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Akihiro Hashiguchi

Showing results (81-90 of 101) with videos related to

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Annals of Clinical and Translational Neurology|December 22, 2022
Efficacy of l-Arginine treatment in patients with HTLV-1-associated neurological diseaseSatoshi Nozuma, Eiji Matsuura, Yuichi Tashiro, et al.
Neuropathology and Applied Neurobiology|September 5, 2014
Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutationSatoshi Yamashita, Akira Mori, Yasuto Nishida, et al.
Frontiers in Neurology|August 29, 2022
Genetic and clinical features of cerebellar ataxia with <i>RFC1</i> biallelic repeat expansions in JapanMasahiro Ando, Yujiro Higuchi, Junhui H Yuan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 22, 2023
Clinical phenotypic diversity of <i>NOTCH2NLC</i>-related disease in the largest case series of inherited peripheral neuropathy in JapanMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 16, 2024
Linking LRP12 CGG repeat expansion to inherited peripheral neuropathyTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Journal of Human Genetics|January 14, 2022
Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatmentsTakaki Taniguchi, Masahiro Ando, Yuji Okamoto, et al.
Journal of Human Genetics|January 29, 2022
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese familiesMasahiro Ando, Yujiro Higuchi, Yuji Okamoto, et al.
Annals of Clinical and Translational Neurology|November 2, 2023
Clinical variability associated with intronic FGF14 GAA repeat expansion in JapanMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Journal of the Peripheral Nervous System : JPNS|August 9, 2023
Genetic, electrophysiological, and pathological studies on patients with SCN9A-related pain disordersJun-Hui Yuan, Xiaoyang Cheng, Eiji Matsuura, et al.
Annals of Clinical and Translational Neurology|June 23, 2022
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth diseaseMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Pageof 11

Showing results (81-90 of 101) with videos related to

Sort By:
Pageof 11
Annals of Clinical and Translational Neurology|December 22, 2022
Efficacy of l-Arginine treatment in patients with HTLV-1-associated neurological diseaseSatoshi Nozuma, Eiji Matsuura, Yuichi Tashiro, et al.
Neuropathology and Applied Neurobiology|September 5, 2014
Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutationSatoshi Yamashita, Akira Mori, Yasuto Nishida, et al.
Frontiers in Neurology|August 29, 2022
Genetic and clinical features of cerebellar ataxia with <i>RFC1</i> biallelic repeat expansions in JapanMasahiro Ando, Yujiro Higuchi, Junhui H Yuan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 22, 2023
Clinical phenotypic diversity of <i>NOTCH2NLC</i>-related disease in the largest case series of inherited peripheral neuropathy in JapanMasahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 16, 2024
Linking LRP12 CGG repeat expansion to inherited peripheral neuropathyTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Journal of Human Genetics|January 14, 2022
Elderly patients with suspected Charcot-Marie-Tooth disease should be tested for the TTR gene for effective treatmentsTakaki Taniguchi, Masahiro Ando, Yuji Okamoto, et al.
Journal of Human Genetics|January 29, 2022
An NEFH founder mutation causes broad phenotypic spectrum in multiple Japanese familiesMasahiro Ando, Yujiro Higuchi, Yuji Okamoto, et al.
Annals of Clinical and Translational Neurology|November 2, 2023
Clinical variability associated with intronic FGF14 GAA repeat expansion in JapanMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Journal of the Peripheral Nervous System : JPNS|August 9, 2023
Genetic, electrophysiological, and pathological studies on patients with SCN9A-related pain disordersJun-Hui Yuan, Xiaoyang Cheng, Eiji Matsuura, et al.
Annals of Clinical and Translational Neurology|June 23, 2022
Novel heterozygous variants of SLC12A6 in Japanese families with Charcot-Marie-Tooth diseaseMasahiro Ando, Yujiro Higuchi, Junhui Yuan, et al.
Pageof 11