Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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  • Clinical assessment of dysphagia in neurodegeneration (CADN): development, validity and reliability of a bedside tool for dysphagia assessment
    Vogel, Adam P.; Rommel, Natalie; Sauer, Carina; Horger, Marius; Krumm, Patrick; Himmelbach, Marc; Synofzik, Matthis (2017)
  • Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies
    Masnada, Silvia; Hedrich, Ulrike B. S.; Gardella, Elena; Schubert, Julian; Kaiwar, Charu; Klee, Eric W.; Lanpher, Brendan C.; Gavrilova, Ralitza H.; Synofzik, Matthis; Bast, Thomas; Gorman, Kathleen; King, Mary D.; Allen, Nicholas M.; Conroy, Judith; Ben Zeev, Bruria; Tzadok, Michal; Korff, Christian; Dubois, Fanny; Ramsey, Keri; Narayanan, Vinodh; Serratosa, Jose M.; Giraldez, Beatriz G.; Helbig, Ingo; Marsh, Eric; O'Brien, Margaret; Bergqvist, Christina A.; Binelli, Adrian; Porter, Brenda; Zaeyen, Eduardo; Horovitz, Dafne D.; Wolff, Markus; Marjanovic, Dragan; Caglayan, Hande S.; Arslan, Mutluay; Pena, Sergio D. J.; Sisodiya, Sanjay M.; Balestrini, Simona; Syrbe, Steffen; Veggiotti, Pierangelo; Lemke, Johannes R.; Moller, Rikke S.; Lerche, Holger; Rubboli, Guido (2017)
  • Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia
    Meeter, Lieke H. H.; Steketee, Rebecca M. E.; Salkovic, Dina; Vos, Maartje E.; Grossman, Murray; McMillan, Corey T.; Irwin, David J.; Boxer, Adam L.; Rojas, Julio C.; Olney, Nicholas T.; Karydas, Anna; Miller, Bruce L.; Pijnenburg, Yolande A. L.; Barkhof, Frederik; Sanchez-Valle, Raquel; Llado, Albert; Borrego-Ecija, Sergi; Diehl-Schmid, Janine; Grimmer, Timo; Goldhardt, Oliver; Santillo, Alexander F.; Hansson, Oskar; Vestberg, Susanne; Borroni, Barbara; Padovani, Alessandro; Galimberti, Daniela; Scarpini, Elio; Rohrer, Jonathan D.; Woollacott, Ione O. C.; Synofzik, Matthis; Wilke, Carlo; de Mendonca, Alexandre; Vandenberghe, Rik; Benussi, Luisa; Ghidoni, Roberta; Binetti, Giuliano; Niessen, Wiro J.; Papma, Janne M.; Seelaar, Harro; Jiskoot, Lize C.; de Jong, Frank Jan; Kaat, Laura Donker; Del Campo, Marta; Teunissen, Charlotte E.; Bron, Esther E.; Van den Berg, Esther; Van Swieten, John C. (2019)
  • Clinico-Genetic, Imaging and Molecular Delineation of COQ8A-Ataxia: A Multicenter Study of 59 Patients
    Traschuetz, Andreas; Schirinzi, Tommaso; Laugwitz, Lucia; Murray, Nathan H.; Bingman, Craig A.; Reich, Selina; Kern, Jan; Heinzmann, Anna; Vasco, Gessica; Bertini, Enrico; Zanni, Ginevra; Durr, Alexandra; Magri, Stefania; Taroni, Franco; Malandrini, Alessandro; Baets, Jonathan; de Jonghe, Peter; de Ridder, Willem; Bereau, Matthieu; Demuth, Stephanie; Ganos, Christos; Basak, A. Nazli; Hanagasi, Hasmet; Kurul, Semra Hiz; Bender, Benjamin; Schoels, Ludger; Grasshoff, Ute; Klopstock, Thomas; Horvath, Rita; van de Warrenburg, Bart; Burglen, Lydie; Rougeot, Christelle; Ewenczyk, Claire; Koenig, Michel; Santorelli, Filippo M.; Anheim, Mathieu; Munhoz, Renato P.; Haack, Tobias; Distelmaier, Felix; Pagliarini, David J.; Puccio, Helene; Synofzik, Matthis (2020)
  • Cognitive composites for genetic frontotemporal dementia: GENFI-Cog
    Poos, Jackie M.; Moore, Katrina M.; Nicholas, Jennifer; Russell, Lucy L.; Peakman, Georgia; Convery, Rhian S.; Jiskoot, Lize C.; van der Ende, Emma; van den Berg, Esther; Papma, Janne M.; Seelaar, Harro; Pijnenburg, Yolande A. L.; Moreno, Fermin; Sanchez-Valle, Raquel; Borroni, Barbara; Laforce, Robert; Masellis, Mario; Tartaglia, Carmela; Graff, Caroline; Galimberti, Daniela; Rowe, James B.; Finger, Elizabeth; Synofzik, Matthis; Vandenberghe, Rik; de Mendonca, Alexandre; Tiraboschi, Pietro; Santana, Isabel; Ducharme, Simon; Butler, Chris; Gerhard, Alexander; Levin, Johannes; Danek, Adrian; Otto, Markus; Le Ber, Isabel; Pasquier, Florence; van Swieten, John C.; Rohrer, Jonathan D. (2022)
  • Comparative analysis of machine learning algorithms for multi-syndrome classification of neurodegenerative syndromes
    Lampe, Leonie; Niehaus, Sebastian; Huppertz, Hans-Juergen; Merola, Alberto; Reinelt, Janis; Mueller, Karsten; Anderl-Straub, Sarah; Fassbender, Klaus; Fliessbach, Klaus; Jahn, Holger; Kornhuber, Johannes; Lauer, Martin; Prudlo, Johannes; Schneider, Anja; Synofzik, Matthis; Danek, Adrian; Diehl-Schmid, Janine; Otto, Markus; Villringer, Arno; Egger, Karl; Hattingen, Elke; Hilker-Roggendorf, Rudiger; Schnitzler, Alfons; Sudmeyer, Martin; Oertel, Wolfgang; Kassubek, Jan; Hoeglinger, Gunter; Schroeter, Matthias L. (2022)
  • Comparing speech characteristics in spinocerebellar ataxias type 3 and type 6 with Friedreich ataxia
    Brendel, Bettina; Synofzik, Matthis; Ackermann, Hermann; Lindig, Tobias; Schoelderle, Theresa; Schoels, Ludger; Ziegler, Wolfram (2015)
  • Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohort
    Peakman, Georgia; Russell, Lucy L.; Convery, Rhian S.; Nicholas, Jennifer M.; Van Swieten, John C.; Jiskoot, Lize C.; Moreno, Fermin; Sanchez-Valle, Raquel; Laforce, Robert; Graff, Caroline; Masellis, Mario; Tartaglia, Maria Carmela; Rowe, James B.; Borroni, Barbara; Finger, Elizabeth; Synofzik, Matthis; Galimberti, Daniela; Vandenberghe, Rik; de Mendonca, Alexandre; Butler, Chris R.; Gerhard, Alex; Ducharme, Simon; Le Ber, Isabelle; Tagliavini, Fabrizio; Santana, Isabel; Pasquier, Florence; Levin, Johannes; Danek, Adrian; Otto, Markus; Sorbi, Sandro; Rohrer, Jonathan D. (2022)
  • Conceptual framework for the definition of preclinical and prodromal frontotemporal dementia
    Benussi, Alberto; Alberici, Antonella; Samra, Kiran; Russell, Lucy L.; Greaves, Caroline, V; Bocchetta, Martina; Ducharme, Simon; Finger, Elizabeth; Fumagalli, Giorgio; Galimberti, Daniela; Jiskoot, Lize C.; Le Ber, Isabelle; Masellis, Mario; Nacmias, Benedetta; Rowe, James B.; Sanchez-Valle, Raquel; Seelaar, Harro; Synofzik, Matthis; Rohrer, Jonathan D.; Borroni, Barbara (2022)
  • Consensus Paper: Ataxic Gait
    Cabaraux, Pierre; Agrawal, Sunil K.; Cai, Huaying; Calabro, Rocco Salvatore; Carlo, Casali; Loic, Damm; Sarah, Doss; Habas, Christophe; Horn, Anja K. E.; Ilg, Winfried; Louis, Elan D.; Mitoma, Hiroshi; Monaco, Vito; Petracca, Maria; Ranavolo, Alberto; Rao, Ashwini K.; Ruggieri, Serena; Schirinzi, Tommaso; Serrao, Mariano; Summa, Susanna; Strupp, Michael; Surgent, Olivia; Synofzik, Matthis; Tao, Shuai; Terasi, Hiroo; Torres-Russotto, Diego; Travers, Brittany; Roper, Jaimie A.; Manto, Mario (2023)
  • Consensus Paper: Management of Degenerative Cerebellar Disorders
    Ilg, W.; Bastian, A. J.; Boesch, S.; Burciu, R. G.; Celnik, P.; Claassen, J.; Feil, K.; Kalla, R.; Miyai, I.; Nachbauer, W.; Schoels, L.; Strupp, M.; Synofzik, M.; Teufel, J.; Timmann, D. (2014)
  • Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)
    Vogel, Adam P.; Rommel, Natalie; Oettinger, Andreas; Stoll, Lisa H.; Kraus, Eva-Maria; Gagnon, Cynthia; Horger, Marius; Krumm, Patrick; Timmann, Dagmar; Storey, Elsdon; Schoels, Ludger; Synofzik, Matthis (2018)
  • Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approaches
    Wilke, Carlo; Pujol-Calderon, Fani; Barro, Christian; Stransky, Elke; Blennow, Kaj; Michalak, Zuzanna; Deuschle, Christian; Jeromin, Andreas; Zetterberg, Henrik; Schuele, Rebecca; Hoglund, Kina; Kuhle, Jens; Synofzik, Matthis (2019)
  • Counterregulation of cAMP-directed kinase activities controls ciliogenesis
    Porpora, Monia; Sauchella, Simona; Rinaldi, Laura; Delle Donne, Rossella; Sepe, Maria; Torres-Quesada, Omar; Intartaglia, Daniela; Garbi, Corrado; Insabato, Luigi; Santoriello, Margherita; Bachmann, Verena A.; Synofzik, Matthis; Lindner, Herbert H.; Conte, Ivan; Stefan, Eduard; Feliciello, Antonio (2018)
  • CSF glial markers are elevated in a subset of patients with genetic frontotemporal dementia
    Woollacott, Ione O. C.; Swift, Imogen J.; Sogorb-Esteve, Aitana; Heller, Carolin; Knowles, Kathryn; Bouzigues, Arabella; Russell, Lucy L.; Peakman, Georgia; Greaves, Caroline, V; Convery, Rhian; Heslegrave, Amanda; Rowe, James B.; Borroni, Barbara; Galimberti, Daniela; Tiraboschi, Pietro; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; van Swieten, John C.; Seelaar, Harro; Jiskoot, Lize; Sorbi, Sandro; Butler, Chris R.; Graff, Caroline; Gerhard, Alexander; Laforce, Robert; Sanchez-Valle, Raquel; de Mendonca, Alexandre; Moreno, Fermin; Synofzik, Matthis; Vandenberghe, Rik; Ducharme, Simon; Le Ber, Isabelle; Levin, Johannes; Otto, Markus; Pasquier, Florence; Santana, Isabel; Zetterberg, Henrik; Rohrer, Jonathan D. (2022)
  • D90A-SOD1 ALS mimicking monoclonal gammopathy-associated ALS
    Synofzik, Matthis; Hagen, Jennifer Mueller Vom; Biskup, Saskia; Schoels, Ludger (2012)
  • Data-driven staging of genetic frontotemporal dementia using multi-modal MRI
    McCarthy, Jillian; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Laforce, Robert, Jr.; Graff, Caroline; Synofzik, Matthis; Galimberti, Daniela; Rowe, James B.; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; de Mendonca, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Butler, Chris; Gerhard, Alex; Danek, Adrian; Levin, Johannes; Otto, Markus; Frisoni, Giovanni; Ghidoni, Roberta; Sorbi, Sandro; Jiskoot, Lize C.; Seelaar, Harro; van Swieten, John C.; Rohrer, Jonathan D.; Iturria-Medina, Yasser; Ducharme, Simon (2022)
  • De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia
    Van de Vondel, Liedewei; De Winter, Jonathan; Beijer, Danique; Coarelli, Giulia; Wayand, Melanie; Palvadeau, Robin; Pauly, Martje G.; Klein, Katrin; Rautenberg, Maren; Guillot-Noel, Lena; Deconinck, Tine; Vural, Atay; Ertan, Sibel; Dogu, Okan; Uysal, Hilmi; Brankovic, Vesna; Herzog, Rebecca; Brice, Alexis; Durr, Alexandra; Klebe, Stephan; Stock, Friedrich; Bischoff, Almut Turid; Rattay, Tim W.; Sobrido, Maria-Jesus; De Michele, Giovanna; De Jonghe, Peter; Klopstock, Thomas; Lohmann, Katja; Zanni, Ginevra; Santorelli, Filippo M.; Timmerman, Vincent; Haack, Tobias B.; Zuchner, Stephan; Schuele, Rebecca; Stevanin, Giovanni; Synofzik, Matthis; Basak, A. Nazli; Baets, Jonathan (2022)
  • De novo ITPR1 variants are a recurrent cause of early-onset ataxia, acting via loss of channel function
    Synofzik, Matthis; Helbig, Katherine L.; Harmuth, Florian; Deconinck, Tine; Tanpaiboon, Pranoot; Sun, Bo; Guo, Wenting; Wang, Ruiwu; Palmaer, Erika; Tang, Sha; Schaefer, G. Bradley; Gburek-Augustat, Janina; Zuchner, Stephan; Kraegeloh-Mann, Ingeborg; Baets, Jonathan; de Jonghe, Peter; Bauer, Peter; Chen, S. R. Wayne; Schoels, Ludger; Schuele, Rebecca (2018)
  • De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
    Syrbe, Steffen; Hedrich, Ulrike B. S.; Riesch, Erik; Djemie, Tania; Mueller, Stephan; Moller, Rikke S.; Maher, Bridget; Hernandez-Hernandez, Laura; Synofzik, Matthis; Caglayan, Hande S.; Arslan, Mutluay; Serratosa, Jose M.; Nothnagel, Michael; May, Patrick; Krause, Roland; Loeffler, Heidrun; Detert, Katja; Dorn, Thomas; Vogt, Heinrich; Kraemer, Guenter; Schoels, Ludger; Mullis, Primus E.; Linnankivi, Tarja; Lehesjoki, Anna-Elina; Sterbova, Katalin; Craiu, Dana C.; Hoffman-Zacharska, Dorota; Korff, Christian M.; Weber, Yvonne G.; Steinlin, Maja; Gallati, Sabina; Bertsche, Astrid; Bernhard, Matthias K.; Merkenschlager, Andreas; Kiess, Wieland; Gonzalez, Michael; Zuechner, Stephan; Palotie, Aarno; Suls, Arvid; De Jonghe, Peter; Helbig, Ingo; Biskup, Saskia; Wolff, Markus; Maljevic, Snezana; Schule, Rebecca; Sisodiya, Sanjay M.; Weckhuysen, Sarah; Lerche, Holger; Lemke, Johannes R. (2015)