Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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  • Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4
    Kessler, Christoph; Serna-Higuita, Lina Maria; Wilke, Carlo; Rattay, Tim W.; Hengel, Holger; Reichbauer, Jennifer; Stransky, Elke; Leyva-Gutierrez, Alejandra; Mengel, David; Synofzik, Matthis; Schoels, Ludger; Martus, Peter; Schuele, Rebecca (2022)
  • Characterizing POLG Ataxia: Clinics, Electrophysiology and Imaging
    Synofzik, Matthis; Srulijes, Karin; Godau, Jana; Berg, Daniela; Schoels, Ludger (2012)
  • Characterizing the Clinical Features and Atrophy Patterns of MAPT-Related Frontotemporal Dementia With Disease Progression Modeling
    Young, Alexandra L.; Bocchetta, Martina; Russell, Lucy L.; Convery, Rhian S.; Peakman, Georgia; Todd, Emily; Cash, David M.; Greaves, Caroline V.; van Swieten, John; Jiskoot, Lize; Seelaar, Harro; Moreno, Fermin; Sanchez-Valle, Raquel; Borroni, Barbara; Laforce, Robert, Jr.; Masellis, Mario; Tartaglia, Maria Carmela; Graff, Caroline; Galimberti, Daniela; Rowe, James B.; Finger, Elizabeth; Synofzik, Matthis; Vandenberghe, Rik; de Mendonca, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Chris; Gerhard, Alex; Levin, Johannes; Danek, Adrian; Otto, Markus; Sorbi, Sandro; Williams, Steven C. R.; Alexander, Daniel C.; Rohrer, Jonathan D. (2021)
  • Clinical and genetic characteristics of sporadic adult-onset degenerative ataxia
    Giordano, Ilaria; Harmuth, Florian; Jacobi, Heike; Paap, Brigitte; Vielhaber, Stefan; Machts, Judith; Schoels, Ludger; Synofzik, Matthis; Sturm, Marc; Tallaksen, Chantal; Wedding, Iselin M.; Boesch, Sylvia; Eigentler, Andreas; van de Warrenburg, Bart; van Gaalen, Judith; Kamm, Christoph; Dudesek, Ales; Kang, Jun-Suk; Timmann, Dagmar; Silvestri, Gabriella; Masciullo, Marcella; Klopstock, Thomas; Neuhofer, Christiane; Ganos, Christos; Filla, Alessandro; Bauer, Peter; du Montcel, Sophie Tezenas; Klockgether, Thomas (2017)
  • 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)
  • 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)
  • 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)
  • 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)
  • 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)
  • Decreased retinal sensitivity and loss of retinal nerve fibers in multiple system atrophy
    Fischer, M. Dominik; Synofzik, Matthis; Kernstock, Christoph; Dietzsch, Janko; Heidlauf, Robert; Schicks, Julia; Srulijes, Karin; Wiethoff, Sarah; Menn, Oliver; Berg, Daniela; Schoels, Ludger; Schiefer, Ulrich (2013)
  • Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
    Pellerin, D.; Danzi, M. C.; Wilke, C.; Renaud, M.; Fazal, S.; Dicaire, M. -J; Scriba, C. K.; Ashton, C.; Yanick, C.; Beijer, D.; Rebelo, A.; Rocca, C.; Jaunmuktane, Z.; Sonnen, J. A.; Lariviere, R.; Genis, D.; Porcel, L. Molina; Choquet, K.; Sakalla, R.; Provost, S.; Robertson, R.; Allard-Chamard, X.; Tetreault, M.; Reiling, S. J.; Nagy, S.; Nishadham, V; Purushottam, M.; Vengalil, S.; Bardhan, M.; Nalini, A.; Chen, Z.; Mathieu, J.; Massie, R.; Chalk, C. H.; Lafontaine, A. -L; Evoy, F.; Rioux, M. -F; Ragoussis, J.; Boycott, K. M.; Dube, M. -P; Duquette, A.; Houlden, H.; Ravenscroft, G.; Laing, N. G.; Lamont, P. J.; Saporta, M. A.; Schuele, R.; Schoels, L.; La Piana, R.; Synofzik, M.; Zuchner, S.; Brais, B. (2023)
  • Diagnostic accuracy of research criteria for prodromal frontotemporal dementia
    Benussi, Alberto; Premi, Enrico; Grassi, Mario; Alberici, Antonella; Cantoni, Valentina; Gazzina, Stefano; Archetti, Silvana; Gasparotti, Roberto; Fumagalli, Giorgio G.; Bouzigues, Arabella; Russell, Lucy L.; Samra, Kiran; Cash, David M.; Bocchetta, Martina; Todd, Emily G.; Convery, Rhian S.; Swift, Imogen; Sogorb-Esteve, Aitana; Heller, Carolin; van Swieten, John C.; Jiskoot, Lize C.; Seelaar, Harro; Sanchez-Valle, Raquel; Moreno, Fermin; Laforce, Jr Robert; Graff, Caroline; Synofzik, Matthis; Galimberti, Daniela; Rowe, James B.; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; Mendonca, Alexandre; Tiraboschi, Pietro; Butler, Chris R.; Santana, Isabel; Gerhard, Alexander; Le Ber, Isabelle; Pasquier, Florence; Ducharme, Simon; Levin, Johannes; Sorbi, Sandro; Otto, Markus; Padovani, Alessandro; Rohrer, Jonathan D.; Borroni, Barbara (2024)
  • Differential early subcortical involvement in genetic FTD within the GENFI cohort
    Bocchetta, Martina; Todd, Emily G.; Peakman, Georgia; Cash, David M.; Convery, Rhian S.; Russell, Lucy L.; Thomas, David L.; Iglesias, Juan Eugenio; van Swieten, John C.; Jiskoot, Lize C.; Seelaar, Harro; Borroni, Barbara; Galimberti, Daniela; Sanchez-Valle, Raquel; Laforce, Robert; Moreno, Fermin; Synofzik, Matthis; Graff, Caroline; Masellis, Mario; Tartaglia, Maria Carmela; Rowe, James B.; Vandenberghe, Rik; Finger, Elizabeth; Tagliavini, Fabrizio; de Mendonca, Alexandre; Santana, Isabel; Butler, Chris R.; Ducharme, Simon; Gerhard, Alexander; Danek, Adrian; Levin, Johannes; Otto, Markus; Sorbi, Sandro; Le Ber, Isabelle; Pasquier, Florence; Rohrer, Jonathan D. (2021)
  • Digital Gait Biomarkers Allow to Capture 1-Year Longitudinal Change in Spinocerebellar Ataxia Type 3
    Ilg, Winfried; Mueller, Bjoern; Faber, Jennifer; van Gaalen, Judith; Hengel, Holger; Vogt, Ina R.; Hennes, Guido; van de Warrenburg, Bart; Klockgether, Thomas; Schoels, Ludger; Synofzik, Matthis (2022)
  • Disease-related cortical thinning in presymptomatic granulin mutation carriers
    Borrego-Ecija, Sergi; Sala-Llonch, Roser; van Swieten, John; Borroni, Barbara; Moreno, Fermin; Masellis, Mario; Tartaglia, Carmela; Graff, Caroline; Galimberti, Daniela; Laforce, Robert, Jr.; Rowe, James B.; Finger, Elizabeth; Vandenberghe, Rik; Tagliavini, Fabrizio; de Mendonca, Alexandre; Santana, Isabel; Synofzik, Matthis; Ducharme, Simon; Levin, Johannes; Danek, Adrian; Gerhard, Alex; Otto, Markus; Butler, Chris; Frisoni, Giovanni; Sorbi, Sandro; Heller, Carolin; Bocchetta, Martina; Cash, David M.; Convery, Rhian S.; Moore, Katrina M.; Rohrer, Jonathan D.; Sanchez-Valle, Raquel (2021)