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Yujiro Higuchi

Showing results (141-150 of 154) with videos related to

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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.
Journal of Neurology|July 16, 2025
Charcot-Marie-Tooth-like presentation in giant axonal neuropathy: clinical variability and prevalence in a large Japanese case seriesTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Journal of the Peripheral Nervous System : JPNS|January 31, 2018
Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in JapanHajime Tanabe, Yujiro Higuchi, Jun-Hui Yuan, et al.
Journal of Neurology|March 2, 2022
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genesYu Hiramatsu, Yuji Okamoto, Akiko Yoshimura, et al.
Brain Communications|May 9, 2025
Brain biopsy and metagenomic sequencing enhance aetiological diagnosis of encephalitisYusuke Sakiyama, Jun-Hui Yuan, Akiko Yoshimura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2026
Biallelic variants in FAT3 cause axonal neuropathy with multisystem neurodevelopmental featuresYujiro Higuchi, Kaichi Yoshizaki, Kazuki Nakanishi, et al.
Annals of Clinical and Translational Neurology|September 23, 2025
INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical InsightsChikashi Yano, Masahiro Ando, Yujiro Higuchi, et al.
Scientific Reports|April 9, 2026
Asthma-like bronchodilator responsiveness in patients with neuronal intranuclear inclusion diseaseDaisuke Tahara, Nao Tahara, Chisato Tamai, et al.
Brain : a Journal of Neurology|May 3, 2018
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathyYujiro Higuchi, Ryuta Okunushi, Taichi Hara, et al.
Pageof 16

Showing results (141-150 of 154) with videos related to

Sort By:
Pageof 16
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.
Journal of Neurology|July 16, 2025
Charcot-Marie-Tooth-like presentation in giant axonal neuropathy: clinical variability and prevalence in a large Japanese case seriesTakahiro Hobara, Masahiro Ando, Yujiro Higuchi, et al.
Journal of the Peripheral Nervous System : JPNS|January 31, 2018
Clinical and genetic features of Charcot-Marie-Tooth disease 2F and hereditary motor neuropathy 2B in JapanHajime Tanabe, Yujiro Higuchi, Jun-Hui Yuan, et al.
Journal of Neurology|March 2, 2022
Complex hereditary peripheral neuropathies caused by novel variants in mitochondrial-related nuclear genesYu Hiramatsu, Yuji Okamoto, Akiko Yoshimura, et al.
Brain Communications|May 9, 2025
Brain biopsy and metagenomic sequencing enhance aetiological diagnosis of encephalitisYusuke Sakiyama, Jun-Hui Yuan, Akiko Yoshimura, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2026
Biallelic variants in FAT3 cause axonal neuropathy with multisystem neurodevelopmental featuresYujiro Higuchi, Kaichi Yoshizaki, Kazuki Nakanishi, et al.
Annals of Clinical and Translational Neurology|September 23, 2025
INF2-Related Charcot-Marie-Tooth Disease in a Japanese Cohort: Genetic and Clinical InsightsChikashi Yano, Masahiro Ando, Yujiro Higuchi, et al.
Scientific Reports|April 9, 2026
Asthma-like bronchodilator responsiveness in patients with neuronal intranuclear inclusion diseaseDaisuke Tahara, Nao Tahara, Chisato Tamai, et al.
Brain : a Journal of Neurology|May 3, 2018
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathyYujiro Higuchi, Ryuta Okunushi, Taichi Hara, et al.
Pageof 16