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Jun Mitsui

Showing results (31-40 of 183) with videos related to

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Journal of Clinical Medicine|September 14, 2024
Esophageal Dysmotility in Multiple System Atrophy: A Retrospective Cross-Sectional StudyRumi Ueha, Misaki Koyama, Akiko Seto, et al.
Journal of the Neurological Sciences|December 19, 2017
A Japanese family with mutation in the proteinase inhibitor 12 L47P gene: A case reportHaruka Amano-Takeshige, Genko Oyama, Kazuaki Kanai, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 24, 2004
[A case of chronic inflammatory demyelinating polyneuropathy presenting with acute pain and SIADH followed by weakness of all four limbs 2 month after the first symptoms]Jun Mitsui, Izumi Sugimoto, Satoko Kano, et al.
Journal of Human Genetics|June 20, 2018
Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairmentKishin Koh, Hiroyuki Ishiura, Minako Beppu, et al.
Parkinsonism & Related Disorders|January 18, 2015
The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN geneKazumasa Saigoh, Jun Mitsui, Makito Hirano, et al.
The Laryngoscope|July 5, 2020
Esophageal Dysmotility is Common in Patients With Multiple System AtrophyRumi Ueha, Taku Sato, Takao Goto, et al.
Internal Medicine (Tokyo, Japan)|December 12, 2017
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese PatientAkatsuki Kubota, Hiroyuki Ishiura, Jun Mitsui, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2023
Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1Hiroya Naruse, So Okubo, Atsushi Sudo, et al.
Cerebellum (London, England)|November 30, 2021
Frequency of FMR1 Premutation Alleles in Patients with Undiagnosed Cerebellar Ataxia and Multiple System Atrophy in the Japanese PopulationAsem Almansour, Hiroyuki Ishiura, Jun Mitsui, et al.
Pageof 19

Showing results (31-40 of 183) with videos related to

Sort By:
Pageof 19
Journal of Clinical Medicine|September 14, 2024
Esophageal Dysmotility in Multiple System Atrophy: A Retrospective Cross-Sectional StudyRumi Ueha, Misaki Koyama, Akiko Seto, et al.
Journal of the Neurological Sciences|December 19, 2017
A Japanese family with mutation in the proteinase inhibitor 12 L47P gene: A case reportHaruka Amano-Takeshige, Genko Oyama, Kazuaki Kanai, et al.
Neurogenetics|March 9, 2019
Association of ATXN2 intermediate-length CAG repeats with amyotrophic lateral sclerosis correlates with the distributions of normal CAG repeat alleles among individual ethnic populationsHiroya Naruse, Takashi Matsukawa, Hiroyuki Ishiura, et al.
Rinsho Shinkeigaku = Clinical Neurology|September 24, 2004
[A case of chronic inflammatory demyelinating polyneuropathy presenting with acute pain and SIADH followed by weakness of all four limbs 2 month after the first symptoms]Jun Mitsui, Izumi Sugimoto, Satoko Kano, et al.
Journal of Human Genetics|June 20, 2018
Novel mutations in the ALDH18A1 gene in complicated hereditary spastic paraplegia with cerebellar ataxia and cognitive impairmentKishin Koh, Hiroyuki Ishiura, Minako Beppu, et al.
Parkinsonism & Related Disorders|January 18, 2015
The first Japanese familial case of spinocerebellar ataxia 23 with a novel mutation in the PDYN geneKazumasa Saigoh, Jun Mitsui, Makito Hirano, et al.
The Laryngoscope|July 5, 2020
Esophageal Dysmotility is Common in Patients With Multiple System AtrophyRumi Ueha, Taku Sato, Takao Goto, et al.
Internal Medicine (Tokyo, Japan)|December 12, 2017
A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese PatientAkatsuki Kubota, Hiroyuki Ishiura, Jun Mitsui, et al.
Journal of the Peripheral Nervous System : JPNS|May 30, 2023
Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1Hiroya Naruse, So Okubo, Atsushi Sudo, et al.
Cerebellum (London, England)|November 30, 2021
Frequency of FMR1 Premutation Alleles in Patients with Undiagnosed Cerebellar Ataxia and Multiple System Atrophy in the Japanese PopulationAsem Almansour, Hiroyuki Ishiura, Jun Mitsui, et al.
Pageof 19