Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Shinsuke Tobisawa

Showing results (1-10 of 33) with videos related to

Pageof 4
Sort By:
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 6, 2017
Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-proteinYuki Sakamoto, Toshio Shimizu, Shinsuke Tobisawa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 13, 2017
Prevalence and clinical characteristics of corticobasal syndrome with an initial symptom outside of the upper limbYuki Sakamoto, Toshio Shimizu, Shinsuke Tobisawa, et al.
Journal of Neurology|November 3, 2010
Deterioration of MRI findings related to Jarisch-Herxheimer reaction in a patient with neurosyphilisJunpei Kobayashi, Yasuko Nakagawa, Shinsuke Tobisawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 22, 2021
Tufted astrocyte-like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?Taku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Internal Medicine (Tokyo, Japan)|January 18, 2006
A variant form of nasogastric tube syndromeEiji Isozaki, Shinsuke Tobisawa, Rie Naito, et al.
Journal of the Neurological Sciences|July 12, 2020
Cerebral white matter tau-positive granular glial pathology as a characteristic pathological feature in long survivors of multiple system atrophyTaku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Journal of Neuropathology and Experimental Neurology|February 25, 2023
Differential immunophenotypes of neuronal cytoplasmic inclusions in the dentate gyrus of multiple system atrophy and their association with clinicopathological featuresTaku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Clinical Neurology and Neurosurgery|June 24, 2020
Clinical characteristics of children and adults with anti-N-methyl-D-aspartate receptor encephalitisRyohei Norioka, Satoko Kumada, Shinsuke Tobisawa, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 26, 2012
[Eye movement disturbance in multiple system atrophy: chronological study of 50 patients]Eiji Isozaki, Shinsuke Tobisawa, Rie Naito, et al.
Clinical Neurology and Neurosurgery|April 21, 2023
Dopa-responsive dystonia in spinocerebellar ataxia 6: A case reportJun Ikezawa, Rui Shimazaki, Shinsuke Tobisawa, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 6, 2017
Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-proteinYuki Sakamoto, Toshio Shimizu, Shinsuke Tobisawa, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 13, 2017
Prevalence and clinical characteristics of corticobasal syndrome with an initial symptom outside of the upper limbYuki Sakamoto, Toshio Shimizu, Shinsuke Tobisawa, et al.
Journal of Neurology|November 3, 2010
Deterioration of MRI findings related to Jarisch-Herxheimer reaction in a patient with neurosyphilisJunpei Kobayashi, Yasuko Nakagawa, Shinsuke Tobisawa, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|December 22, 2021
Tufted astrocyte-like glia in two autopsy cases of multiple system atrophy: Is it a concomitant neurodegenerative disorder with multiple system atrophy and progressive supranuclear palsy?Taku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Internal Medicine (Tokyo, Japan)|January 18, 2006
A variant form of nasogastric tube syndromeEiji Isozaki, Shinsuke Tobisawa, Rie Naito, et al.
Journal of the Neurological Sciences|July 12, 2020
Cerebral white matter tau-positive granular glial pathology as a characteristic pathological feature in long survivors of multiple system atrophyTaku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Journal of Neuropathology and Experimental Neurology|February 25, 2023
Differential immunophenotypes of neuronal cytoplasmic inclusions in the dentate gyrus of multiple system atrophy and their association with clinicopathological featuresTaku Homma, Yoko Mochizuki, Shinsuke Tobisawa, et al.
Clinical Neurology and Neurosurgery|June 24, 2020
Clinical characteristics of children and adults with anti-N-methyl-D-aspartate receptor encephalitisRyohei Norioka, Satoko Kumada, Shinsuke Tobisawa, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 26, 2012
[Eye movement disturbance in multiple system atrophy: chronological study of 50 patients]Eiji Isozaki, Shinsuke Tobisawa, Rie Naito, et al.
Clinical Neurology and Neurosurgery|April 21, 2023
Dopa-responsive dystonia in spinocerebellar ataxia 6: A case reportJun Ikezawa, Rui Shimazaki, Shinsuke Tobisawa, et al.
Pageof 4