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Journal of Neural Transmission (Vienna, Austria : 1996)|November 10, 2016
Vasomotor regulation in patients with multiple system atrophyKazumasa Shindo, Mai Tsuchiya, Yuta Ichinose, 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.
Molecular Genetics & Genomic Medicine|December 27, 2019
VPS13D-related disorders presenting as a pure and complicated form of hereditary spastic paraplegiaKishin Koh, Hiroyuki Ishiura, Haruo Shimazaki, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 22, 2020
Sympathetic outflow to skin predicts central autonomic dysfunction in multiple system atrophyKazumasa Shindo, Toko Fukao, Naofumi Kurita, et al.
Journal of Human Genetics|October 11, 2018
PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegiaKishin Koh, Yuta Ichinose, Hiroyuki Ishiura, et al.
Journal of Human Genetics|November 10, 2018
Correction: PLA2G6-associated neurodegeneration presenting as a complicated form of hereditary spastic paraplegiaKishin Koh, Yuta Ichinose, Hiroyuki Ishiura, et al.
Journal of the Neurological Sciences|August 20, 2015
No relation between sympathetic outflow to muscles and respiratory function in amyotrophic lateral sclerosisKazumasa Shindo, Mai Tsuchiya, Yuta Ichinose, et al.
Journal of Human Genetics|July 23, 2020
RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxiaMai Tsuchiya, Haitian Nan, Kishin Koh, et al.
Clinical Neurology and Neurosurgery|March 12, 2016
Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8Yuta Ichinose, Kishin Koh, Megumi Fukumoto, et al.
Journal of Clinical Hypertension (Greenwich, Conn.)|November 17, 2020
Age-related changes in blood pressure and heart rates of patients with Parkinson's diseaseKazumasa Shindo, Yuto Morishima, Yumi Suwa, et al.
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