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Elsdon Storey

Showing results (81-90 of 154) with videos related to

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Annals of the New York Academy of Sciences|September 29, 2011
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosisDavid J Szmulewicz, John A Waterston, Hamish G MacDougall, et al.
Psychology and Aging|November 30, 2011
Knowledge and use of memory strategies in amnestic mild cognitive impairmentRachel L Hutchens, Glynda J Kinsella, Ben Ong, et al.
Molecular Genetics & Genomic Medicine|November 26, 2024
Parkinson's Disease Polygenic Risk Score and Neurological Involvement in Carriers of the FMR1 Premutation Allele: A Case for Genetic ModifierDanuta Z Loesch, Freddy Chafota, Minh Q Bui, et al.
Frontiers in Neurology|August 22, 2022
Potential modifiable factors associated with late-life cognitive trajectoriesZimu Wu, Robyn L Woods, Trevor T-J Chong, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 10, 2021
Trajectories of cognitive function in community-dwelling older adults: A longitudinal study of population heterogeneityZimu Wu, Robyn L Woods, Rory Wolfe, et al.
Journal of Neurology|July 4, 2018
Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
BMC Neurology|February 10, 2012
Aspirin for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion)Christopher M Reid, Elsdon Storey, Tien Y Wong, et al.
Clinical Chemistry|May 9, 2009
Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15Devika Ganesamoorthy, Damien L Bruno, Jacqueline Schoumans, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Pageof 16

Showing results (81-90 of 154) with videos related to

Sort By:
Pageof 16
Annals of the New York Academy of Sciences|September 29, 2011
Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS): a review of the clinical features and video-oculographic diagnosisDavid J Szmulewicz, John A Waterston, Hamish G MacDougall, et al.
Psychology and Aging|November 30, 2011
Knowledge and use of memory strategies in amnestic mild cognitive impairmentRachel L Hutchens, Glynda J Kinsella, Ben Ong, et al.
Molecular Genetics & Genomic Medicine|November 26, 2024
Parkinson's Disease Polygenic Risk Score and Neurological Involvement in Carriers of the FMR1 Premutation Allele: A Case for Genetic ModifierDanuta Z Loesch, Freddy Chafota, Minh Q Bui, et al.
Frontiers in Neurology|August 22, 2022
Potential modifiable factors associated with late-life cognitive trajectoriesZimu Wu, Robyn L Woods, Trevor T-J Chong, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 10, 2021
Trajectories of cognitive function in community-dwelling older adults: A longitudinal study of population heterogeneityZimu Wu, Robyn L Woods, Rory Wolfe, et al.
Journal of Neurology|July 4, 2018
Coordination and timing deficits in speech and swallowing in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)Adam P Vogel, Natalie Rommel, Andreas Oettinger, et al.
Neuroepidemiology|June 7, 2003
A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosisHatice Aksoy, Geoffrey Dean, Marta Elian, et al.
BMC Neurology|February 10, 2012
Aspirin for the prevention of cognitive decline in the elderly: rationale and design of a neuro-vascular imaging study (ENVIS-ion)Christopher M Reid, Elsdon Storey, Tien Y Wong, et al.
Clinical Chemistry|May 9, 2009
Development of a multiplex ligation-dependent probe amplification assay for diagnosis and estimation of the frequency of spinocerebellar ataxia type 15Devika Ganesamoorthy, Damien L Bruno, Jacqueline Schoumans, et al.
Neurology. Genetics|October 30, 2016
Heterozygous mutations in <i>HSD17B4</i> cause juvenile peroxisomal D-bifunctional protein deficiencyDavid J Amor, Ashley P L Marsh, Elsdon Storey, et al.
Pageof 16