Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Karin, Srulijes"'
Autor:
Minh H. Pham, Morad Elshehabi, Linda Haertner, Silvia Del Din, Karin Srulijes, Tanja Heger, Matthis Synofzik, Markus A. Hobert, Gert S. Faber, Clint Hansen, Dina Salkovic, Joaquim J. Ferreira, Daniela Berg, Álvaro Sanchez-Ferro, Jaap H. van Dieën, Clemens Becker, Lynn Rochester, Gerhard Schmidt, Walter Maetzler
Publikováno v:
Frontiers in Neurology, Vol 8 (2017)
IntroductionInertial measurement units (IMUs) positioned on various body locations allow detailed gait analysis even under unconstrained conditions. From a medical perspective, the assessment of vulnerable populations is of particular relevance, espe
Externí odkaz:
https://doaj.org/article/92754f7f1fd942348779d645b0411df8
Autor:
Karin Srulijes, Kathrin Brockmann, Senait Ogbamicael, Markus A. Hobert, Ann-Kathrin Hauser, Claudia Schulte, Jasmin Fritzen, Michael Schwenk, Thomas Gasser, Daniela Berg, Walter Maetzler
Publikováno v:
Parkinson's Disease, Vol 2017 (2017)
Introduction. Parkinson’s disease patients carrying a heterozygous mutation in the gene glucocerebrosidase (GBA-PD) show faster motor and cognitive decline than idiopathic Parkinson’s disease (iPD) patients, but the mechanisms behind this observa
Externí odkaz:
https://doaj.org/article/c6b8727626204fda83530fe4808070cd
Autor:
Karin Srulijes, Michael Schwenk, Cornelia Schatton, Lars Schwickert, Clemens Becker, Walter Maetzler, Kristin Teubner-Liepert, Srijana K C, Jochen Klenk, Miriam Meyer, Matthis Synofzik
Publikováno v:
The Cerebellum 18(3), 340-348 (2019). doi:10.1007/s12311-018-1002-x
Falls in patients with neurodegenerative diseases (NDDs) have enormous detrimental consequences. A better understanding of the interplay between physical activity (PA) and fall risk might help to reduce fall frequency. We aimed to investigate the ass
Autor:
David J. Mack, Sandra Lachenmaier, Uwe J. Ilg, Lena Stetz, Ulrike Sünkel, Andrea Pilotto, Daniela Berg, Gerhard W. Eschweiler, Karin Srulijes, Sebastian Heinzel, Leonie Gugolz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b75513fc0e0eeae57ed021a779e3dc2b
https://doi.org/10.1111/ejn.14878/v3/response1
https://doi.org/10.1111/ejn.14878/v3/response1
Autor:
Inga Liepelt-Scarfone, Susanne Gräber, Monika Fruhmann Berger, Anne Feseker, Gülsüm Baysal, Ilona Csoti, Jana Godau, Alexandra Gaenslen, Heiko Huber, Karin Srulijes, Kathrin Brockmann, Daniela Berg
Publikováno v:
International Journal of Alzheimer's Disease, Vol 2012 (2012)
Parkinson’s disease is characterized by a substantial cognitive heterogeneity, which is apparent in different profiles and levels of severity. To date, a distinct clinical profile for patients with a potential risk of developing dementia still has
Externí odkaz:
https://doaj.org/article/a31450ff06ba418f8d0d62a74f386841
Autor:
Elke Stransky, Walter Maetzler, Karin Srulijes, Ingolf Lachmann, Inga Liepelt-Scarfone, Tim W. Rattay, Claudia Schulte, Thomas Gasser, Ilona Csoti, Stefanie Lerche, Christian Deuschle, Ann-Kathrin Hauser, Kathrin Brockmann, Henrik Zetterberg, Daniela Berg, Andrea Pilotto
Publikováno v:
Movement Disorders. 32:1780-1783
Background A proportion of idiopathic Parkinson's disease patients (PDidiopathic) with dementia show altered CSF profiles of amyloid β (Aβ) and Tau. PD patients with Glucocerebrosidase (GBA) mutations (PDGBA) present with even more cognitive declin
Autor:
Claudia Schulte, Milan Zimmermann, Daniela Berg, Karin Srulijes, Ilona Csoti, Kathrin Brockmann, K. Prahl, Ann-Kathrin Hauser, Alexandra Gaenslen
Publikováno v:
European journal of neurology 26(4), 694-698 (2018). doi:10.1111/ene.13776
BACKGROUND Prevalence and time of occurrence of prodromal symptoms of Parkinson's disease (PD) in relation to the onset of classical motor manifestation varies between patients. Possible modifying factors might be different genetic architectures pred
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7605ca2c216e36c4c9e489290770bca8
Autor:
Michel Panisset, Günther Deuschl, Patrick A. Dion, Lukas Tittmann, Mark Hallett, Claudia M. Testa, Simon Girard, Zbigniew K. Wszolek, Karin Srulijes, Klaus Seppi, Susanne A. Schneider, Gregor Kuhlenbäumer, Nancy D. Merner, Juliane Winkelmann, Wolfgang Lieb, Manuela Pendziwiat, Dietrich Haubenberger, Oswaldo Lorenzo-Betancor, Franziska Hopfner, Ronald B. Postuma, Kirsten E. Zeuner, Geneviève Bernard, Sylvain Chouinard, Guy A. Rouleau, Elan D. Louis, Owen A. Ross, Eva Reischl, Thomas Arzberger, Daniela Berg, Stefanie H. Müller, Sara Ortega-Cubero, Cynthia V. Bourassa, Joshua M. Shulman, Ali H. Rajput, Alexandra I. Soto-Ortolaza, Stephan Klebe, Nicolas Dupré, Isabel Wurster, Pau Pastor, Anna Hussl, Konstantin Strauch, Karl-Heinz Ladwig, Colin A. Hodgkinson, Joseph Jankovic, Delia Lorenz, Werner Poewe, Lorraine N. Clark, Alex Rajput, Carles Vilariño-Güell
Publikováno v:
Brain 139, 3163-3169 (2016)
Brain 139(12), 3163-3169 (2016). doi:10.1093/brain/aww242
Brain 139(12), 3163-3169 (2016). doi:10.1093/brain/aww242
We conducted a genome-wide association study of essential tremor, a common movement disorder characterized mainly by a postural and kinetic tremor of the upper extremities. Twin and family history studies show a high heritability for essential tremor
Autor:
Karin Srulijes, Matthis Synofzik, Cornelia Schatton, Jochen Klenk, Clemens Becker, Lars Schwickert, Walter Maetzler
Publikováno v:
Neurodegenerative diseases 16(5-6), 317-323 (2016). doi:10.1159/000444802
Background and Purpose: Reduced ambulatory activity is a major burden in neurodegenerative disease (NDD), leading to severe restrictions in social participation and further deterioration of motor capacities. However, objective evidence on walking beh
Autor:
Stefanie, Lerche, Claudia, Schulte, Karin, Srulijes, Andrea, Pilotto, Tim W, Rattay, Ann-Kathrin, Hauser, Elke, Stransky, Christian, Deuschle, Ilona, Csoti, Ingolf, Lachmann, Henrik, Zetterberg, Inga, Liepelt-Scarfone, Thomas, Gasser, Walter, Maetzler, Daniela, Berg, Kathrin, Brockmann
Publikováno v:
Movement disorders 32(12), 1780-1783 (2017). doi:10.1002/mds.27199
A proportion of idiopathic Parkinson's disease patients (PDidiopathic ) with dementia show altered CSF profiles of amyloid β (Aβ) and Tau. PD patients with Glucocerebrosidase (GBA) mutations (PDGBA ) present with even more cognitive decline than se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::fbc63d1cae719a4241086b52bc672633
http://hdl.handle.net/11379/498935
http://hdl.handle.net/11379/498935