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Hiroyuki Morino

Showing results (1-10 of 88) with videos related to

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Brain and Nerve = Shinkei Kenkyu No Shinpo|September 27, 2016
[Causative Genes for Amyotrophic Lateral Sclerosis]Hirofumi Maruyama, Hiroyuki Morino, Hideshi Kawakami
Hiroshima Journal of Medical Sciences|November 8, 2011
Detection of large expansions in SCA8 using a fluorescent repeat-primed PCR assayEiji Tanaka, Hirofumi Maruyama, Hiroyuki Morino, et al.
Internal and Emergency Medicine|December 12, 2022
Extubation failure due to atypical parkinsonism with negligible motor and variable non-motor symptoms associated with a variant of DCTN1Hidetada Yamada, Shuichiro Neshige, Hiroyuki Morino, et al.
Internal Medicine (Tokyo, Japan)|December 2, 2008
Cytotoxic edema in neuro-Behcet's disease ?Isha Shrestha, Tomohiko Ohshita, Hiromitsu Naka, et al.
American Journal of Neurodegenerative Disease|March 22, 2013
Convenient diagnosis of spinal and bulbar muscular atrophy using a microchip electrophoresis systemHirofumi Maruyama, Hiroyuki Morino, Yuishin Izumi, et al.
BMC Neurology|January 9, 2014
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patientHiroyuki Morino, Ryosuke Miyamoto, Shizuo Ohnishi, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|June 21, 2002
[A case of late onset mitochondrial neuromyopathy]Kie Honjo, Yasuyo Mimori, Hiroyuki Morino, et al.
Neurobiology of Aging|May 10, 2011
Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian populationKatsunobu Sugihara, Hirofumi Maruyama, Masaki Kamada, et al.
Journal of the Neurological Sciences|October 5, 2007
The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxiaEiji Tanaka, Hirofumi Maruyama, Hiroyuki Morino, et al.
Journal of Medical Case Reports|December 14, 2011
Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case seriesHiroki Ueno, Keitaro Kobatake, Masayasu Matsumoto, et al.
Pageof 9

Showing results (1-10 of 88) with videos related to

Sort By:
Pageof 9
Brain and Nerve = Shinkei Kenkyu No Shinpo|September 27, 2016
[Causative Genes for Amyotrophic Lateral Sclerosis]Hirofumi Maruyama, Hiroyuki Morino, Hideshi Kawakami
Hiroshima Journal of Medical Sciences|November 8, 2011
Detection of large expansions in SCA8 using a fluorescent repeat-primed PCR assayEiji Tanaka, Hirofumi Maruyama, Hiroyuki Morino, et al.
Internal and Emergency Medicine|December 12, 2022
Extubation failure due to atypical parkinsonism with negligible motor and variable non-motor symptoms associated with a variant of DCTN1Hidetada Yamada, Shuichiro Neshige, Hiroyuki Morino, et al.
Internal Medicine (Tokyo, Japan)|December 2, 2008
Cytotoxic edema in neuro-Behcet's disease ?Isha Shrestha, Tomohiko Ohshita, Hiromitsu Naka, et al.
American Journal of Neurodegenerative Disease|March 22, 2013
Convenient diagnosis of spinal and bulbar muscular atrophy using a microchip electrophoresis systemHirofumi Maruyama, Hiroyuki Morino, Yuishin Izumi, et al.
BMC Neurology|January 9, 2014
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patientHiroyuki Morino, Ryosuke Miyamoto, Shizuo Ohnishi, et al.
Nihon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics|June 21, 2002
[A case of late onset mitochondrial neuromyopathy]Kie Honjo, Yasuyo Mimori, Hiroyuki Morino, et al.
Neurobiology of Aging|May 10, 2011
Screening for OPTN mutations in amyotrophic lateral sclerosis in a mainly Caucasian populationKatsunobu Sugihara, Hirofumi Maruyama, Masaki Kamada, et al.
Journal of the Neurological Sciences|October 5, 2007
The CNTN4 c.4256C>T mutation is rare in Japanese with inherited spinocerebellar ataxiaEiji Tanaka, Hirofumi Maruyama, Hiroyuki Morino, et al.
Journal of Medical Case Reports|December 14, 2011
Severe brain atrophy after long-term survival seen in siblings with familial amyotrophic lateral sclerosis and a mutation in the optineurin gene: a case seriesHiroki Ueno, Keitaro Kobatake, Masayasu Matsumoto, et al.
Pageof 9