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

Satoko Kumada

Showing results (31-40 of 74) with videos related to

Pageof 8
Sort By:
European Journal of Medical Genetics|September 3, 2020
A severe case of status dystonicus caused by a de novo KMT2B missense mutationSadao Nakamura, Yasutsugu Chinen, Kazuhito Satou, et al.
Brain & Development|February 18, 2020
A questionnaire survey on the efficacy of various treatments for dyskinetic cerebral palsy due to preterm bilirubin encephalopathyYukihiro Kitai, Satori Hirai, Naomi Okuyama, et al.
Epilepsy & Behavior Reports|August 29, 2024
Abnormal theta-band rhythm: EEG abnormality as potential biomarkers for disease severity in pediatric anti-NMDAR encephalitisYumie Tamura, Mitsumasa Fukuda, Akihiko Ishiyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 17, 2024
[Initiatives for supporting the health care transition in various regions: activities of transitional care support centers]Yoko Mochizuki, Katsuhisa Ogata, Satoko Kumada, et al.
Neonatology|March 21, 2021
Neonatal Jaundice in Preterm Infants with Bilirubin EncephalopathyAkihisa Okumura, Shintaro Ichimura, Masahiro Hayakawa, et al.
Brain & Development|August 15, 2009
The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusionNaoyuki Tanuma, Rie Miyata, Satoko Kumada, et al.
Brain & Development|May 7, 2005
Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survivalYasuo Hachiya, Hidee Arai, Masaharu Hayashi, et al.
Molecular Genetics and Metabolism Reports|January 21, 2025
Efficacy and safety of avalglucosidase alfa in Japanese patients with late-onset and infantile-onset Pompe diseases: A case series from clinical trialsMadoka Mori-Yoshimura, Hirotaka Ohki, Hideaki Mashimo, et al.
Brain & Development|April 22, 2018
Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 geneYohane Miyata, Ken Saida, Satoko Kumada, et al.
Frontiers in Neurology|June 16, 2018
Resting-State Pallidal-Cortical Oscillatory Couplings in Patients With Predominant Phasic and Tonic DystoniaFusako Yokochi, Kenji Kato, Hirokazu Iwamuro, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
European Journal of Medical Genetics|September 3, 2020
A severe case of status dystonicus caused by a de novo KMT2B missense mutationSadao Nakamura, Yasutsugu Chinen, Kazuhito Satou, et al.
Brain & Development|February 18, 2020
A questionnaire survey on the efficacy of various treatments for dyskinetic cerebral palsy due to preterm bilirubin encephalopathyYukihiro Kitai, Satori Hirai, Naomi Okuyama, et al.
Epilepsy & Behavior Reports|August 29, 2024
Abnormal theta-band rhythm: EEG abnormality as potential biomarkers for disease severity in pediatric anti-NMDAR encephalitisYumie Tamura, Mitsumasa Fukuda, Akihiko Ishiyama, et al.
Rinsho Shinkeigaku = Clinical Neurology|November 17, 2024
[Initiatives for supporting the health care transition in various regions: activities of transitional care support centers]Yoko Mochizuki, Katsuhisa Ogata, Satoko Kumada, et al.
Neonatology|March 21, 2021
Neonatal Jaundice in Preterm Infants with Bilirubin EncephalopathyAkihisa Okumura, Shintaro Ichimura, Masahiro Hayakawa, et al.
Brain & Development|August 15, 2009
The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusionNaoyuki Tanuma, Rie Miyata, Satoko Kumada, et al.
Brain & Development|May 7, 2005
Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survivalYasuo Hachiya, Hidee Arai, Masaharu Hayashi, et al.
Molecular Genetics and Metabolism Reports|January 21, 2025
Efficacy and safety of avalglucosidase alfa in Japanese patients with late-onset and infantile-onset Pompe diseases: A case series from clinical trialsMadoka Mori-Yoshimura, Hirotaka Ohki, Hideaki Mashimo, et al.
Brain & Development|April 22, 2018
Periventricular small cystic lesions in a patient with Coffin-Lowry syndrome who exhibited a novel mutation in the RPS6KA3 geneYohane Miyata, Ken Saida, Satoko Kumada, et al.
Frontiers in Neurology|June 16, 2018
Resting-State Pallidal-Cortical Oscillatory Couplings in Patients With Predominant Phasic and Tonic DystoniaFusako Yokochi, Kenji Kato, Hirokazu Iwamuro, et al.
Pageof 8