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Yohei Misumi

Showing results (41-50 of 138) with videos related to

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Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 11, 2022
Fibrinogen A α-chain amyloidosis associated with a rare frameshift pathogenic variant p.Arg547GlyfsTer21Masayoshi Tasaki, Toshiya Nomura, Koichi Uchiyama, et al.
Biochemistry and Biophysics Reports|December 28, 2020
Amyloid fibril formation is suppressed in microgravityHiroaki Matsushita, Aito Isoguchi, Masamitsu Okada, et al.
Annals of Rehabilitation Medicine|November 10, 2022
Effects of Intensive Exercise on Cognitive Dysfunction in Patients With Pure Cerebellar Degeneration: A Single-Arm Pilot StudyToshiya Shimamoto, Katsuhisa Uchino, Akira Mori, et al.
Muscle & Nerve|November 14, 2023
Correlation between a commercial electrophysiological test of sudomotor function and intraepidermal nerve fiber density in hereditary transthyretin amyloidosisTeruaki Masuda, Yohei Misumi, Toshiya Nomura, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2017
Long-term effects of liver transplantation on small-fiber dysfunction in Japanese transthyretin (ATTR) V30M hereditary amyloidosis with polyneuropathy (FAP)Konen Obayashi, Mitsuharu Ueda, Taro Yamashita, et al.
Orphanet Journal of Rare Diseases|September 2, 2025
Genetic and clinical features of hereditary transthyretin amyloidosis: a decade of experience at a Japanese referral centerToshiya Nomura, Yohei Misumi, Masayoshi Tasaki, et al.
Clinical Case Reports|September 11, 2023
Heterozygous c.175C>T variant in <i>PURA</i> gene causes severe developmental delayYusuke Noda, Jun Kido, Yohei Misumi, et al.
Human Pathology|July 23, 2011
Relationship between amyloid deposition and intracellular structural changes in familial amyloidotic polyneuropathyYohei Misumi, Mitsuharu Ueda, Konen Obayashi, et al.
Human Genome Variation|March 14, 2026
Non-pterygium Escobar syndrome from compound-heterozygous CHRNG variants: genotype-phenotype insightsJun Kido, Hiroe Ueno, Yohei Misumi, et al.
Neurology|November 7, 2018
Teaching NeuroImages: Morphology of lumbosacral dorsal root ganglia and plexus in hereditary transthyretin amyloidosisTeruaki Masuda, Mitsuharu Ueda, Mika Kitajima, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 11, 2022
Fibrinogen A α-chain amyloidosis associated with a rare frameshift pathogenic variant p.Arg547GlyfsTer21Masayoshi Tasaki, Toshiya Nomura, Koichi Uchiyama, et al.
Biochemistry and Biophysics Reports|December 28, 2020
Amyloid fibril formation is suppressed in microgravityHiroaki Matsushita, Aito Isoguchi, Masamitsu Okada, et al.
Annals of Rehabilitation Medicine|November 10, 2022
Effects of Intensive Exercise on Cognitive Dysfunction in Patients With Pure Cerebellar Degeneration: A Single-Arm Pilot StudyToshiya Shimamoto, Katsuhisa Uchino, Akira Mori, et al.
Muscle & Nerve|November 14, 2023
Correlation between a commercial electrophysiological test of sudomotor function and intraepidermal nerve fiber density in hereditary transthyretin amyloidosisTeruaki Masuda, Yohei Misumi, Toshiya Nomura, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 25, 2017
Long-term effects of liver transplantation on small-fiber dysfunction in Japanese transthyretin (ATTR) V30M hereditary amyloidosis with polyneuropathy (FAP)Konen Obayashi, Mitsuharu Ueda, Taro Yamashita, et al.
Orphanet Journal of Rare Diseases|September 2, 2025
Genetic and clinical features of hereditary transthyretin amyloidosis: a decade of experience at a Japanese referral centerToshiya Nomura, Yohei Misumi, Masayoshi Tasaki, et al.
Clinical Case Reports|September 11, 2023
Heterozygous c.175C>T variant in <i>PURA</i> gene causes severe developmental delayYusuke Noda, Jun Kido, Yohei Misumi, et al.
Human Pathology|July 23, 2011
Relationship between amyloid deposition and intracellular structural changes in familial amyloidotic polyneuropathyYohei Misumi, Mitsuharu Ueda, Konen Obayashi, et al.
Human Genome Variation|March 14, 2026
Non-pterygium Escobar syndrome from compound-heterozygous CHRNG variants: genotype-phenotype insightsJun Kido, Hiroe Ueno, Yohei Misumi, et al.
Neurology|November 7, 2018
Teaching NeuroImages: Morphology of lumbosacral dorsal root ganglia and plexus in hereditary transthyretin amyloidosisTeruaki Masuda, Mitsuharu Ueda, Mika Kitajima, et al.
Pageof 14