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Yujiro Higuchi

Showing results (101-110 of 154) with videos related to

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Internal Medicine (Tokyo, Japan)|July 5, 2023
Spatial Fluctuation of Central Nervous System Lesions in X-linked Charcot-Marie-Tooth Disease with a Novel GJB1 MutationYukiyo Yoshimoto, Shoko Yoshimoto, Kensuke Kakiuchi, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|March 14, 2026
Mid-term systolic BP variability beyond 24 h after successful recanalization predicts poor outcomes following ischemic strokeYuki Hamada, Hideki Matsuoka, Takeo Sato, et al.
Scientific Reports|February 14, 2020
Author Correction: Identification and characterization of a novel β-D-galactosidase that releases pyruvylated galactoseYujiro Higuchi, Hitomi Matsufuji, Masanari Tanuma, et al.
International Journal of Molecular Sciences|February 13, 2026
Functional and Epigenomic Consequences of <i>DNMT1</i> Variants in Inherited Neurological DisordersJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Brain & Development|September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illnessNoriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Multiple Sclerosis and Related Disorders|April 2, 2025
Visual evoked potential in myelin oligodendrocyte glycoprotein antibody-associated diseaseChikashi Yano, Eiji Matsuura, Tomonori Nakamura, et al.
Journal of Human Genetics|December 8, 2025
Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletionJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Frontiers in Neurology|September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Neuromuscular Disorders : NMD|May 25, 2019
PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variabilityToshitaka Kawarai, Hiroki Yamazaki, Ryosuke Miyamoto, et al.
Internal Medicine (Tokyo, Japan)|July 18, 2014
Partial deficiency of emerin caused by a splice site mutation in EMDJunhui Yuan, Masahiro Ando, Itsuro Higuchi, et al.
Pageof 16

Showing results (101-110 of 154) with videos related to

Sort By:
Pageof 16
Internal Medicine (Tokyo, Japan)|July 5, 2023
Spatial Fluctuation of Central Nervous System Lesions in X-linked Charcot-Marie-Tooth Disease with a Novel GJB1 MutationYukiyo Yoshimoto, Shoko Yoshimoto, Kensuke Kakiuchi, et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension|March 14, 2026
Mid-term systolic BP variability beyond 24 h after successful recanalization predicts poor outcomes following ischemic strokeYuki Hamada, Hideki Matsuoka, Takeo Sato, et al.
Scientific Reports|February 14, 2020
Author Correction: Identification and characterization of a novel β-D-galactosidase that releases pyruvylated galactoseYujiro Higuchi, Hitomi Matsufuji, Masanari Tanuma, et al.
International Journal of Molecular Sciences|February 13, 2026
Functional and Epigenomic Consequences of <i>DNMT1</i> Variants in Inherited Neurological DisordersJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Brain & Development|September 5, 2018
X-linked Charcot-Marie-Tooth disease type 5 with recurrent weakness after febrile illnessNoriko Nishikura, Takanori Yamagata, Takao Morimune, et al.
Multiple Sclerosis and Related Disorders|April 2, 2025
Visual evoked potential in myelin oligodendrocyte glycoprotein antibody-associated diseaseChikashi Yano, Eiji Matsuura, Tomonori Nakamura, et al.
Journal of Human Genetics|December 8, 2025
Respiratory complex I deficiency caused by a novel multi-exonic PUS1 deletionJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Frontiers in Neurology|September 5, 2022
Multi-type <i>RFC1</i> repeat expansions as the most common cause of hereditary sensory and autonomic neuropathyJun-Hui Yuan, Yujiro Higuchi, Masahiro Ando, et al.
Neuromuscular Disorders : NMD|May 25, 2019
PMP22-related disease: A novel splice site acceptor variant and intrafamilial phenotype variabilityToshitaka Kawarai, Hiroki Yamazaki, Ryosuke Miyamoto, et al.
Internal Medicine (Tokyo, Japan)|July 18, 2014
Partial deficiency of emerin caused by a splice site mutation in EMDJunhui Yuan, Masahiro Ando, Itsuro Higuchi, et al.
Pageof 16