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Journal of Intellectual & Developmental Disability|January 16, 2025
Measurement properties of the German version of the Cambridge examination for mental disorders of older people with Down syndrome and others with intellectual disabilities (CAMDEX-DS)Sandra V Loosli, Lennart C Neumann, Elisabeth Wlasich, et al.Journal of Alzheimer'S Disease : JAD|August 4, 2020
Frontal Pole Hypometabolism Linked to Reduced Prosocial Sexual Behaviors in Frontotemporal Dementia and Corticobasal SyndromeHannah E Silverman, Yunglin Gazes, Megan S Barker, et al.Journal of Neurology|July 6, 2015
The association of aphasia and right-sided motor impairment in corticobasal syndromeJohannes Levin, Thomas H Bak, Axel Rominger, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 26, 2013
Atypical parkinsonism due to a D202N Gerstmann-Sträussler-Scheinker prion protein mutation: first in vivo diagnosed caseAnnika Plate, Jens Benninghoff, Gerald H Jansen, et al.Brain Communications|April 25, 2020
Brain phenotyping in Moebius syndrome and other congenital facial weakness disorders by diffusion MRI morphometryNeda Sadeghi, Elizabeth Hutchinson, Carol Van Ryzin, et al.Antioxidants (Basel, Switzerland)|January 21, 2022
Adaptative Up-Regulation of PRX2 and PRX5 Expression Characterizes Brain from a Mouse Model of Chorea-AcanthocytosisEnrica Federti, Alessandro Matte, Veronica Riccardi, et al.BMC Neurology|December 30, 2022
Limits on using the clock drawing test as a measure to evaluate patients with neurological disordersRaheleh Heyrani, Atiye Sarabi-Jamab, Jordan Grafman, et al.Psychiatry Research|March 8, 2011
Shape alterations in the striatum in chorea-acanthocytosisMark Walterfang, Jeffrey Chee Leong Looi, Martin Styner, et al.Science Translational Medicine|December 16, 2016
Early changes in CSF sTREM2 in dominantly inherited Alzheimer's disease occur after amyloid deposition and neuronal injuryMarc Suárez-Calvet, Miguel Ángel Araque Caballero, Gernot Kleinberger, et al.Human Mutation|August 29, 2019
A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)Dror Sharon, Tamar Ben-Yosef, Nitza Goldenberg-Cohen, et al.Pageof 58