Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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Auflistung Universitätsbibliographie nach Autor "Synofzik, Matthis"

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  • 4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2-encephalopathy
    Hedrich, Ulrike B. S.; Lauxmann, Stephan; Wolff, Markus; Synofzik, Matthis; Bast, Thomas; Binelli, Adrian; Serratosa, Jose M.; Martinez-Ulloa, Pedro; Allen, Nicholas M.; King, Mary D.; Gorman, Kathleen M.; Ben Zeev, Bruria; Tzadok, Michal; Wong-Kisiel, Lily; Marjanovic, Dragan; Rubboli, Guido; Sisodiya, Sanjay M.; Lutz, Florian; Ashraf, Harshad Pannikkaveettil; Torge, Kirsten; Yan, Pu; Bosselmann, Christian; Schwarz, Niklas; Fudali, Monika; Lerche, Holger (2021)
  • A case of late-onset, thymoma-associated myasthenia gravis with ryanodine receptor and titin antibodies and concomitant granulomatous myositis
    Stefanou, M. I.; Komorowski, L.; Kade, S.; Bornemann, A.; Ziemann, U.; Synofzik, M. (2016)
  • A clinical diagnostic algorithm for early onset cerebellar ataxia
    Brandsma, R.; Verschuuren-Bemelmans, C. C.; Amrom, D.; Barisic, N.; Baxter, P.; Bertini, E.; Blumkin, L.; Brankovic-Sreckovic, V; Brouwer, O. F.; Buerk, K.; Catsman-Berrevoets, C. E.; Craiu, D.; de Coo, I. F. M.; Gburek, J.; Kennedy, C.; de Koning, T. J.; Kremer, H. P. H.; Kumar, R.; Macaya, A.; Micalizzi, A.; Mirabelli-Badenier, M.; Nemeth, A.; Nuovo, S.; Poll-The, B.; Lerman-Sagie, T.; Steinlin, M.; Synofzik, M.; Tijssen, M. A. J.; Vasco, G.; Willemsen, M. A. A. P.; Zanni, G.; Valente, E. M.; Boltshauser, E.; Sival, D. A. (2019)
  • A cognitive brain-computer interface for patients with amyotrophic lateral sclerosis
    Hohmann, M. R.; Fomina, T.; Jayaram, V.; Widmann, N.; Foerster, C.; Just, J.; Synofzik, M.; Schoelkopf, B.; Schoels, L.; Grosse-Wentrup, M. (2016)
  • A combined miRNA-piRNA signature to detect Alzheimer's disease
    Jain, Gaurav; Stuendl, Anne; Rao, Pooja; Berulava, Tea; Centeno, Tonatiuh Pena; Kaurani, Lalit; Burkhardt, Susanne; Delalle, Ivana; Kornhuber, Johannes; Huell, Michael; Maier, Wolfgang; Peters, Oliver; Esselmann, Hermann; Schulte, Claudia; Deuschle, Christian; Synofzik, Mathis; Wiltfang, Jens; Mollenhauer, Brit; Maetzler, Walter; Schneider, Anja; Fischer, Andre (2019)
  • A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia
    van der Ende, Emma L.; Bron, Esther E.; Poos, Jackie M.; Jiskoot, Lize C.; Panman, Jessica L.; Papma, Janne M.; Meeter, Lieke H.; Dopper, Elise G. P.; Wilke, Carlo; Synofzik, Matthis; Heller, Carolin; Swift, Imogen J.; Sogorb-Esteve, Aitana; Bouzigues, Arabella; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Graff, Caroline; Laforce, Robert; Galimberti, Daniela; Masellis, Mario; Tartaglia, Maria Carmela; Finger, Elizabeth; Vandenberghe, Rik; Rowe, James B.; de Mendonca, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Christopher R.; Gerhard, Alexander; Levin, Johannes; Danek, Adrian; Otto, Markus; Pijnenburg, Yolande A. L.; Sorbi, Sandro; Zetterberg, Henrik; Niessen, Wiro J.; Rohrer, Jonathan D.; Klein, Stefan; van Swieten, John C.; Venkatraghavan, Vikram; Seelaar, Harro (2022)
  • A de novo STUB1 variant associated with an early adult-onset multisystemic ataxia phenotype
    Mengel, David; Traschuetz, Andreas; Reich, Selina; Leyva-Gutierrez, Alejandra; Bender, Friedemann; Hauser, Stefan; Haack, Tobias B.; Synofzik, Matthis (2021)
  • A guide to writing systematic reviews of rare disease treatments to generate FAIR-compliant datasets: building a Treatabolome
    Atalaia, Antonio; Thompson, Rachel; Corvo, Alberto; Carmody, Leigh; Piscia, Davide; Matalonga, Leslie; Macaya, Alfons; Lochmuller, Angela; Fontaine, Bertrand; Zurek, Birte; Hernandez-Ferrer, Carles; Rheinard, Carola; Gomez-Andres, David; Desaphy, Jean-Francois; Schon, Katherine; Lohmann, Katja; Jennings, Matthew J.; Synofzik, Matthis; Riess, Olaf; Ben Yaou, Rabah; Evangelista, Teresinha; Ratnaike, Thiloka; Bros-Facer, Virginie; Gumus, Gulcin; Horvath, Rita; Chinnery, Patrick; Laurie, Steven; Graessner, Holm; Robinson, Peter; Lochmuller, Hanns; Beltran, Sergi; Bonne, Gisele (2020)
  • A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort
    Moore, Katrina; Convery, Rhian; Bocchetta, Martina; Neason, Mollie; Cash, David M.; Greaves, Caroline; Russell, Lucy L.; Clarke, Mica T. M.; Peakman, Georgia; van Swieten, John; Jiskoot, Lize; Moreno, Fermin; Barandiaran, Myriam; Sanchez-Valle, Raquel; Borroni, Barbara; Laforce, Robert, Jr.; Dore, Marie-Claire; Masellis, Mario; Tartaglia, Maria Carmela; Graff, Caroline; Galimberti, Daniela; Rowe, James B.; Finger, Elizabeth; Synofzik, Matthis; Karnath, Hans-Otto; Vandenberghe, Rik; de Mendonca, Alexandre; Maruta, Carolina; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Chris; Gerhard, Alex; Levin, Johannes; Danek, Adrian; Otto, Markus; Warren, Jason D.; Rohrer, Jonathan D.; Rossor, Martin N.; Fox, Nick C.; Woollacott, Ione O. C.; Shafei, Rachelle; Heller, Carolin; Guerreiro, Rita; Bras, Jose; Thomas, David L.; Nicholas, Jennifer; Mead, Simon; Meeter, Lieke; Panman, Jessica; Papma, Janne; van Minkelen, Rick; Pijnenburg, Yolande; Indakoetxea, Begona; Gabilondo, Alazne; Tainta, Mikel; de Arriba, Maria; Gorostidi, Ana; Zulaica, Miren; Villanua, Jorge; Diaz, Zigor; Borrego-Ecija, Sergi; Olives, Jaume; Llado, Albert; Balasa, Mircea; Antonell, Anna; Bargallo, Nuria; Premi, Enrico; Cosseddu, Maura; Gazzina, Stefano; Padovani, Alessandro; Gasparotti, Roberto; Archetti, Silvana; Black, Sandra; Mitchell, Sara; Rogaeva, Ekaterina; Freedman, Morris; Keren, Ron; Tang-Wa, David; Oijerstedt, Linn; Andersson, Christin; Jelic, Vesna; Thonberg, Hakan; Arighi, Andrea; Fenoglio, Chiara; Scarpini, Elio; Fumagalli, Giorgio; Cope, Thomas; Timberlake, Carolyn; Rittman, Timothy; Shoesmith, Christen; Bartha, Robart; Rademakers, Rosa; Wilke, Carlo; Bender, Benjamin; Bruffaerts, Rose; Van Damme, Philip; Vandenbulcke, Mathieu; Ferreira, Catarina B.; Miltenberger, Gabriel; Verdelho, Ana (2020)
  • A neuromodulation experience registry for deep brain stimulation studies inpsychiatric research: rationale and recommendations for implementation
    Fins, Joseph J.; Schlaepfer, Thomas E.; Synofzik, Matthis (2012)
  • A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
    van der Zee, Julie; Gijselinck, Ilse; Dillen, Lubina; Van Langenhove, Tim; Theuns, Jessie; Engelborghs, Sebastiaan; Philtjens, Stephanie; Vandenbulcke, Mathieu; Sleegers, Kristel; Sieben, Anne; Baumer, Veerle; Maes, Githa; Corsmit, Ellen; Borroni, Barbara; Padovani, Alessandro; Archetti, Silvana; Perneczky, Robert; Diehl-Schmid, Janine; de Mendonca, Alexandre; Miltenberger-Miltenyi, Gabriel; Pereira, Sonia; Pimentel, Jose; Nacmias, Benedetta; Bagnoli, Silvia; Sorbi, Sandro; Graff, Caroline; Chiang, Huei-Hsin; Westerlund, Marie; Sanchez-Valle, Raquel; Llado, Albert; Gelpi, Ellen; Santana, Isabel; Almeida, Maria Rosario; Santiago, Beatriz; Frisoni, Giovanni; Zanetti, Orazio; Bonvicini, Cristian; Synofzik, Matthis; Maetzler, Walter; vom Hagen, Jennifer Mueller; Schoels, Ludger; Heneka, Michael T.; Jessen, Frank; Matej, Radoslav; Parobkova, Eva; Kovacs, Gabor G.; Stroebel, Thomas; Sarafov, Stayko; Tournev, Ivailo; Jordanova, Albena; Danek, Adrian; Arzberger, Thomas; Fabrizi, Gian Maria; Testi, Silvia; Salmon, Eric; Santens, Patrick; Martin, Jean-Jacques; Cras, Patrick; Vandenberghe, Rik; De Deyn, Peter Paul; Cruts, Marc; Van Broeckhoven, Christine (2013)
  • A panel of CSF proteins separates genetic frontotemporal dementia from presymptomatic mutation carriers: a GENFI study
    Bergstrom, Sofia; Oijerstedt, Linn; Remnestal, Julia; Olofsson, Jennie; Ullgren, Abbe; Seelaar, Harro; van Swieten, John C.; Synofzik, Matthis; Sanchez-Valle, Raquel; Moreno, Fermin; Finger, Elizabeth; Masellis, Mario; Tartaglia, Carmela; Vandenberghe, Rik; Laforce, Robert; Galimberti, Daniela; Borroni, Barbara; Butler, Chris R.; Gerhard, Alexander; Ducharme, Simon; Rohrer, Jonathan D.; Manberg, Anna; Graff, Caroline; Nilsson, Peter (2021)
  • A recessive ataxia diagnosis algorithm for the next generation sequencing era
    Renaud, Mathilde; Tranchant, Christine; Torres Martin, Juan Vicente; Mochel, Fanny; Synofzik, Matthis; van de Warrenburg, Bart; Pandolfo, Massimo; Koenig, Michel; Kolb, Stefan A.; Anheim, Mathieu (2017)
  • A Recurrent Mutation in KCNA2 as a Novel Cause of Hereditary Spastic Paraplegia and Ataxia
    Helbig, Katherine L.; Hedrich, Ulrike B. S.; Shinde, Deepali N.; Krey, Ilona; Teichmann, Anne-Christin; Hentschel, Julia; Schubert, Julian; Chamberlin, Adam C.; Huether, Robert; Lu, Hsiao-Mei; Alcaraz, Wendy A.; Tang, Sha; Jungbluth, Chelsy; Dugan, Sarah L.; Vainionpaa, Leena; Karle, Kathrin N.; Synofzik, Matthis; Lehesjoki, Anna-Elina; Helbig, Ingo; Lerche, Holger; Lemke, Johannes R.; Schöls, Ludger; Schüle-Freyer, Rebecca (2016)
  • Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort
    Convery, Rhian S.; Bocchetta, Martina; Greaves, Caroline, V; Moore, Katrina M.; Cash, David M.; Van Swieten, John; 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, Christopher; Gerhard, Alex; Levin, Johannes; Danek, Adrian; Otto, Markus; Warren, Jason D.; Rohrer, Jonathan D. (2020)
  • Abnormal Paraplegin Expression in Swollen Neurites, tau- and alpha-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation
    Thal, Dietmar R.; Zuechner, Stephan; Gierer, Stephan; Schulte, Claudia; Schoels, Ludger; Schuele, Rebecca; Synofzik, Matthis (2015)
  • Absence of BiP Co-chaperone DNAJC3 Causes Diabetes Mellitus and Multisystemic Neurodegeneration
    Synofzik, Matthis; Haack, Tobias B.; Kopajtich, Robert; Gorza, Matteo; Rapaport, Doron; Greiner, Markus; Schoenfeld, Caroline; Freiberg, Clemens; Schorr, Stefan; Holl, Reinhard W.; Gonzalez, Michael A.; Fritsche, Andreas; Fallier-Becker, Petra; Zimmermann, Richard; Strom, Tim M.; Meitinger, Thomas; Zuechner, Stephan; Schuele, Rebecca; Schoels, Ludger; Prokisch, Holger (2014)
  • Absence of EEG correlates of self-referential processing depth in ALS
    Fomina, Tatiana; Weichwald, Sebastian; Synofzik, Matthis; Just, Jenifer; Schoels, Ludger; Schoelkopf, Bernhard; Grosse-Wentrup, Moritz (2017)
  • Affective coding: the emotional dimension of agency
    Gentsch, Antje; Synofzik, Matthis (2014)
  • Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
    Moore, Katrina M.; Nicholas, Jennifer; Grossman, Murray; McMillan, Corey T.; Irwin, David J.; Massimo, Lauren; Van Deerlin, Vivianna M.; Warren, Jason D.; Fox, Nick C.; Rossor, Martin N.; Mead, Simon; Bocchetta, Martina; Boeve, Bradley F.; Knopman, David S.; Graff-Radford, Neill R.; Forsberg, Leah K.; Rademakers, Rosa; Wszolek, Zbigniew K.; van Swieten, John C.; Jiskoot, Lize C.; Meeter, Lieke H.; Dopper, Elise G. P.; Papma, Janne M.; Snowden, Julie S.; Saxon, Jennifer; Jones, Matthew; Pickering-Brown, Stuart; Le Ber, Isabelle; Camuzat, Agnes; Brice, Alexis; Caroppo, Paola; Ghidoni, Roberta; Pievani, Michela; Benussi, Luisa; Binetti, Giuliano; Dickerson, Bradford C.; Lucente, Diane; Krivensky, Samantha; Graff, Caroline; Oijerstedt, Linn; Fallstrom, Marie; Thonberg, Hakan; Ghoshal, Nupur; Morris, John C.; Borroni, Barbara; Benussi, Alberto; Padovani, Alessandro; Galimberti, Daniela; Scarpini, Elio; Fumagalli, Giorgio G.; Mackenzie, Ian R.; Hsiung, Ging-Yuek R.; Sengdy, Pheth; Boxer, Adam L.; Rosen, Howie; Taylor, Joanne B.; Synofzik, Matthis; Wilke, Carlo; Sulzer, Patricia; Hodges, John R.; Halliday, Glenda; Kwok, John; Sanchez-Valle, Raquel; Llado, Albert; Borrego-Ecija, Sergi; Santana, Isabel; Almeida, Maria Rosario; Tabuas-Pereira, Miguel; Moreno, Fermin; Barandiaran, Myriam; Indakoetxea, Begona; Levin, Johannes; Danek, Adrian; Rowe, James B.; Cope, Thomas E.; Otto, Markus; Anderl-Straub, Sarah; de Mendonca, Alexandre; Maruta, Carolina; Masellis, Mario; Black, Sandra E.; Couratier, Philippe; Lautrette, Geraldine; Huey, Edward D.; Sorbi, Sandro; Nacmias, Benedetta; Laforce, Robert, Jr.; Tremblay, Marie-Pier L.; Vandenberghe, Rik; Van Damme, Philip; Rogalski, Emily J.; Weintraub, Sandra; Gerhard, Alexander; Onyike, Chiadi U.; Ducharme, Simon; Papageorgiou, Sokratis G.; Ng, Adeline Su Lyn; Brodtmann, Amy; Finger, Elizabeth; Guerreiro, Rita; Bras, Jose (2020)