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L WALTON

Showing results (501-510 of 517) with videos related to

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Neurobiology of Aging|July 28, 2016
RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodiesKyndall Hodges, Sheridan S Brewer, Catherine Labbé, et al.
Parkinsonism & Related Disorders|April 12, 2021
Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central EuropeŁukasz M Milanowski, Jennifer A Lindemann, Dorota Hoffman-Zacharska, et al.
Scientific Reports|September 8, 2018
The 2015 landslide and tsunami in Taan Fiord, AlaskaBretwood Higman, Dan H Shugar, Colin P Stark, et al.
Molecular Neurodegeneration|October 18, 2018
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African AmericansOlivia J Conway, Minerva M Carrasquillo, Xue Wang, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
European Journal of Neurology|August 18, 2015
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patientsO Lorenzo-Betancor, K Ogaki, A I Soto-Ortolaza, et al.
Neurology|November 13, 2015
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disordersKotaro Ogaki, Shunsuke Koga, Michael G Heckman, et al.
Acta Neuropathologica|March 13, 2024
Role of GBA variants in Lewy body disease neuropathologyRonald L Walton, Shunsuke Koga, Alexandra I Beasley, et al.
Acta Neuropathologica Communications|July 14, 2022
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measuresRebecca R Valentino, Chloe Ramnarine, Michael G Heckman, et al.
International Journal of Molecular Sciences|July 9, 2022
Cathepsin B p.Gly284Val Variant in Parkinson's Disease PathogenesisLukasz M Milanowski, Xu Hou, Jenny M Bredenberg, et al.
Pageof 52

Showing results (501-510 of 517) with videos related to

Sort By:
Pageof 52
Neurobiology of Aging|July 28, 2016
RAB39B gene mutations are not a common cause of Parkinson's disease or dementia with Lewy bodiesKyndall Hodges, Sheridan S Brewer, Catherine Labbé, et al.
Parkinsonism & Related Disorders|April 12, 2021
Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central EuropeŁukasz M Milanowski, Jennifer A Lindemann, Dorota Hoffman-Zacharska, et al.
Scientific Reports|September 8, 2018
The 2015 landslide and tsunami in Taan Fiord, AlaskaBretwood Higman, Dan H Shugar, Colin P Stark, et al.
Molecular Neurodegeneration|October 18, 2018
ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African AmericansOlivia J Conway, Minerva M Carrasquillo, Xue Wang, et al.
Neurology. Genetics|July 27, 2016
TREM2 p.R47H substitution is not associated with dementia with Lewy bodiesRonald L Walton, Alexandra I Soto-Ortolaza, Melissa E Murray, et al.
European Journal of Neurology|August 18, 2015
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patientsO Lorenzo-Betancor, K Ogaki, A I Soto-Ortolaza, et al.
Neurology|November 13, 2015
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disordersKotaro Ogaki, Shunsuke Koga, Michael G Heckman, et al.
Acta Neuropathologica|March 13, 2024
Role of GBA variants in Lewy body disease neuropathologyRonald L Walton, Shunsuke Koga, Alexandra I Beasley, et al.
Acta Neuropathologica Communications|July 14, 2022
Mitochondrial genomic variation in dementia with Lewy bodies: association with disease risk and neuropathological measuresRebecca R Valentino, Chloe Ramnarine, Michael G Heckman, et al.
International Journal of Molecular Sciences|July 9, 2022
Cathepsin B p.Gly284Val Variant in Parkinson's Disease PathogenesisLukasz M Milanowski, Xu Hou, Jenny M Bredenberg, et al.
Pageof 52