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Müller-Sarnowski, Felix
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Diehl-Schmid, Janine
(7)
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(6)
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(6)
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(6)
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Title
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Author
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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