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

Jun Tohyama

Showing results (41-50 of 102) with videos related to

Pageof 11
Sort By:
Epilepsia|June 26, 2009
Stiripentol open study in Japanese patients with Dravet syndromeYushi Inoue, Yoko Ohtsuka, Hirokazu Oguni, et al.
Brain & Development|October 17, 2016
Severe leukoencephalopathy with cortical involvement and peripheral neuropathy due to FOLR1 deficiencyYu Kobayashi, Jun Tohyama, Tomoyuki Akiyama, et al.
Epilepsia Open|April 21, 2022
Recurrence rates and risk factors for seizure recurrence following antiseizure medication withdrawal in adolescent patients with genetic generalized epilepsyTakao Komatsubara, Yu Kobayashi, Akiko Hiraiwa, et al.
Brain & Development|March 4, 2023
Efficacy of sirolimus for epileptic seizures in childhood associated with focal cortical dysplasia type IIHideaki Shiraishi, Tsuyoshi Teramoto, Saki Yokoshiki, et al.
American Journal of Human Genetics|August 2, 2007
A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome)Mitsuhiro Kato, Shinji Saitoh, Atsushi Kamei, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 12, 2013
Screening of male dialysis patients for fabry disease by plasma globotriaosylsphingosineHiroki Maruyama, Takuma Takata, Yutaka Tsubata, et al.
Medicine|July 22, 2016
Hypocretin-1 levels in the cerebrospinal fluid of patients with Percheron artery infarction with or without midbrain involvement: A case seriesKeisuke Suzuki, Tomoyuki Miyamoto, Masayuki Miyamoto, et al.
Journal of Human Genetics|September 24, 2025
Balanced chromosomal insertions as the mechanism of recurrent familial microstructural abnormalities: detailed analyses using long-read whole-genome sequencingHironao Shirai, Keiko Shimojima Yamamoto, Hirokazu Arai, et al.
The Kurume Medical Journal|June 17, 2021
A Single-Arm Open-Label Clinical Trial on the Efficacy and Safety of Sirolimus for Epileptic Seizures Associated with Focal Cortical Dysplasia Type II: A Study ProtocolAkiko Kada, Jun Tohyama, Hideaki Shiraishi, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Dandy-Walker malformation associated with heterozygous ZIC1 and ZIC4 deletion: Report of a new patientJun Tohyama, Mitsuhiro Kato, Sari Kawasaki, et al.
Pageof 11

Showing results (41-50 of 102) with videos related to

Sort By:
Pageof 11
Epilepsia|June 26, 2009
Stiripentol open study in Japanese patients with Dravet syndromeYushi Inoue, Yoko Ohtsuka, Hirokazu Oguni, et al.
Brain & Development|October 17, 2016
Severe leukoencephalopathy with cortical involvement and peripheral neuropathy due to FOLR1 deficiencyYu Kobayashi, Jun Tohyama, Tomoyuki Akiyama, et al.
Epilepsia Open|April 21, 2022
Recurrence rates and risk factors for seizure recurrence following antiseizure medication withdrawal in adolescent patients with genetic generalized epilepsyTakao Komatsubara, Yu Kobayashi, Akiko Hiraiwa, et al.
Brain & Development|March 4, 2023
Efficacy of sirolimus for epileptic seizures in childhood associated with focal cortical dysplasia type IIHideaki Shiraishi, Tsuyoshi Teramoto, Saki Yokoshiki, et al.
American Journal of Human Genetics|August 2, 2007
A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome)Mitsuhiro Kato, Shinji Saitoh, Atsushi Kamei, et al.
Clinical Journal of the American Society of Nephrology : CJASN|January 12, 2013
Screening of male dialysis patients for fabry disease by plasma globotriaosylsphingosineHiroki Maruyama, Takuma Takata, Yutaka Tsubata, et al.
Medicine|July 22, 2016
Hypocretin-1 levels in the cerebrospinal fluid of patients with Percheron artery infarction with or without midbrain involvement: A case seriesKeisuke Suzuki, Tomoyuki Miyamoto, Masayuki Miyamoto, et al.
Journal of Human Genetics|September 24, 2025
Balanced chromosomal insertions as the mechanism of recurrent familial microstructural abnormalities: detailed analyses using long-read whole-genome sequencingHironao Shirai, Keiko Shimojima Yamamoto, Hirokazu Arai, et al.
The Kurume Medical Journal|June 17, 2021
A Single-Arm Open-Label Clinical Trial on the Efficacy and Safety of Sirolimus for Epileptic Seizures Associated with Focal Cortical Dysplasia Type II: A Study ProtocolAkiko Kada, Jun Tohyama, Hideaki Shiraishi, et al.
American Journal of Medical Genetics. Part A|January 5, 2011
Dandy-Walker malformation associated with heterozygous ZIC1 and ZIC4 deletion: Report of a new patientJun Tohyama, Mitsuhiro Kato, Sari Kawasaki, et al.
Pageof 11