Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Simone Van De Loo"'
Autor:
Karin Wirdefeldt, Brian K. Fiske, Chin-Hsien Lin, Jessie Theuns, Young H. Sohn, Nadine Abahuni, Simone Van De Loo, Vera Tadic, Jonathan Carr, John P. A. Ioannidis, Simona Petrucci, Jan O. Aasly, Grazia Annesi, Matthew J. Farrer, Hiroyuki Tomiyama, Demetrius M. Maraganore, Suzanne Lesage, Sung Sup Park, Magdalena Boczarska-Jedynak, Zbigniew K. Wszolek, Dennis W. Dickson, Elli Kyratzi, Peter A. Silburn, Nancy N. Diehl, Alexis Brice, Leonidas Stefanis, Enza Maria Valente, Marie-Christine Chartier-Harlin, J. Mark Gibson, Ruey-Meei Wu, Christine Klein, Nobutaka Hattori, Andreas Puschmann, George D. Mellick, Georgios M. Hadjigeorgiou, Alexandra I. Soto-Ortolaza, Beom S. Jeon, Aldo Quattrone, Christine Van Broeckhoven, Efthimios Dardiotis, Demetrios K. Vassilatis, Laura Brighina, Maria Bozi, Yun Joong Kim, Christer Nilsson, Justin A. Bacon, Ryan J. Uitti, Eugénie Mutez, Soraya Bardien, Carles Vilariño-Güell, Michael G. Heckman, Rejko Krüger, Manu Sharma, Rachel A. Gibson, Timothy Lynch, Linda R. White, Barbara Jasinska-Myga, Fayçal Hentati, Carlo Ferrarese, Grzegorz Opala, Owen A. Ross, Alexis Elbaz
Publikováno v:
Movement Disorders. 28:1740-1744
BackgroundVariants within the leucine-rich repeat kinase 2 gene are recognized as the most frequent genetic cause of Parkinson's disease. Leucine-rich repeat kinase 2 variation related to disease susceptibility displays many features that reflect the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecfdc887c7af5e9fa70021227ff3ad13
https://doi.org/10.1002/mds.25600
https://doi.org/10.1002/mds.25600
Autor:
Andrea Szelényi, Rainer Hartmann, Lutz Weise, Volker Seifert, Jochen Roeper, Carola Seifried, Thomas Gasser, Simon Baudrexel, Rüdiger Hilker, Simone van de Loo, Helmuth Steinmetz
Publikováno v:
Brain Stimulation, Vol 5, Iss 3, Pp 378-387 (2012)
Background: The subthalamic nucleus (STN) as an effective target for deep brain stimulation (DBS) in advanced Parkinson’s disease is functionally divided into the dorsolateral sensorimotor and the ventromedial limbic and associative parts. To impla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61608d483c93fdaf3e852706877acf5c
https://pubmed.ncbi.nlm.nih.gov/21782543
https://pubmed.ncbi.nlm.nih.gov/21782543
Autor:
Carola Seifried, Simone van de Loo, Johannes C. Klein, Helmuth Steinmetz, Ralph Deichmann, Simon Baudrexel, Jun-Suk Kang, Rüdiger Hilker, Benedikt Lorenz
Publikováno v:
Hum Brain Mapp
This study set out to determine whether there is white matter involvement in essential tremor (ET), the most common movement disorder. We collected diffusion MRI and analysed differences in fractional anisotropy (FA) and mean diffusivity (MD) between
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d6386d1a751409278f47d8299338dfe
https://europepmc.org/articles/PMC6870356/
https://europepmc.org/articles/PMC6870356/
Autor:
Simone van de Loo, Matthias W. Lorenz, Stefanie Behnke, Johann Hagenah, Daniela Berg, Rüdiger Hilker, Matthias Sitzer, Uwe Walter
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 81(10)
Objective Transcranial sonography (TCS) shows characteristic hyperechogenicity of the substantia nigra (SN) in patients with Parkinson9s disease (PD). Although this feature is well established, sufficient observer reliability and diagnostic accuracy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56f46359404c74311337c64970097306
https://pubmed.ncbi.nlm.nih.gov/20543186
https://pubmed.ncbi.nlm.nih.gov/20543186
Publikováno v:
Experimental neurology. 215(1)
Ataxin-2 is a novel protein, normally with a domain of 22 consecutive glutamine (Q) residues, which may expand beyond a threshold of (Q)(32), causing a neurodegenerative disease named Spinocerebellar ataxia type 2 (SCA2). To obtain clues about the fu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eec64eace571d3ff77a05f39a98dc895
https://pubmed.ncbi.nlm.nih.gov/18973756
https://pubmed.ncbi.nlm.nih.gov/18973756
Autor:
Simone van de Loo, Florian Eich, Ivan Dikic, Mirko H. H. Schmidt, Georg Auburger, David Nonis, Joachim Nowock
Publikováno v:
Cellular signalling. 20(10)
Ataxin-2 is a novel protein, where the unstable expansion of an internal polyglutamine domain can cause the neurodegenerative disease Spinocerebellar Ataxia type 2 (SCA2). To elucidate its cellular function, we have used full-length ataxin-2 as bait
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc45bf6ba06df0270ead73304cd3716f
https://pubmed.ncbi.nlm.nih.gov/18602463
https://pubmed.ncbi.nlm.nih.gov/18602463
Autor:
Rüdiger Hilker, Sriramya Somasundaram, Marlies Wagner, Simone van de Loo, Helmuth Steinmetz, Oliver C. Singer
Publikováno v:
Movement Disorders. 25:1304-1305
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82da0f1d4e696d6af0b312bcdb0f1a02
https://doi.org/10.1002/mds.23076
https://doi.org/10.1002/mds.23076