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Keith Josephs

Showing results (1-10 of 10) with videos related to

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Expert Review of Neurotherapeutics|June 15, 2018
The diagnosis of progressive supranuclear palsy: current opinions and challengesFarwa Ali, Keith Josephs
Seminars in Neurology|March 30, 2019
Rare TauopathiesFarwa Ali, Keith Josephs
Journal of Communication Disorders|August 6, 2014
The Apraxia of Speech Rating Scale: a tool for diagnosis and description of apraxia of speechEdythe A Strand, Joseph R Duffy, Heather M Clark, et al.
Mayo Clinic Proceedings|December 17, 2016
High School Football and Late-Life Risk of Neurodegenerative Syndromes, 1956-1970Pieter H H Janssen, Jay Mandrekar, Michelle M Mielke, et al.
Neuromuscular Disorders : NMD|July 1, 2008
Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutationsMargherita Milone, Nicola Brunetti-Pierri, Lin-Ya Tang, et al.
Neuroscience Letters|January 25, 2006
CHMP2B mutations are not a common cause of frontotemporal lobar degenerationAshley Cannon, Matthew Baker, Brad Boeve, et al.
Alzheimer Disease and Associated Disorders|December 20, 2007
Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directionsKatya Rascovsky, John R Hodges, Christopher M Kipps, et al.
Brain : a Journal of Neurology|October 23, 2020
Predicting future rates of tau accumulation on PETClifford R Jack, Heather J Wiste, Stephen D Weigand, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Expert Review of Neurotherapeutics|June 15, 2018
The diagnosis of progressive supranuclear palsy: current opinions and challengesFarwa Ali, Keith Josephs
Seminars in Neurology|March 30, 2019
Rare TauopathiesFarwa Ali, Keith Josephs
Journal of Communication Disorders|August 6, 2014
The Apraxia of Speech Rating Scale: a tool for diagnosis and description of apraxia of speechEdythe A Strand, Joseph R Duffy, Heather M Clark, et al.
Mayo Clinic Proceedings|December 17, 2016
High School Football and Late-Life Risk of Neurodegenerative Syndromes, 1956-1970Pieter H H Janssen, Jay Mandrekar, Michelle M Mielke, et al.
Neuromuscular Disorders : NMD|July 1, 2008
Sensory ataxic neuropathy with ophthalmoparesis caused by POLG mutationsMargherita Milone, Nicola Brunetti-Pierri, Lin-Ya Tang, et al.
Neuroscience Letters|January 25, 2006
CHMP2B mutations are not a common cause of frontotemporal lobar degenerationAshley Cannon, Matthew Baker, Brad Boeve, et al.
Alzheimer Disease and Associated Disorders|December 20, 2007
Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directionsKatya Rascovsky, John R Hodges, Christopher M Kipps, et al.
Brain : a Journal of Neurology|October 23, 2020
Predicting future rates of tau accumulation on PETClifford R Jack, Heather J Wiste, Stephen D Weigand, et al.
Human Molecular Genetics|September 5, 2006
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degenerationJennifer Gass, Ashley Cannon, Ian R Mackenzie, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Pageof 1