A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia von Coutelier, Marie, Blesneac, Iulia, Monteil, Arnaud, Monin, Marie-Lorraine, Ando, Kunie, Mundwiller, Emeline, Brusco, Alfredo, Le Ber, Isabelle, Anheim, Mathieu, Castrioto, Anna, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Lory, Philippe, Stevanin, Giovanni

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Homozygous GRN mutations: new phenotypes and new insights into pathological and molecular mechanisms von Huin, Vincent, Barbier, Mathieu, Bottani, Armand, Lobrinus, Johannes Alexander, Clot, Fabienne, Lamari, Foudil, Chat, Laureen, Rucheton, Benoît, Fluchère, Frédérique, Auvin, Stéphane, Myers, Peter, Gelot, Antoinette, Camuzat, Agnès, Caillaud, Catherine, Jornéa, Ludmila, Forlani, Sylvie, Saracino, Dario, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Le Ber, Isabelle

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Homozygous TREM2 mutation in a family with atypical frontotemporal dementia von Le Ber, Isabelle, De Septenville, Anne, Guerreiro, Rita, Bras, José, Camuzat, Agnès, Caroppo, Paola, Lattante, Serena, Couarch, Philippe, Kabashi, Edor, Bouya-Ahmed, Kawtar, Dubois, Bruno, Brice, Alexis

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Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification von NICOLAS, Gaël, POTTIER, Cyril, MARTINAUD, Olivier, DEFEBVRE, Luc, KRYSTKOWIAK, Pierre, PARIENTE, Jérémie, CLANET, Michel, LABAUGE, Pierre, AYRIGNAC, Xavier, LEFAUCHEUR, Romain, LE BER, Isabelle, FREBOURG, Thierry, MALTETE, David, HANNEQUIN, Didier, CAMPION, Dominique, COUTANT, Sophie, ROVELET-LECRUX, Anne, LEGALLIC, Solenn, ROUSSEAU, Stéphane, VASCHALDE, Yvan, GUYANT-MARECHAL, Lucie, AUGUSTIN, Jérôme

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Neurofilament light chain: a biomarker for genetic frontotemporal dementia von Meeter, Lieke H., Dopper, Elise G., Jiskoot, Lize C., Sanchez‐Valle, Raquel, Graff, Caroline, Benussi, Luisa, Ghidoni, Roberta, Pijnenburg, Yolande A., Borroni, Barbara, Galimberti, Daniela, Laforce, Robert Jr, Masellis, Mario, Vandenberghe, Rik, Ber, Isabelle Le, Otto, Markus, Minkelen, Rick, Papma, Janne M., Rombouts, Serge A., Balasa, Mircea, Öijerstedt, Linn, Jelic, Vesna, Dick, Katrina M., Cash, David M., Harding, Sophie R., Jorge Cardoso, M., Ourselin, Sebastien, Rossor, Martin N., Padovani, Alessandro, Scarpini, Elio, Fenoglio, Chiara, Tartaglia, Maria C., Lamari, Foudil, Barro, Christian, Kuhle, Jens, Rohrer, Jonathan D., Teunissen, Charlotte E., Swieten, John C.

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Loss of function of C9orf72 causes motor deficits in a zebrafish model of amyotrophic lateral sclerosis von Ciura, Sorana, Lattante, Serena, Le Ber, Isabelle, Latouche, Morwena, Tostivint, Hervé, Brice, Alexis, Kabashi, Edor

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Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients von Chaussenot, Annabelle, Le Ber, Isabelle, Ait-El-Mkadem, Samira, Camuzat, Agnès, de Septenville, Anne, Bannwarth, Sylvie, Genin, Emmanuelle C, Serre, Valérie, Augé, Gaëlle, Brice, Alexis, Pouget, Jean, Paquis-Flucklinger, Véronique

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TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration von Benajiba, Lina, Le Ber, Isabelle, Camuzat, Agnès, Lacoste, Mathieu, Thomas-Anterion, Catherine, Couratier, Philippe, Legallic, Solenn, Salachas, François, Hannequin, Didier, Decousus, Marielle, Lacomblez, Lucette, Guedj, Eric, Golfier, Véronique, Camu, William, Dubois, Bruno, Campion, Dominique, Meininger, Vincent, Brice, Alexis

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CSF sTREM2 is elevated in a subset in GRN-related frontotemporal dementia von van der Ende, Emma L., Morenas-Rodriguez, Estrella, McMillan, Corey, Grossman, Murray, Irwin, David, Sanchez-Valle, Raquel, Graff, Caroline, Vandenberghe, Rik, Pijnenburg, Yolande A.L., Laforce, Robert, Ber, Isabelle Le, Lleo, Alberto, Haass, Christian, Suarez-Calvet, Marc, van Swieten, John C., Seelaar, Harro

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SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease von Nicolas, G, Charbonnier, C, Wallon, D, Quenez, O, Bellenguez, C, Grenier-Boley, B, Rousseau, S, Richard, A-C, Rovelet-Lecrux, A, Le Guennec, K, Bacq, D, Garnier, J-G, Olaso, R, Boland, A, Meyer, V, Deleuze, J-F, Amouyel, P, Munter, H M, Bourque, G, Lathrop, M, Frebourg, T, Redon, R, Letenneur, L, Dartigues, J-F, Génin, E, Lambert, J-C, Hannequin, D, Campion, D

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Inflammatory plasma profile in genetic symptomatic and presymptomatic Frontotemporal Dementia − A GENFI study von Fenoglio, Chiara, Serpente, Maria, Arcaro, Marina, Carandini, Tiziana, Sacchi, Luca, Pintus, Manuela, Rotondo, Emanuela, Borracci, Vittoria, Ghezzi, Laura, Bouzigues, Arabella, Russell, Lucy L., Foster, Phoebe H., Ferry-Bolder, Eve, van Swieten, John C., Jiskoot, Lize C., Seelaar, Harro, Sánchez Valle, Raquel, Laforce, Robert, Graff, Caroline, Vandenberghe, Rik, de Mendonça, Alexandre, Tiraboschi, Pietro, Santana, Isabel, Gerhard, Alexander, Levin, Johannes, Sorbi, Sandro, Otto, Markus, Pasquier, Florence, Ducharme, Simon, Butler, Chris R., Ber, Isabelle Le, Finger, Elizabeth, Carmela Tartaglia, Maria, Masellis, Mario, Rowe, James B., Synofzik, Matthis, Moreno, Fermin, Borroni, Barbara, Rohrer, Jonathan D., Arighi, Andrea, Galimberti, Daniela

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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement von BANNWARTH, Sylvie, AIT-EL-MKADEM, Samira, VERSCHUEREN, Annie, ROUZIER, Cecile, LE BER, Isabelle, AUGE, Gaëlle, COCHAUD, Charlotte, LESPINASSE, Françoise, N'GUYEN, Karine, DE SEPTENVILLE, Anne, BRICE, Alexis, YU-WAI-MAN, Patrick, CHAUSSENOT, Annabelle, SESAKI, Hiromi, POUGET, Jean, PAQUIS-FLUCKLINGER, Véronique, GENIN, Emmanuelle C, LACAS-GERVAIS, Sandra, FRAGAKI, Konstantina, BERG-ALONSO, Laetitia, KAGEYAMA, Yusuke, SERRE, Valérie, MOORE, David G

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Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers von Wallon, David, Boluda, Susana, Rovelet-Lecrux, Anne, Thierry, Manon, Lagarde, Julien, Miguel, Laetitia, Lecourtois, Magalie, Bonnevalle, Antoine, Sarazin, Marie, Bottlaender, Michel, Mula, Mathieu, Marty, Serge, Nakamura, Natsuko, Schramm, Catherine, Sellal, François, Jonveaux, Thérèse, Heitz, Camille, Le Ber, Isabelle, Epelbaum, Stéphane, Magnin, Eloi, Zarea, Aline, Rousseau, Stéphane, Quenez, Olivier, Hannequin, Didier, Clavaguera, Florence, Campion, Dominique, Duyckaerts, Charles, Nicolas, Gaël

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Questioning the causality of HTT CAG-repeat expansions in FTD/ALS von Thomas, Quentin, Coarelli, Giulia, Heinzmann, Anna, Le Ber, Isabelle, Amador, Maria del Mar, Durr, Alexandra

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Presymptomatic spinal cord pathology in c9orf72 mutation carriers: A longitudinal neuroimaging study von Querin, Giorgia, Bede, Peter, El Mendili, Mohamed Mounir, Li, Menghan, Pélégrini‐Issac, Mélanie, Rinaldi, Daisy, Catala, Martin, Saracino, Dario, Salachas, François, Camuzat, Agnes, Marchand‐Pauvert, Véronique, Cohen‐Adad, Julien, Colliot, Olivier, Le Ber, Isabelle, Pradat, Pierre‐François

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Structural brain splitting is a hallmark of Granulin-related frontotemporal dementia von Gazzina, Stefano, Grassi, Mario, Premi, Enrico, Alberici, Antonella, Benussi, Alberto, Cash, David M., Todd, Emily G., Peakman, Georgia, Convery, Rhian S., van Swieten, John C., Jiskoot, Lize C., Seelaar, Harro, Sanchez-Valle, Raquel, Moreno, Fermin, Laforce, Robert, Graff, Caroline, Synofzik, Matthis, Rowe, James B., Tartaglia, Maria Carmela, Finger, Elizabeth, de Mendonça, Alexandre, Butler, Chris R., Gerhard, Alexander, Ber, Isabelle Le, Pasquier, Florence, Ducharme, Simon, Levin, Johannes, Danek, Adrian, Sorbi, Sandro, Otto, Markus, Borroni, Barbara, Almeida, Maria Rosario, Andersson, Christin, Balasa, Mircea, Barandiaran, Myriam, Bargalló, Nuria, Bartha, Robart, Bender, Benjamin, Bertrand, Anne, Bessi, Valentina, Borrego-Ecija, Sergi, Bras, Jose, Brice, Alexis, Bruffaerts, Rose, Camuzat, Agnès, Cantoni, Valentina, Caroppo, Paola, Castelo-Branco, Miguel, Colliot, Olivier, Cope, Thomas, Deramecourt, Vincent, Fede, Giuseppe Di, Díez, Alina, Duro, Diana, Fenoglio, Chiara, Ferrari, Camilla, Ferreira, Catarina B., Fox, Nick, Freedman, Morris, Funkiewiez, Aurélie, Gabilondo, Alazne, Gauthier, Serge, Gorostidi, Ana, Guerreiro, Rita, Heller, Carolin, Hoegen, Tobias, Jelic, Vesna, Keren, Ron, Langheinrich, Tobias, Lebouvier, Thibaud, Leitão, Maria João, Lladó, Albert, Lombardi, Gemma, Maruta, Carolina, Mitchell, Sara, Nacmias, Benedetta, Öijerstedt, Linn, Olives, Jaume, Panman, Jessica, Papma, Janne M., Polito, Cristina, Prioni, Sara, Prix, Catharina, Rademakers, Rosa, Redaelli, Veronica, Rogaeva, Ekaterina, Rollin, Adeline, Rossi, Giacomina, Saracino, Dario, Sayah, Sabrina, Tábuas-Pereira, Miguel, Tainta, Mikel, Tang-Wai, David, Thompson, Paul, Timberlake, Carolyn, Tiraboschi, Pietro, Veldsman, Michele, Verdelho, Ana, Warren, Jason, Wlasich, Elisabeth

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Temporal dynamics predict symptom onset and cognitive decline in familial frontotemporal dementia von Malpetti, Maura, Jones, P. Simon, Ghosh, Boyd C. P., Coyle‐Gilchrist, Ian, Seelaar, Harro, Jiskoot, Lize, Sanchez‐Valle, Raquel, Moreno, Fermin, Laforce, Robert, Graff, Caroline, Synofzik, Matthis, Galimberti, Daniela, Vandenberghe, Rik, Mendonça, Alexandre, Tagliavini, Fabrizio, Butler, Chris R., Santana, Isabel, Gerhard, Alexander, Levin, Johannes, Otto, Markus, Sorbi, Sandro, Pasquier, Florence, Bouzigues, Arabella, Russell, Lucy L., Rowe, James B., Esteve, Aitana Sogorb, Bouzigues, Arabella, Greaves, Caroline V, Cash, David, Thomas, David L, Swift, Imogen J, Nicholas, Jennifer, Russell, Lucy L, Bocchetta, Martina, Shafei, Rachelle, Convery, Rhian S, Timberlake, Carolyn, Rittman, Timothy, Benussi, Alberto, Premi, Enrico, Gazzina, Stefano, Cantoni, Valentina, Arighi, Andrea, Scarpini, Elio, Borracci, Vittoria, Di Fede, Giuseppe, Caroppo, Paola, Prioni, Sara, Redaelli, Veronica, Castelo‐Branco, Miguel, Freedman, Morris, Keren, Ron, Mitchell, Sara, Shoesmith, Christen, Bartha, Robart, Poos, Jackie, Papma, Janne M., Minkelen, Rick, Ferrari, Camilla, Bessi, Valentina, Andersson, Christin, Öijerstedt, Linn, Thompson, Paul, Lladó, Albert, Olives, Jaume, Balasa, Mircea, Maruta, Carolina, Ferreira, Catarina B., Miltenberger, Gabriel, Simões do Couto, Frederico, Gabilondo, Alazne, Gorostidi, Ana, Villanua, Jorge, Tainta, Mikel, Zulaica, Miren, Barandiaran, Myriam, Alves, Patricia, Bender, Benjamin, Graf, Lisa, Vandenbulcke, Mathieu, Van Damme, Philip, Poesen, Koen, Camuzat, Agnès, Brice, Alexis, Bertrand, Anne, Funkiewiez, Aurélie, Rinaldi, Daisy, Sayah, Sabrina, Wlasich, Elisabeth, Hoegen, Tobias, Anderl‐Straub, Sarah, Rollin, Adeline, Kuchcinski, Gregory, Bertoux, Maxime, Lebouvier, Thibaud, Deramecourt, Vincent, Santiago, Beatriz, Duro, Diana, Tábuas‐Pereira, Miguel, Polyakova, Maryna

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New Antibody-Free Mass Spectrometry-Based Quantification Reveals That C9ORF72 Long Protein Isoform Is Reduced in the Frontal Cortex of Hexanucleotide-Repeat Expansion Carriers von Viodé, Arthur, Fournier, Clémence, Camuzat, Agnès, Fenaille, François, Latouche, Morwena, Elahi, Fanny, Le Ber, Isabelle, Junot, Christophe, Lamari, Foudil, Anquetil, Vincent, Becher, François

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Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients von Millecamps, Stéphanie, De Septenville, Anne, Teyssou, Elisa, Daniau, Mailys, Camuzat, Agnès, Albert, Mélanie, LeGuern, Eric, Galimberti, Daniela, Brice, Alexis, Marie, Yannick, Le Ber, Isabelle

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Demographic, neurological and behavioural characteristics and brain perfusion SPECT in frontal variant of frontotemporal dementia von Ber, Isabelle Le, Guedj, Eric, Gabelle, Audrey, Verpillat, Patrice, Volteau, Magali, Thomas-Anterion, Catherine, Decousus, Marielle, Hannequin, Didier, Véra, Pierre, Lacomblez, Lucette, Camuzat, Agnès, Didic, Mira, Puel, Michèle, Lotterie, Jean-Albert, Golfier, Véronique, Bernard, Anne-Marie, Vercelletto, Martine, Magne, Christine, Sellal, François, Namer, Izzie, Michel, Bernard-François, Pasquier, Jacques, Salachas, François, Bochet, Jean, Brice, Alexis, Habert, Marie-Odile, Dubois, Bruno

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