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European Journal of Medical Genetics
|
September 3, 2020
A severe case of status dystonicus caused by a de novo KMT2B missense mutation
Sadao 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 encephalopathy
Yukihiro 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 encephalitis
Yumie 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 Encephalopathy
Akihisa 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 diffusion
Naoyuki Tanuma, Rie Miyata, Satoko Kumada, et al.
Brain & Development
|
May 7, 2005
Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survival
Yasuo 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 trials
Madoka 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 gene
Yohane 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 Dystonia
Fusako Yokochi, Kenji Kato, Hirokazu Iwamuro, et al.
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of 8
Search research articles
Search
Showing results (31-40 of 74) with videos related to
Sort By:
Page
of 8
European Journal of Medical Genetics
|
September 3, 2020
A severe case of status dystonicus caused by a de novo KMT2B missense mutation
Sadao 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 encephalopathy
Yukihiro 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 encephalitis
Yumie 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 Encephalopathy
Akihisa 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 diffusion
Naoyuki Tanuma, Rie Miyata, Satoko Kumada, et al.
Brain & Development
|
May 7, 2005
Autonomic dysfunction in cases of spinal muscular atrophy type 1 with long survival
Yasuo 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 trials
Madoka 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 gene
Yohane 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 Dystonia
Fusako Yokochi, Kenji Kato, Hirokazu Iwamuro, et al.
Page
of 8