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L WALTON

Showing results (461-470 of 517) with videos related to

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Science Advances|August 16, 2024
The source craters of the martian meteorites: Implications for the igneous evolution of MarsChristopher D K Herd, Jarret S Hamilton, Erin L Walton, et al.
Parkinsonism & Related Disorders|July 6, 2020
GBA variation and susceptibility to multiple system atrophyAnna I Wernick, Ronald L Walton, Shunsuke Koga, et al.
Mitochondrion|August 23, 2024
Associations of mitochondrial genomic variation with successful neurological agingNicole Tamvaka, Michael G Heckman, Patrick W Johnson, et al.
Parkinsonism & Related Disorders|January 17, 2021
Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's diseaseMichael G Heckman, Catherine Labbé, Ana L Kolicheski, et al.
Studies in Health Technology and Informatics|May 21, 2015
iCarer: AAL for the Informal Carers of the ElderlyP A Moreno, J L Garcia-Pacheco, J Charvill, et al.
Acta Neuropathologica|June 22, 2018
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtypeShunsuke Koga, Naomi Kouri, Ronald L Walton, et al.
Neuroscience Letters|February 18, 2021
Investigating ELOVL7 coding variants in multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2016
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degenerationMonica Sanchez-Contreras, Michael G Heckman, Pawel Tacik, et al.
Acta Neuropathologica|November 1, 2015
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bankKevin F Bieniek, Owen A Ross, Kerry A Cormier, et al.
Parkinsonism & Related Disorders|August 24, 2020
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's diseaseAlexandra I Soto-Beasley, Ronald L Walton, Rebecca R Valentino, et al.
Pageof 52

Showing results (461-470 of 517) with videos related to

Sort By:
Pageof 52
Science Advances|August 16, 2024
The source craters of the martian meteorites: Implications for the igneous evolution of MarsChristopher D K Herd, Jarret S Hamilton, Erin L Walton, et al.
Parkinsonism & Related Disorders|July 6, 2020
GBA variation and susceptibility to multiple system atrophyAnna I Wernick, Ronald L Walton, Shunsuke Koga, et al.
Mitochondrion|August 23, 2024
Associations of mitochondrial genomic variation with successful neurological agingNicole Tamvaka, Michael G Heckman, Patrick W Johnson, et al.
Parkinsonism & Related Disorders|January 17, 2021
Fine-mapping of the non-coding variation driving the Caucasian LRRK2 GWAS signal in Parkinson's diseaseMichael G Heckman, Catherine Labbé, Ana L Kolicheski, et al.
Studies in Health Technology and Informatics|May 21, 2015
iCarer: AAL for the Informal Carers of the ElderlyP A Moreno, J L Garcia-Pacheco, J Charvill, et al.
Acta Neuropathologica|June 22, 2018
Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtypeShunsuke Koga, Naomi Kouri, Ronald L Walton, et al.
Neuroscience Letters|February 18, 2021
Investigating ELOVL7 coding variants in multiple system atrophyAnna I Wernick, Ronald L Walton, Alexandra I Soto-Beasley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2016
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degenerationMonica Sanchez-Contreras, Michael G Heckman, Pawel Tacik, et al.
Acta Neuropathologica|November 1, 2015
Chronic traumatic encephalopathy pathology in a neurodegenerative disorders brain bankKevin F Bieniek, Owen A Ross, Kerry A Cormier, et al.
Parkinsonism & Related Disorders|August 24, 2020
Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's diseaseAlexandra I Soto-Beasley, Ronald L Walton, Rebecca R Valentino, et al.
Pageof 52