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Brain & Development
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July 20, 2021
Progressive cerebral atrophies in three children with COL4A1 mutations
Yuko Nakamura, Tohru Okanishi, Hiroyuki Yamada, et al.
Yonago Acta Medica
|
February 23, 2023
Phase Lag Analysis Scalp Electroencephalography May Predict Seizure Frequencies in Patients with Childhood Epilepsy with Centrotemporal Spikes
Masayoshi Oguri, Tetsuya Okazaki, Tohru Okanishi, et al.
Brain & Development
|
August 4, 2016
Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis
Tetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, et al.
Yonago Acta Medica
|
March 1, 2021
Clinical Characteristics of Fragile X Syndrome Patients in Japan
Tetsuya Okazaki, Kaori Adachi, Kaori Matsuura, et al.
DEN Open
|
May 12, 2025
Adequacy evaluation of 22-gauge needle endoscopic ultrasound-guided tissue acquisition samples and glass slides preparation for successful comprehensive genomic profiling testing: A single institute experience
Tami Nagatani, Yoji Wani, Masahiro Takatani, et al.
Brain & Development
|
September 18, 2012
Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study
Takashi Saito, Yoshiaki Saito, Kenji Sugai, et al.
Pediatric Neurology
|
January 19, 2016
Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata
Tetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, et al.
Molecules (Basel, Switzerland)
|
April 21, 2018
Probing the Inhibitor versus Chaperone Properties of sp²-Iminosugars towards Human β-Glucocerebrosidase: A Picomolar Chaperone for Gaucher Disease
Teresa Mena-Barragán, M Isabel García-Moreno, Alen Sevšek, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 12, 2021
FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
Hiroyuki Awano, Yoshihiko Saito, Mamiko Shimizu, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
July 7, 2022
Impaired neuronal integrity in traumatic brain injury detected by <sup>123</sup>I-iomazenil single photon emission computed tomography and MRI
Hiroki Kato, Jyoji Nakagawara, Kenji Hachisuka, et al.
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Search research articles
Search
Showing results (31-40 of 51) with videos related to
Sort By:
Page
of 6
Brain & Development
|
July 20, 2021
Progressive cerebral atrophies in three children with COL4A1 mutations
Yuko Nakamura, Tohru Okanishi, Hiroyuki Yamada, et al.
Yonago Acta Medica
|
February 23, 2023
Phase Lag Analysis Scalp Electroencephalography May Predict Seizure Frequencies in Patients with Childhood Epilepsy with Centrotemporal Spikes
Masayoshi Oguri, Tetsuya Okazaki, Tohru Okanishi, et al.
Brain & Development
|
August 4, 2016
Epileptic phenotype of FGFR3-related bilateral medial temporal lobe dysgenesis
Tetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, et al.
Yonago Acta Medica
|
March 1, 2021
Clinical Characteristics of Fragile X Syndrome Patients in Japan
Tetsuya Okazaki, Kaori Adachi, Kaori Matsuura, et al.
DEN Open
|
May 12, 2025
Adequacy evaluation of 22-gauge needle endoscopic ultrasound-guided tissue acquisition samples and glass slides preparation for successful comprehensive genomic profiling testing: A single institute experience
Tami Nagatani, Yoji Wani, Masahiro Takatani, et al.
Brain & Development
|
September 18, 2012
Late-onset epilepsy in children with acute febrile encephalopathy with prolonged convulsions: A clinical and encephalographic study
Takashi Saito, Yoshiaki Saito, Kenji Sugai, et al.
Pediatric Neurology
|
January 19, 2016
Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata
Tetsuya Okazaki, Yoshiaki Saito, Riyo Ueda, et al.
Molecules (Basel, Switzerland)
|
April 21, 2018
Probing the Inhibitor versus Chaperone Properties of sp²-Iminosugars towards Human β-Glucocerebrosidase: A Picomolar Chaperone for Gaucher Disease
Teresa Mena-Barragán, M Isabel García-Moreno, Alen Sevšek, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 12, 2021
FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients
Hiroyuki Awano, Yoshihiko Saito, Mamiko Shimizu, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
July 7, 2022
Impaired neuronal integrity in traumatic brain injury detected by <sup>123</sup>I-iomazenil single photon emission computed tomography and MRI
Hiroki Kato, Jyoji Nakagawara, Kenji Hachisuka, et al.
Page
of 6