Browsing Universitätsbibliographie by Author "Wilke, Carlo"

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Browsing Universitätsbibliographie by Author "Wilke, Carlo"

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  • 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 systematic review of progranulin concentrations in biofluids in over 7,000 people-assessing the pathogenicity of GRN mutations and other influencing factors
    Swift, Imogen J.; Rademakers, Rosa; Finch, Nicole; Baker, Matt; Ghidoni, Roberta; Benussi, Luisa; Binetti, Giuliano; Rossi, Giacomina; Synofzik, Matthis; Wilke, Carlo; Mengel, David; Graff, Caroline; Takada, Leonel T.; Sanchez-Valle, Raquel; Antonell, Anna; Galimberti, Daniela; Fenoglio, Chiara; Serpente, Maria; Arcaro, Marina; Schreiber, Stefanie; Vielhaber, Stefan; Arndt, Philipp; Santana, Isabel; Almeida, Maria Rosario; Moreno, Fermin; Barandiaran, Myriam; Gabilondo, Alazne; Stubert, Johannes; Gomez-Tortosa, Estrella; Agueero, Pablo; Sainz, M. Jose; Gohda, Tomohito; Murakoshi, Maki; Kamei, Nozomu; Kittel-Schneider, Sarah; Reif, Andreas; Weigl, Johannes; Jian, Jinlong; Liu, Chuanju; Serrero, Ginette; Greither, Thomas; Theil, Gerit; Lohmann, Ebba; Gazzina, Stefano; Bagnoli, Silvia; Coppola, Giovanni; Bruni, Amalia; Quante, Mirja; Kiess, Wieland; Hiemisch, Andreas; Jurkutat, Anne; Block, Matthew S.; Carlson, Aaron M.; Brathen, Geir; Sando, Sigrid Botne; Grontvedt, Goril Rolfseng; Lauridsen, Camilla; Heslegrave, Amanda; Heller, Carolin; Abel, Emily; Gomez-Nunez, Alba; Puey, Roger; Arighi, Andrea; Rotondo, Enmanuela; Jiskoot, Lize C.; Meeter, Lieke H. H.; Duraes, Joao; Lima, Marisa; Tabuas-Pereira, Miguel; Lemos, Joao; Boeve, Bradley; Petersen, Ronald C.; Dickson, Dennis W.; Graff-Radford, Neill R.; Leber, Isabelle; Sellami, Leila; Lamari, Foudil; Clot, Fabienne; Borroni, Barbara; Cantoni, Valentina; Rivolta, Jasmine; Lleo, Alberto; Fortea, Juan; Alcolea, Daniel; Illan-Gala, Ignacio; Andres-Cerezo, Lucie; Van Damme, Philip; Clarimon, Jordi; Steinacker, Petra; Feneberg, Emily; Otto, Markus; van der Ende, Emma L.; van Swieten, John C.; Seelaar, Harro; Zetterberg, Henrik; Sogorb-Esteve, Aitana; Rohrer, Jonathan D. (2024)
  • Beyond ALS and FTD : the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
    Wilke, Carlo; Baets, Jonathan; De Bleecker, Jan L.; Deconinck, Tine; Biskup, Saskia; Hayer, Stefanie N.; Zuchner, Stephan; Schuele, Rebecca; De Jonghe, Peter; Synofzik, Matthis (2018)
  • Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia
    Wilke, Carlo; Gillardon, Frank; Deuschle, Christian; Hobert, Markus A.; Jansen, Iris E.; Metzger, Florian G.; Heutink, Peter; Gasser, Thomas; Maetzler, Walter; Blauwendraat, Cornelis; Synofzik, Matthis (2017)
  • 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)
  • 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)
  • 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)
  • Fronto-striatal alterations correlate with apathy severity in behavioral variant frontotemporal dementia
    Upadhyay, Neeraj; Spottke, Annika; Schneider, Anja; Hoffmann, Daniel C.; Frommann, Ingo; Ballarini, Tommaso; Fliessbach, Klaus; Bender, Benjamin; Heekeren, Hauke R.; Haynes, John Dylan; Ewers, Michael; Duezel, Emrah; Glanz, Wenzel; Dobisch, Laura; Buerger, Katharina; Janowitz, Daniel; Levin, Johannes; Danek, Adrian; Teipel, Stefan; Kilimann, Ingo; Synofzik, Matthis; Wilke, Carlo; Peters, Oliver; Preis, Lukas; Priller, Josef; Spruth, Eike Jakob; Jessen, Frank; Boecker, Henning (2024)
  • Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy
    Pellerin, David; Wilke, Carlo; Traschuetz, Andreas; Nagy, Sara; Curro, Riccardo; Dicaire, Marie-Josee; Garcia-Moreno, Hector; Anheim, Mathieu; Wirth, Thomas; Faber, Jennifer; Timmann, Dagmar; Depienne, Christel; Rujescu, Dan; Gazulla, Jose; Reilly, Mary M.; Giunti, Paola; Brais, Bernard; Houlden, Henry; Schoels, Ludger; Strupp, Michael; Cortese, Andrea; Synofzik, Matthis (2024)
  • Neurofilament light levels predict clinical progression and death in multiple system atrophy
    Chelban, Viorica; Nikram, Elham; Perez-Soriano, Alexandra; Wilke, Carlo; Foubert-Samier, Alexandra; Vijiaratnam, Nirosen; Guo, Tong; Jabbari, Edwin; Olufodun, Simisola; Gonzalez, Mariel; Senkevich, Konstantin; Laurens, Brice; Peran, Patrice; Rascol, Olivier; Le Traon, Anne Pavy; Todd, Emily G.; Costantini, Alyssa A.; Alikhwan, Sondos; Tariq, Ambreen; Ng, Bai Lin; Munoz, Esteban; Painous, Celia; Compta, Yaroslau; Junque, Carme; Segura, Barbara; Zhelcheska, Kristina; Wellington, Henny; Schoels, Ludger; Jaunmuktane, Zane; Kobylecki, Christopher; Church, Alistair; Hu, Michele T. M.; Rowe, James B.; Leigh, P. Nigel; Massey, Luke; Burn, David J.; Pavese, Nicola; Foltynie, Tom; Pchelina, Sofya; Wood, Nicholas; Heslegrave, Amanda J.; Zetterberg, Henrik; Bocchetta, Martina; Rohrer, Jonathan D.; Marti, Maria J.; Synofzik, Matthis; Morris, Huw R.; Meissner, Wassilios G.; Houlden, Henry (2022)
  • No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
    Baradaran-Heravi, Yalda; Dillen, Lubina; Hung Phuoc Nguyen; Van Mossevelde, Sara; Baets, Jonathan; De Jonghe, Peter; Engelborghs, Sebastiaan; De Deyn, Peter P.; Vandenbulcke, Mathieu; Vandenberghe, Rik; Van Damme, Philip; Cras, Patrick; Salmon, Eric; Synofzik, Matthis; Heutink, Peter; Wilke, Carlo; Simon-Sanchez, Javier; Rojas-Garcia, Ricard; Turon-Sans, Janina; Lleo, Alberto; Illan-Gala, Ignacio; Clarimon, Jordi; Borroni, Barbara; Padovani, Alessandro; Pastor, Pau; Diez-Fairen, Monica; Aguilar, Miquel; Gelpi, Ellen; Sanchez-Valle, Raquel; Borrego-Ecija, Sergi; Matej, Radoslav; Parobkova, Eva; Nacmias, Benedetta; Sorbi, Sandro; Bagnoli, Silvia; de Mendonca, Alexandre; Ferreira, Catarina; Fraidakis, Matthew J.; Diehl-Schmid, Janine; Alexopoulos, Panagiotis; Almeida, Maria Rosario; Santana, Isabel; Van Broeckhoven, Christine; van der Zee, Julie (2018)
  • Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants
    Blauwendraat, Cornelis; Wilke, Carlo; Jansen, Iris E.; Schulte, Claudia; Simon-Sanchez, Javier; Metzger, Florian G.; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Synofzik, Matthis (2016)
  • Sensorimotor Recalibration Depends on Attribution of Sensory Prediction Errors to Internal Causes
    Wilke, Carlo; Synofzik, Matthis; Lindner, Axel (2013)
  • Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative Disease
    Wilke, Carlo; Gillardon, Frank; Deuschle, Christian; Dubois, Evelyn; Hobert, Markus A.; vom Hagen, Jennifer Mueller; Krueger, Stefanie; Biskup, Saskia; Blauwendraat, Cornelis; Hruscha, Michael; Kaeser, Stephan A.; Heutink, Peter; Maetzler, Walter; Synofzik, Matthis (2016)
  • Serum Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Biomarkers in Primary Progressive Multiple Sclerosis and Hereditary Spastic Paraplegia Type 4
    Kessler, Christoph; Ruschil, Christoph; Abdelhak, Ahmed; Wilke, Carlo; Maleska, Aleksandra; Kuhle, Jens; Krumbholz, Markus; Kowarik, Markus C.; Schuele, Rebecca (2022)
  • Serum neurofilament light chain is increased in hereditary spastic paraplegias
    Wilke, Carlo; Rattay, Tim W.; Hengel, Holger; Zimmermann, Milan; Brockmann, Kathrin; Schoels, Ludger; Kuhle, Jens; Schuele, Rebecca; Synofzik, Matthis (2018)
  • Serum neurofilament light is increased in multiple system atrophy of cerebellar type and in repeat-expansion spinocerebellar ataxias: a pilot study
    Wilke, Carlo; Bender, Friedemann; Hayer, Stefanie N.; Brockmann, Kathrin; Schoels, Ludger; Kuhle, Jens; Synofzik, Matthis (2018)
  • Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3
    Faber, Jennifer; Berger, Moritz; Wilke, Carlo; Hubener-Schmid, Jeannette; Schaprian, Tamara; Santana, Magda M.; Grobe-Einsler, Marcus; Onder, Demet; Koyak, Berkan; Giunti, Paola; Garcia-Moreno, Hector; Gonzalez-Robles, Cristina; Lima, Manuela; Raposo, Mafalda; Melo, Ana Rosa Vieira; de Almeida, Luis Pereira; Silva, Patrick; Pinto, Maria M.; van de Warrenburg, Bart P.; van Gaalen, Judith; de Vries, Jeroen; Oz, Gulin; Joers, James M.; Synofzik, Matthis; Schols, Ludger; Riess, Olaf; Infante, Jon; Manrique, Leire; Timmann, Dagmar; Thieme, Andreas; Jacobi, Heike; Reetz, Kathrin; Dogan, Imis; Onyike, Chiadikaobi; Povazan, Michal; Schmahmann, Jeremy; Ratai, Eva-Maria; Schmid, Matthias; Klockgether, Thomas (2024)
  • Stratifying the Presymptomatic Phase of Genetic Frontotemporal Dementia by Serum NfL and pNfH: A Longitudinal Multicentre Study
    Wilke, Carlo; Reich, Selina; van Swieten, John C.; Borroni, Barbara; Sanchez-Valle, Raquel; Moreno, Fermin; Laforce, Robert; Graff, Caroline; Galimberti, Daniela; Rowe, James B.; Masellis, Mario; Tartaglia, Maria C.; Finger, Elizabeth; Vandenberghe, Rik; de Mendonca, Alexandre; Tagliavini, Fabrizio; Santana, Isabel; Ducharme, Simon; Butler, Chris R.; Gerhard, Alexander; Levin, Johannes; Danek, Adrian; Otto, Markus; Frisoni, Giovanni; Ghidoni, Roberta; Sorbi, Sandro; Bocchetta, Martina; Todd, Emily; Kuhle, Jens; Barro, Christian; Rohrer, Jonathan D.; Synofzik, Matthis (2022)
  • Total tau is increased, but phosphorylated tau not decreased, in cerebrospinal fluid in amyotrophic lateral sclerosis
    Wilke, Carlo; Deuschle, Christian; Rattay, Tim W.; Maetzler, Walter; Synofzik, Matthis (2015)