Browsing Universitätsbibliographie by Author "Wilke, Carlo"

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A data-driven disease progression model of fluid biomarkers in genetic frontotemporal dementia

Wilke, Carlo; Synofzik, Matthis (2022)
A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort

Synofzik, Matthis; Karnath, Hans-Otto; Wilke, Carlo; Bender, Benjamin (2020)
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study

Synofzik, Matthis; Wilke, Carlo; Sulzer, Patricia (2020)
Atypical parkinsonism in C9orf72 expansions: a case report and systematic review of 45 cases from the literature

Wilke, Carlo; Pomper, Jörn K.; Berg, Daniela; Synofzik, Matthis (2016)
Beyond ALS and FTD : the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes

Wilke, Carlo; Hayer, Stefanie Nicole; Schüle-Freyer, Rebecca; Synofzik, Matthis (2018)
Cerebrospinal Fluid Progranulin, but Not Serum Progranulin, Is Reduced in GRN-Negative Frontotemporal Dementia

Wilke, Carlo; Deuschle, Christian; Hobert, Markus Alexander; Jansen, Iris Elisabeth; Heutink, Peter; Gasser, Thomas; Maetzler, Walter; Blauwendraat, Cornelis; Metzger, Florian G.; Synofzik, Matthis (2017)
Characteristics of serum neurofilament light chain as a biomarker in hereditary spastic paraplegia type 4

Kessler, Christoph; Serna Higuita, Lina María; Wilke, Carlo; Hengel, Holger; Reichbauer, Jennifer; Stransky, Elke; Mengel, David; Martus, Peter; Rattay, Tim Wilfried; Leyva-Gutiérrez, Alejandra; Synofzik, Matthis; Schöls, Ludger; Schüle-Freyer, Rebecca (2022)
Clinical value of cerebrospinal fluid neurofilament light chain in semantic dementia

Wilke, Carlo; Synofzik, Matthis (2019)
Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approaches

Wilke, Carlo; Stransky, Elke; Deuschle, Christian; Schüle-Freyer, Rebecca; Synofzik, Matthis (2019)
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

Neumann, Manuela Claudia; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo; Simón-Sánchez, Javier (2019)
Induced pluripotent stem cells (iPSCs) derived from cerebrotendinous xanthomatosis (CTX) patient's fibroblasts carrying a R395S mutation

Höflinger, Philip; Hauser, Stefan; Theurer, Yvonne; Weißenberger, Stefanie; Wilke, Carlo; Schöls, Ludger (2016)
Intraindividual Neurofilament Dynamics in Serum Mark the Conversion to Sporadic Parkinson's Disease

Wilke, Carlo; Schulte, Claudia; Deuschle, Christian; Brockmann, Kathrin; Metzger, Florian G.; Maetzler, Walter; Berg, Daniela; Thaler, Anna-Katharina von; Sünkel, Ulrike; Röben, Benjamin; Synofzik, Matthis (2020)
Levels of Neurofilament Light at the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type

Wilke, Carlo; Mengel, David; Schöls, Ludger; Hengel, Holger; Rakowicz, Maria; Schüle-Freyer, Rebecca; Synofzik, Matthis (2022)
Neurofilament light chain is a cerebrospinal fluid biomarker in hereditary spastic paraplegia

Wurster, Isabel; Wilke, Carlo; Hengel, Holger; Reichbauer, Jennifer; Armbruster, Marcel; Martus, Peter; Kessler, Christoph; Serna Higuita, Lina María; Rattay, Tim Wilfried; Hayer, Stefanie Nicole; Schöls, Ludger; Schüle-Freyer, Rebecca (2021)
Neurofilaments in spinocerebellar ataxia type 3: blood biomarkers at the preataxic and ataxic stage in humans and mice

Wilke, Carlo; Haas, Eva; Hengel, Holger; Neumann, Manuela Claudia; Schüle-Freyer, Rebecca; Käser, Stephan A.; Schöls, Ludger; Hübener-Schmid, Jeannette; Synofzik, Matthis (2020)
NfL and pNfH are increased in Friedreich's ataxia

Hayer, Stefanie Nicole; Liepelt, Inga; Wilke, Carlo; Martus, Peter; Just, Jennifer; Schöls, Ludger (2020)
No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients

Heutink, Peter; Wilke, Carlo; Simón-Sánchez, Javier; Synofzik, Matthis (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 Elisabeth; Schulte, Claudia; Simón-Sánchez, Javier; Bender, Benjamin; Gasser, Thomas; Maetzler, Walter; Rizzu, Patrizia; Heutink, Peter; Metzger, Florian G.; Synofzik, Matthis (2016)
Plastizität der Wahrnehmung eigener Bewegungen

Wilke, Carlo (2014)
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Neumann, Manuela Claudia; Heutink, Peter; Synofzik, Matthis; Wilke, Carlo (2018)

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