Browsing Universitätsbibliographie by Author "Wilke, Carlo"

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Browsing Universitätsbibliographie by Author "Wilke, Carlo"

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  • 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 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)
  • 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)
  • Atypical parkinsonism in C9orf72 expansions: a case report and systematic review of 45 cases from the literature
    Wilke, Carlo; Pomper, Joern K.; Biskup, Saskia; Puskas, Cornelia; Berg, Daniela; Synofzik, Matthis (2016)
  • 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)
  • 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)
  • 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)
  • Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
    Pottier, Cyril; Ren, Yingxue; Perkerson, Ralph B., III; Baker, Matt; Jenkins, Gregory D.; van Blitterswijk, Marka; DeJesus-Hernandez, Mariely; van Rooij, Jeroen G. J.; Murray, Melissa E.; Christopher, Elizabeth; McDonnell, Shannon K.; Fogarty, Zachary; Batzler, Anthony; Tian, Shulan; Vicente, Cristina T.; Matchett, Billie; Karydas, Anna M.; Hsiung, Ging-Yuek Robin; Seelaar, Harro; Mol, Merel O.; Finger, Elizabeth C.; Graff, Caroline; Oijerstedt, Linn; Neumann, Manuela; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Prudlo, Johannes; Rizzu, Patrizia; Simon-Sanchez, Javier; Edbauer, Dieter; Roeber, Sigrun; Diehl-Schmid, Janine; Evers, Bret M.; King, Andrew; Mesulam, M. Marsel; Weintraub, Sandra; Geula, Changiz; Bieniek, Kevin F.; Petrucelli, Leonard; Ahern, Geoffrey L.; Reiman, Eric M.; Woodruff, Bryan K.; Caselli, Richard J.; Huey, Edward D.; Farlow, Martin R.; Grafman, Jordan; Mead, Simon; Grinberg, Lea T.; Spina, Salvatore; Grossman, Murray; Irwin, David J.; Lee, Edward B.; Suh, EunRan; Snowden, Julie; Mann, David; Ertekin-Taner, Nilufer; Uitti, Ryan J.; Wszolek, Zbigniew K.; Josephs, Keith A.; Parisi, Joseph E.; Knopman, David S.; Petersen, Ronald C.; Hodges, John R.; Piguet, Olivier; Geier, Ethan G.; Yokoyama, Jennifer S.; Rissman, Robert A.; Rogaeva, Ekaterina; Keith, Julia; Zinman, Lorne; Tartaglia, Maria Carmela; Cairns, Nigel J.; Cruchaga, Carlos; Ghetti, Bernardino; Kofler, Julia; Lopez, Oscar L.; Beach, Thomas G.; Arzberger, Thomas; Herms, Jochen; Honig, Lawrence S.; Vonsattel, Jean Paul; Halliday, Glenda M.; Kwok, John B.; White, Charles L., III; Gearing, Marla; Glass, Jonathan; Rollinson, Sara; Pickering-Brown, Stuart; Rohrer, Jonathan D.; Trojanowski, John Q.; Van Deerlin, Vivianna; Bigio, Eileen H.; Troakes, Claire; Al-Sarraj, Safa; Asmann, Yan; Miller, Bruce L.; Graff-Radford, Neill R.; Boeve, Bradley F.; Seeley, William W.; Mackenzie, Ian R. A. (2019)
  • Induced pluripotent stem cells (iPSCs) derived from cerebrotendinous xanthomatosis (CTX) patient's fibroblasts carrying a R395S mutation
    Hoeflinger, Philip; Hauser, Stefan; Theurer, Yvonne; Weissenberger, Stefanie; Wilke, Carlo; Schoels, Ludger (2016)
  • Intraindividual Neurofilament Dynamics in Serum Mark the Conversion to Sporadic Parkinson's Disease
    Wilke, Carlo; Teixeira dos Santos, Marcia Cristina; Schulte, Claudia; Deuschle, Christian; Scheller, Dieter; Verbelen, Moira; Brockmann, Kathrin; von Thaler, Anna-Katharina; Suenkel, Ulrike; Roeben, Benjamin; Bujac, Sarah; Metzger, Florian G.; Maetzler, Walter; Costa, Andre Nogueira; Synofzik, Matthis; Berg, Daniela (2020)
  • Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type
    Wilke, Carlo; Mengel, David; Schols, Ludger; Hengel, Holger; Rakowicz, Maria; Klockgether, Thomas; Durr, Alexandra; Filla, Alessandro; Melegh, Bela; Schule, Rebecca; Reetz, Kathrin; Jacobi, Heike; Synofzik, Matthis (2022)
  • Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia
    Kessler, Christoph; Serna-Higuita, Lina M.; Rattay, Tim W.; Maetzler, Walter; Wurster, Isabel; Hayer, Stefanie; Wilke, Carlo; Hengel, Holger; Reichbauer, Jennifer; Armbruster, Marcel; Schoels, Ludger; Martus, Peter; Schuele, Rebecca (2021)
  • 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)
  • Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice
    Wilke, Carlo; Haas, Eva; Reetz, Kathrin; Faber, Jennifer; Garcia-Moreno, Hector; Santana, Magda M.; van de Warrenburg, Bart; Hengel, Holger; Lima, Manuela; Filla, Alessandro; Durr, Alexandra; Melegh, Bela; Masciullo, Marcella; Infante, Jon; Giunti, Paola; Neumann, Manuela; de Vries, Jeroen; de Almeida, Luis Pereira; Rakowicz, Maria; Jacobi, Heike; Schule, Rebecca; Kaeser, Stephan A.; Kuhle, Jens; Klockgether, Thomas; Schoels, Ludger; Barro, Christian; Huebener-Schmid, Jeannette; Synofzik, Matthis (2020)
  • NfL and pNfH are increased in Friedreich's ataxia
    Hayer, Stefanie Nicole; Liepelt, Inga; Barro, Christian; Wilke, Carlo; Kuhle, Jens; Martus, Peter; Schoels, Ludger; Schulz, Joerg Bernhard; Reetz, Kathrin; Fedosov, Kathrin; Didszun, Claire; Klockgether, Thomas; Giordano, Ilaria; Pandolfo, Massimo; Depondt, Chantal; Rai, Myriam; Boesch, Sylvia; Nachbauer, Wolfgang; Eigentler, Andreas; Indelicato, Elisabetta; Giunti, Paola; Parkinson, Michael; Manso, Katarina; Thomas-Black, Gilbert; Garcia-Moreno, Hector; Solanky, Nita; Abeti, Rosella; Polke, James; Labrum, Robin; Garrido, Rodriguez de Rivera Francisco Javier; Mascias, Javier; Velasco, Sanchez Sara; Garcia, Secades Sergio; Mariotti, Caterina; Nanetti, Lorenzo; Castaldo, Anna; Mongelli, Alessia; Fichera, Mario; Klopstock, Thomas; Karin, Ivan; Stendel, Claudia; Radelfahr, Florentine; Durr, Alexandra; Biet, Marie; Charles, Perrine; Ewenczyk, Claire; Just, Jennifer; Koutsis, Georgios; Walsh, Richard; Bertini, Enrico (2020)
  • 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)