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Neuronavigated repetitive transcranial magnetic stimulation as novel mapping technique provides insights into language function in primary progressive aphasia (2022)
Müller-Sarnowski, Felix ; Sollmann, Nico ; Schröder, Axel ; Houri, Leen ; Ille, Sebastian ; Grimmer, Timo ; Krieg, Sandro M. ; Diehl-Schmid, Janine
Motor speech disorders in the nonfluent, semantic and logopenic variants of primary progressive aphasia (2021)
Staiger, Anja ; Schroeter, Matthias L. ; Ziegler, Wolfram ; Schölderle, Theresa ; Anderl-Straub, Sarah ; Danek, Adrian ; Duning, Thomas ; Fassbender, Klaus ; Fliessbach, Klaus ; Jahn, Holger ; Kasper, Elisabeth ; Kornhuber, Johannes ; Landwehrmeyer, Bernhard ; Lauer, Martin ; Lombardi, Jolina ; Ludolph, Albert ; Müller-Sarnowski, Felix ; Polyakova, Maryna ; Prix, Catharina ; Prudlo, Johannes ; Regenbrecht, Frank ; Roßmeier, Carola ; Schneider, Anja ; Wiltfang, Jens ; Otto, Markus ; Diehl-Schmid, Janine
Intrathecal antibodies against herpes simplex virus are associated with tau pathology in humans with Alzheimer’s disease: biomarkers / Novel biomarkers (2020)
Goldhardt, Oliver ; Freiberger, Robert ; Ortner, Marion ; Müller-Sarnowski, Felix ; Förstl, Hans ; Diehl‐Schmid, Janine ; Ramirez, Alfredo ; Magdolen, Viktor ; Thaler, Markus ; Grimmer, Timo
The solely A+ CSF Aβ42/40 ratio using Elecsys assays performs similar to A/T and A/N ratios in predicting amyloid PET positivity: developing topics (2020)
Grimmer, Timo ; Amft, Michaela ; Ortner, Marion ; Eichenlaub, Udo ; Goldhardt, Oliver ; Müller-Sarnowski, Felix ; Diehl‐Schmid, Janine ; Förstl, Hans ; Yakushev, Igor
Therapeutic drug monitoring of rivastigmine and donepezil under consideration of CYP2D6 genotype-dependent metabolism of donepezil (2020)
Ortner, Marion ; Stange, Marion ; Schneider, Heike ; Schröder, Charlotte ; Buerger, Katharina ; Müller, Claudia ; Müller-Sarnowski, Felix ; Diehl-Schmid, Janine ; Förstl, Hans ; Grimmer, Timo ; Steimer, Werner
Regional cerebral associations between psychometric tests and imaging biomarkers in Alzheimer’s disease (2020)
Hedderich, Dennis M. ; Drost, René ; Goldhardt, Oliver ; Ortner, Marion ; Müller-Sarnowski, Felix ; Diehl-Schmid, Janine ; Zimmer, Claus ; Förstl, Hans ; Yakushev, Igor ; Jahn, Thomas ; Grimmer, Timo
P4‐299: first proven observation of a de novo PSEN1 mutation from Germany (2014)
Müller-Sarnowski, Felix ; Meißner, Jörg ; Laub, Christoph ; Wlasich, Elisabeth ; Raiser, Theresa ; Rominger, Axel ; Biskup, Saskia ; Danek, Adrian
Interferon β-1a reduces increased interleukin-16 levels in multiple sclerosis patients (2014)
Nischwitz, S. ; Faber, H. ; Sämann, P. G. ; Domingues, H. S. ; Krishnamoorthy, G. ; Knop, M. ; Müller-Sarnowski, Felix ; Yassouridis, A. ; Weber, F.
More CLEC16A gene variants associated with multiple sclerosis (2010)
Nischwitz, S. ; Cepok, S. ; Kroner, A. ; Wolf, C. ; Knop, M. ; Müller-Sarnowski, Felix ; Pfister, H. ; Rieckmann, P. ; Hemmer, B. ; Ising, M. ; Uhr, M. ; Bettecken, T. ; Holsboer, F. ; Müller-Myhsok, B. ; Weber, F.
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis (2010)
Nischwitz, Sandra ; Cepok, Sabine ; Kroner, Antje ; Wolf, Christiane ; Knop, Matthias ; Müller-Sarnowski, Felix ; Pfister, Hildegard ; Roeske, Darina ; Rieckmann, Peter ; Hemmer, Bernhard ; Ising, Marcus ; Uhr, Manfred ; Bettecken, Thomas ; Holsboer, Florian ; Müller-Myhsok, Bertram ; Weber, Frank
A 50 kb LD block in the CLEC16A gene is highly associated with multiple sclerosis in a German population (2009)
Nischwitz, Sandra ; Cepok, S. ; Kroner, A. ; Knop, M. ; Müller-Sarnowski, Felix ; Pfister, H. ; Rieckmann, P. ; Hemmer, B. ; Ising, M. ; Uhr, M. ; Bettecken, T. ; Holsboer, F. ; Müller-Myhsok, B. ; Weber, F.
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations (2008)
Weber, F. ; Fontaine, B. ; Cournu-Rebeix, I. ; Kroner, A. ; Knop, M. ; Lutz, S. ; Müller-Sarnowski, Felix ; Uhr, M. ; Bettecken, T. ; Kohli, M. ; Ripke, S. ; Ising, M. ; Rieckmann, P. ; Brassat, D. ; Semana, G. ; Babron, M.-C. ; Mrejen, S. ; Gout, C. ; Lyon-Caen, O. ; Yaouanq, J. ; Edan, G. ; Clanet, M. ; Holsboer, F. ; Clerget-Darpoux, F. ; Müller-Myhsok, B.
Polyneuropathie durch Hyperparathyreoidismus? (2007)
Schmidt, U. ; Müller-Sarnowski, Felix ; Dzaja, A. ; Zils, E. ; Weber, F.
Ocular flutter bei HIV-assoziierter Encephalitis (2007)
Müller-Sarnowski, Felix ; Weber, F. ; Schneider, M.
Navigated repetitive Transcranial Magnetic Stimulation (nTMS) in the non fluent variant of Primary Progressive Aphasia (nfvPPA) (2020)
Müller-Sarnowski, Felix ; Houri, L. ; Sollmann, N. ; Schroeder, A. ; Krieg, S. ; Diehl-Schmid, J.
Amyloid PET, FDG-PET or MRI? - the power of different imaging biomarkers to detect progression of early Alzheimer’s disease (2019)
Ortner, Marion ; Drost, René ; Heddderich, Dennis ; Goldhardt, Oliver ; Müller-Sarnowski, Felix ; Diehl-Schmid, Janine ; Förstl, Hans ; Yakushev, Igor ; Grimmer, Timo
FV 43 repetitive navigated transcranial magnetic stimulation enables language mapping in primary progressive aphasia (2019)
Diehl-Schmid, J. ; Müller-Sarnowski, Felix ; Grimmer, T. ; Sollmann, N. ; Schröder, A. ; Negwer, C. ; Krieg, S.
Phenotypic variability in C9ORF72 mutation carriers from the german FTLD‐consortium (2016)
Diehl-Schmid, Janine ; Straub, Sarah ; Müller-Sarnowski, Felix ; Grimmer, Timo ; Otto, Markus
Three novel presenilin 1 mutations marking the wide spectrum of age at onset and clinical patterns in familial Alzheimer’s disease (2015)
Roeber, Sigrun ; Müller-Sarnowski, Felix ; Kress, Julia ; Edbauer, Dieter ; Kuhlmann, Tanja ; Tüttelmann, Frank ; Schindler, Christoph ; Winter, Pia ; Arzberger, Thomas ; Müller, Ulrich ; Danek, Adrian ; Kretzschmar, Hans A.
Alzheimer: wie man nach einer kausalen Therapie sucht (2015)
Müller-Sarnowski, Felix ; Levin, Johannes ; Danek, Adrian ; Laske, Christoph ; Preische, Oliver ; Jucker, Mathias
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