Showing results (421-430 of 553) with videos related to

Sort By:
Pageof 56
Human Brain Mapping|December 3, 2019
Longitudinal brain atrophy distribution in advanced Parkinson's disease: What makes the difference in "cognitive status" converters?Martin Gorges, Martin S Kunz, Hans-Peter Müller, et al.
Movement Disorders Clinical Practice|May 31, 2024
Anticipating Tomorrow: Tailoring Parkinson's Symptomatic Therapy Using Predictors of OutcomeRonald B Postuma, Daniel Weintraub, Tanya Simuni, et al.
Geroscience|August 7, 2026
Identification and phenotypic profiling of subgroups with distinct cognitive aging trajectoriesLydia M Federmann, Christian Mychajliw, Ulrike Sünkel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2017
Cognitive impairment in Glucocerebrosidase (GBA)-associated PD: Not primarily associated with cerebrospinal fluid Abeta and Tau profilesStefanie Lerche, Claudia Schulte, Karin Srulijes, et al.
Annals of Clinical and Translational Neurology|January 8, 2024
Aβ38 and Aβ43 do not differentiate between Alzheimer's disease and cerebral amyloid angiopathyJustina Dargvainiene, Ulf Jensen-Kondering, Benjamin Bender, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Enlarged hyperechogenic substantia nigra is related to motor performance and olfaction in the elderlyDaniela Berg, Klaus Seppi, Inga Liepelt, et al.
Human Molecular Genetics|June 18, 2005
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's diseaseKarsten M Strauss, L Miguel Martins, Helene Plun-Favreau, et al.
Frontiers in Aging Neuroscience|September 29, 2022
Walking parameters of older adults from a lower back inertial measurement unit, a 6-year longitudinal observational studyMorad Elshehabi, Silvia Del Din, Markus A Hobert, et al.
Scientific Data|December 10, 2015
Multi-omic profiles of human non-alcoholic fatty liver disease tissue highlight heterogenic phenotypesWasco Wruck, Karl Kashofer, Samrina Rehman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 13, 2019
Dementia with lewy bodies: GBA1 mutations are associated with cerebrospinal fluid alpha-synuclein profileStefanie Lerche, Gerrit Machetanz, Isabel Wurster, et al.
Pageof 56