler, Marisa S., Putz, Stefan, Boeckers, Tobias M., Meyer, Thomas, Winkler, Andrea S., Winkelman, Juliane, de Carvalho, Mamede, Thal, Dietmar R., Otto, Markus, Brännström, Thomas, Volk, Alexander E, Kursula, Petri, Danzer, Karin M., Lichtner, Peter, Dikic, Ivan, Meitinger, Thomas, Ludolph, Albert C., Strom, Tim M., Andersen, Peter M., Weishaupt, Jochen H.

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Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis von Teyssou, Elisa, Muratet, François, Amador, Maria-Del-Mar, Ferrien, Mélanie, Lautrette, Géraldine, Machat, Selma, Boillée, Séverine, Larmonier, Thierry, Saker, Safaa, Leguern, Eric, Cazeneuve, Cécile, Marie, Yannick, Guegan, Justine, Gyorgy, Beata, Cintas, Pascal, Meininger, Vincent, Le Forestier, Nadine, Salachas, François, Couratier, Philippe, Camu, William, Seilhean, Danielle, Millecamps, Stéphanie

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SQSTM1 Mutations in French Patients With Frontotemporal Dementia or Frontotemporal Dementia With Amyotrophic Lateral Sclerosis von Le Ber, Isabelle, Camuzat, Agnès, Guerreiro, Rita, Bouya-Ahmed, Kawtar, Bras, Jose, Nicolas, Gael, Gabelle, Audrey, Didic, Mira, De Septenville, Anne, Millecamps, Stéphanie, Lenglet, Timothée, Latouche, Morwena, Kabashi, Edor, Campion, Dominique, Hannequin, Didier, Hardy, John, Brice, Alexis

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Transactive response DNA-binding protein 43 is enriched at the centrosome in human cells von Bodin, Alexia, Greibill, Logan, Gouju, Julien, Letournel, Franck, Pozzi, Silvia, Julien, Jean-Pierre, Renaud, Laurence, Bohl, Delphine, Millecamps, Stéphanie, Verny, Christophe, Cassereau, Julien, Lenaers, Guy, Chevrollier, Arnaud, Tassin, Anne-Marie, Codron, Philippe

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Novel UBQLN2 mutations linked to amyotrophic lateral sclerosis and atypical hereditary spastic paraplegia phenotype through defective HSP70-mediated proteolysis von Teyssou, Elisa, Chartier, Laura, Amador, Maria-Del-Mar, Lam, Roselina, Lautrette, Géraldine, Nicol, Marie, Machat, Selma, Da Barroca, Sandra, Moigneu, Carine, Mairey, Mathilde, Larmonier, Thierry, Saker, Safaa, Dussert, Christelle, Forlani, Sylvie, Fontaine, Bertrand, Seilhean, Danielle, Bohl, Delphine, Boillée, Séverine, Meininger, Vincent, Couratier, Philippe, Salachas, François, Stevanin, Giovanni, Millecamps, Stéphanie

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Neurofilament accumulations in amyotrophic lateral sclerosis patients’ motor neurons impair axonal initial segment integrity von Lefebvre-Omar, Cynthia, Liu, Elise, Dalle, Carine, d’Incamps, Boris Lamotte, Bigou, Stéphanie, Daube, Clément, Karpf, Léa, Davenne, Marc, Robil, Noémie, Jost Mousseau, Coline, Blanchard, Stéphane, Tournaire, Guillaume, Nicaise, Charles, Salachas, François, Lacomblez, Lucette, Seilhean, Danielle, Lobsiger, Christian S., Millecamps, Stéphanie, Boillée, Séverine, Bohl, Delphine

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Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes von Millecamps, Stéphanie, Boillée, Séverine, Le Ber, Isabelle, Seilhean, Danielle, Teyssou, Elisa, Giraudeau, Marine, Moigneu, Carine, Vandenberghe, Nadia, Danel-Brunaud, Véronique, Corcia, Philippe, Pradat, Pierre-François, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaelle, Camu, William, Brice, Alexis, Cazeneuve, Cécile, LeGuern, Eric, Meininger, Vincent, Salachas, François

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TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts von Le Ber, Isabelle, De Septenville, Anne, Millecamps, Stéphanie, Camuzat, Agnès, Caroppo, Paola, Couratier, Philippe, Blanc, Frédéric, Lacomblez, Lucette, Sellal, François, Fleury, Marie-Céline, Meininger, Vincent, Cazeneuve, Cécile, Clot, Fabienne, Flabeau, Olivier, LeGuern, Eric, Brice, Alexis

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Adolescence/adult onset MTHFR deficiency may manifest as isolated and treatable distinct neuro-psychiatric syndromes von Gales, Ana, Masingue, Marion, Millecamps, Stephanie, Giraudier, Stephane, Grosliere, Laure, Adam, Claude, Salim, Claudio, Navarro, Vincent, Nadjar, Yann

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Integrative genetic analysis illuminates ALS heritability and identifies risk genes von Megat, Salim, Mora, Natalia, Sanogo, Jason, Roman, Olga, Catanese, Alberto, Alami, Najwa Ouali, Freischmidt, Axel, Mingaj, Xhuljana, De Calbiac, Hortense, Muratet, François, Dirrig-Grosch, Sylvie, Dieterle, Stéphane, Van Bakel, Nick, Müller, Kathrin, Sieverding, Kirsten, Weishaupt, Jochen, Andersen, Peter Munch, Weber, Markus, Neuwirth, Christoph, Margelisch, Markus, Sommacal, Andreas, Van Eijk, Kristel R., Veldink, Jan H., Lautrette, Géraldine, Couratier, Philippe, Camuzat, Agnès, Le Ber, Isabelle, Grassano, Maurizio, Chio, Adriano, Boeckers, Tobias, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Millecamps, Stéphanie, Kabashi, Edor, Storkebaum, Erik, Sellier, Chantal, Dupuis, Luc

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Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disorders von Lattante, Serena, Millecamps, Stéphanie, Stevanin, Giovanni, Rivaud-Péchoux, Sophie, Moigneu, Carine, Camuzat, Agnès, Da Barroca, Sandra, Mundwiller, Emeline, Couarch, Philippe, Salachas, François, Hannequin, Didier, Meininger, Vincent, Pasquier, Florence, Seilhean, Danielle, Couratier, Philippe, Danel-Brunaud, Véronique, Bonnet, Anne-Marie, Tranchant, Christine, LeGuern, Eric, Brice, Alexis, Le Ber, Isabelle, Kabashi, Edor

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Electrophysiological Characterization of C9ORF72-Associated Amyotrophic Lateral Sclerosis: A Retrospective Study von Pegat, Antoine, Bouhour, Françoise, Mouzat, Kevin, Vial, Christophe, Pegat, Benoit, Leblanc, Pascal, Broussolle, Emmanuel, Millecamps, Stéphanie, Lumbroso, Serge, Bernard, Emilien

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Increased prevalence of granulovacuolar degeneration in C9orf72 mutation von Riku, Yuichi, Duyckaerts, Charles, Boluda, Susana, Plu, Isabelle, Le Ber, Isabelle, Millecamps, Stéphanie, Salachas, François, Yoshida, Mari, Ando, Takashi, Katsuno, Masahisa, Sobue, Gen, Seilhean, Danielle

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Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations von Theuriet, Julian, Pegat, Antoine, Leblanc, Pascal, Vukusic, Sandra, Cazeneuve, Cecile, Millecamps, Stephanie, Banneau, Guillaume, Guillaud-Bataille, Marine, Bernard, Emilien

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Screening of OPTN in French familial amyotrophic lateral sclerosis von Millecamps, Stéphanie, Boillée, Séverine, Chabrol, Elodie, Camu, William, Cazeneuve, Cécile, Salachas, François, Pradat, Pierre-François, Danel-Brunaud, Véronique, Vandenberghe, Nadia, Corcia, Philippe, Le Forestier, Nadine, Lacomblez, Lucette, Bruneteau, Gaëlle, Seilhean, Danielle, Brice, Alexis, Feingold, Josué, Meininger, Vincent, LeGuern, Eric

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