Overview of TDP-43 Proteinopathies: Shared Mechanisms Underlying Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis, The F. E. Bennett Lecture

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Identifier Overview_of_TDP-43_Proteinopathies
Title Overview of TDP-43 Proteinopathies: Shared Mechanisms Underlying Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis, The F. E. Bennett Lecture
Creator John Q. Trojanowski, MD, PhD
Affiliation Professor of Pathology and Laboratory Medicine Co-Director, Center for Neurodegenerative Disease Research University of Pennsylvania
Subject Acquired Ocular Motor Apraxia; Acquired Oculomotor Apraxia; CNS Degeneration; Complete paralysis of voluntary horizontal saccades on command to look left; Frontotemporal Dementia; Impaired pursuit; Inability to make a refixation saccade on command to a target held on the left; Normal voluntary horizontal saccadic eye movements to the right; Picks Disease; Saccadic initiation deficit of unilateral horizontal gaze
Description Slideshow describing condition.
Date 2002
Language eng
Format application/pdf
Format Creation Microsoft PowerPoint
Type Text
Relation is Part of 925-3
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
Rights Management Copyright 2002. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6962rxb
Setname ehsl_novel_novel
ID 185486
Reference URL https://collections.lib.utah.edu/ark:/87278/s6962rxb
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