Showing 1 - 20 results of 239 for search '"Schmid, Janine"', query time: 3.42s Refine Results  

Prevalence of amyloid‐β pathology in distinct variants of primary progressive aphasia

by Bergeron, David, Gorno‐Tempini, Maria L., Rabinovici, Gil D., Santos‐Santos, Miguel A., Seeley, William, Miller, Bruce L., Pijnenburg, Yolande, Keulen, M. Antoinette, Groot, Colin, van Berckel, Bart N. M., van der Flier, Wiesje M., Scheltens, Philip, Rohrer, Jonathan D., Warren, Jason D., Schott, Jonathan M., Fox, Nick C., Sanchez‐Valle, Raquel, Grau‐Rivera, Oriol, Gelpi, Ellen, Seelaar, Harro, Papma, Janne M., van Swieten, John C., Hodges, John R., Leyton, Cristian E., Piguet, Olivier, Rogalski, Emily J., Mesulam, Marsel M., Koric, Lejla, Nora, Kristensen, Pariente, Jeéreémie, Dickerson, Bradford, Mackenzie, Ian R., Hsiung, Ging‐Yuek R., Belliard, Serge, Irwin, David J., Wolk, David A., Grossman, Murray, Jones, Matthew, Harris, Jennifer, Mann, David, Snowden, Julie S., Chrem‐Mendez, Patricio, Calandri, Ismael L., Amengual, Alejandra A., Miguet‐Alfonsi, Carole, Magnin, Eloi, Magnani, Giuseppe, Santangelo, Roberto, Deramecourt, Vincent, Pasquier, Florence, Mattsson, Niklas, Nilsson, Christer, Hansson, Oskar, Keith, Julia, Masellis, Mario, Black, Sandra E., Matías‐Guiu, Jordi A., Cabrera‐Martin, María‐Nieves, Paquet, Claire, Dumurgier, Julien, Teichmann, Marc, Sarazin, Marie, Bottlaender, Michel, Dubois, Bruno, Rowe, Christopher C., Villemagne, Victor L., Vandenberghe, Rik, Granadillo, Elias, Teng, Edmond, Mendez, Mario, Meyer, Philipp T., Frings, Lars, Lleó, Alberto, Blesa, Rafael, Fortea, Juan, Seo, Sang Won, Diehl‐Schmid, Janine, Grimmer, Timo, Frederiksen, Kristian Steen, Sánchez‐Juan, Pascual, Chételat, Gaël, Jansen, Willemijn, Bouchard, Rémi W., Laforce, Robert Jr, Visser, Pieter Jelle, Ossenkoppele, Rik
Published in Annals of neurology (01.11.2018)

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A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

by van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Engelborghs, Sebastiaan, Philtjens, Stéphanie, Vandenbulcke, Mathieu, Sleegers, Kristel, Sieben, Anne, Bäumer, Veerle, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Perneczky, Robert, Diehl-Schmid, Janine, de Mendonça, Alexandre, Miltenberger-Miltenyi, Gabriel, Pimentel, José, Graff, Caroline, Chiang, Huei-Hsin, Sanchez-Valle, Raquel, Llado, Albert, Gelpi, Ellen, Santiago, Beatriz, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, vom Hagen, Jennifer Müller, Schöls, Ludger, Heneka, Michael T., Matej, Radoslav, Parobkova, Eva, Kovacs, Gabor G., Ströbel, Thomas, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Danek, Adrian, Arzberger, Thomas, Testi, Silvia, Salmon, Eric, Santens, Patrick, Cras, Patrick, Vandenberghe, Rik, De Deyn, Peter Paul, Cruts, Marc, Van Broeckhoven, Christine, van der Zee, Julie, Dillen, Lubina, Van Langenhove, Tim, Philtjens, Stéphanie, Sleegers, Kristel, Corsmit, Ellen, Cruts, Marc, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, De Deyn, Peter P., Cras, Patrick, Vandenbulcke, Mathieu, Borroni, Barbara, Padovani, Alessandro, Archetti, Silvana, Maetzler, Walter, Heneka, Michael T., Jessen, Frank, Kurzwelly, Delia, Sachtleben, Carmen, Miltenberger-Miltenyi, Gabriel, Pereira, Sónia, Firmo, Clara, Pimentel, José, Llado, Albert, Antonell, Anna, Gelpi, Ellen, Kinhult Ståhlbom, Anne, Thonberg, Håkan, Nennesmo, Inger, Börjesson-Hanson, Anne, Bagnoli, Silvia, Sorbi, Sandro, Santiago, Beatriz, Helena Ribeiro, Maria, Garret, Carolina, Pires, Paula, Frisoni, Giovanni, Zanetti, Orazio, Bonvicini, Cristian, Sarafov, Stayko, Tournev, Ivailo, Jordanova, Albena, Ströbel, Thomas, Mairer, Wolfgang, Matej, Radoslav, Parobkova, Eva, Danel, Adrian, Arzberger, Thomas, Maria Fabrizi, Gian, Testi, Silvia, Ferrari, Sergio, Cavallaro, Tiziana, Salmon, Eric
Published in Human mutation (01.02.2013)

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TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

by der Zee, Julie, Gijselinck, Ilse, Mossevelde, Sara, Perrone, Federica, Dillen, Lubina, Heeman, Bavo, Bäumer, Veerle, Engelborghs, Sebastiaan, Bleecker, Jan, Baets, Jonathan, Gelpi, Ellen, Rojas‐García, Ricardo, Clarimón, Jordi, Lleó, Alberto, Diehl‐Schmid, Janine, Alexopoulos, Panagiotis, Perneczky, Robert, Synofzik, Matthis, Just, Jennifer, Schöls, Ludger, Graff, Caroline, Thonberg, Håkan, Borroni, Barbara, Padovani, Alessandro, Jordanova, Albena, Sarafov, Stayko, Tournev, Ivailo, Mendonça, Alexandre, Miltenberger‐Miltényi, Gabriel, Simões do Couto, Frederico, Ramirez, Alfredo, Jessen, Frank, Heneka, Michael T., Gómez‐Tortosa, Estrella, Danek, Adrian, Cras, Patrick, Vandenberghe, Rik, Jonghe, Peter, Deyn, Peter P., Sleegers, Kristel, Cruts, Marc, Broeckhoven, Christine, Goeman, Johan, Nuytten, Dirk, Smets, Katrien, Robberecht, Wim, Damme, Philip Van, Bleecker, Jan De, Santens, Patrick, Dermaut, Bart, Versijpt, Jan, Michotte, Alex, Ivanoiu, Adrian, Deryck, Olivier, Bergmans, Bruno, Delbeck, Jean, Bruyland, Marc, Willems, Christiana, Salmon, Eric, Pastor, Pau, Ortega‐Cubero, Sara, Benussi, Luisa, Ghidoni, Roberta, Binetti, Giuliano, Hernández, Isabel, Boada, Mercè, Ruiz, Agustín, Sorbi, Sandro, Nacmias, Benedetta, Bagnoli, Silvia, Sorbi, Sandro, Sanchez‐Valle, Raquel, Llado, Albert, Santana, Isabel, Rosário Almeida, Maria, Frisoni, Giovanni B, Maetzler, Walter, Matej, Radoslav, Fraidakis, Matthew J., Kovacs, Gabor G., Fabrizi, Gian Maria, Testi, Silvia
Published in Human mutation (01.03.2017)

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