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Norikazu Hara

Showing results (1-10 of 64) with videos related to

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Brain and Nerve = Shinkei Kenkyu No Shinpo|March 12, 2013
[Personal genomics for Alzheimer's disease]Ryozo Kuwano, Norikazu Hara
Brain and Nerve = Shinkei Kenkyu No Shinpo|October 8, 2019
[Genetic Analysis of Alzheimer's Disease: The Impact of Rare Variants and Their Significance]Akinori Miyashita, Lixin Liu, Norikazu Hara
Journal of Human Genetics|May 31, 2022
Genetics of Alzheimer's disease: an East Asian perspectiveAkinori Miyashita, Masataka Kikuchi, Norikazu Hara, et al.
Brain and Nerve = Shinkei Kenkyu No Shinpo|July 11, 2016
[Multifunctional Roles of APOE in Alzheimer's Disease Pathogenesis]Takayoshi Tokutake, Kensaku Kasuga, Norikazu Hara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2024
An early-onset case of adult-onset autosomal dominant leukodystrophyIzumi Mihashi, Kazuhiro Ishii, Norikazu Hara, et al.
BMC Medical Genomics|September 11, 2019
Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin loopingMasataka Kikuchi, Norikazu Hara, Mai Hasegawa, et al.
Internal Medicine (Tokyo, Japan)|March 9, 2025
Inherited Prion Disease with a 5-octapeptide Repeat Insertion in the PRNP Gene Presenting with Familial Juvenile Dementia: A Case ReportMasafumi Nishikawa, Akitoshi Takeda, Naotaka Miyazawa, et al.
Geriatrics & Gerontology International|February 24, 2022
Focal striatal amyloid deposition in Alzheimer's disease caused by APP p.V717I mutation: Longitudinal positron emission tomography studyRyota Kobayashi, Shinobu Kawakatsu, Hiroshi Hayashi, et al.
Journal of Alzheimer'S Disease Reports|April 3, 2026
A novel <i>PSEN2</i> missense variant in a Japanese woman with hereditary Alzheimer's diseaseKazuki Kasuga, Chinami Yuzawa, Katsuya Nakamura, et al.
Journal of the Neurological Sciences|December 27, 2016
Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a familyArika Hasegawa, Ryoko Koike, Kishin Koh, et al.
Pageof 7

Showing results (1-10 of 64) with videos related to

Sort By:
Pageof 7
Brain and Nerve = Shinkei Kenkyu No Shinpo|March 12, 2013
[Personal genomics for Alzheimer's disease]Ryozo Kuwano, Norikazu Hara
Brain and Nerve = Shinkei Kenkyu No Shinpo|October 8, 2019
[Genetic Analysis of Alzheimer's Disease: The Impact of Rare Variants and Their Significance]Akinori Miyashita, Lixin Liu, Norikazu Hara
Journal of Human Genetics|May 31, 2022
Genetics of Alzheimer's disease: an East Asian perspectiveAkinori Miyashita, Masataka Kikuchi, Norikazu Hara, et al.
Brain and Nerve = Shinkei Kenkyu No Shinpo|July 11, 2016
[Multifunctional Roles of APOE in Alzheimer's Disease Pathogenesis]Takayoshi Tokutake, Kensaku Kasuga, Norikazu Hara, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 24, 2024
An early-onset case of adult-onset autosomal dominant leukodystrophyIzumi Mihashi, Kazuhiro Ishii, Norikazu Hara, et al.
BMC Medical Genomics|September 11, 2019
Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin loopingMasataka Kikuchi, Norikazu Hara, Mai Hasegawa, et al.
Internal Medicine (Tokyo, Japan)|March 9, 2025
Inherited Prion Disease with a 5-octapeptide Repeat Insertion in the PRNP Gene Presenting with Familial Juvenile Dementia: A Case ReportMasafumi Nishikawa, Akitoshi Takeda, Naotaka Miyazawa, et al.
Geriatrics & Gerontology International|February 24, 2022
Focal striatal amyloid deposition in Alzheimer's disease caused by APP p.V717I mutation: Longitudinal positron emission tomography studyRyota Kobayashi, Shinobu Kawakatsu, Hiroshi Hayashi, et al.
Journal of Alzheimer'S Disease Reports|April 3, 2026
A novel <i>PSEN2</i> missense variant in a Japanese woman with hereditary Alzheimer's diseaseKazuki Kasuga, Chinami Yuzawa, Katsuya Nakamura, et al.
Journal of the Neurological Sciences|December 27, 2016
Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a familyArika Hasegawa, Ryoko Koike, Kishin Koh, et al.
Pageof 7