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Clinical Case Reports|January 24, 2015
A case of Barber-Say syndrome in a male Japanese newbornKenichi Suga, Miki Shono, Aya Goji, et al.
Brain & Development|March 25, 2023
A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocationTatsuo Mori, Masamune Sakamoto, Takahiro Tayama, et al.
Brain & Development|March 13, 2024
A female case of L1 syndrome that may have developed due to skewed X inactivationTatsuo Mori, Mutsuki Nakano, Takahiro Tayama, et al.
The Journal of Medical Investigation : JMI|May 12, 2024
Bilateral Prefrontal Cortex Blood Flow Dynamics during Silent and Oral Reading Using Near-Infrared SpectroscopyNatsue Nozaki, Kenji Mori, Tetsuya Tanioka, et al.
Human Genome Variation|September 23, 2016
A novel missense mutation of COL5A2 in a patient with Ehlers-Danlos syndromeMiki Watanabe, Ryuji Nakagawa, Takuya Naruto, et al.
The Journal of Medical Investigation : JMI|October 27, 2024
Hemodynamics of the left cerebral hemisphere during silent reading:analysis using near-infrared spectroscopyRuriko Yamashita, Kumi Takahashi, Keiko Mori, et al.
Human Genome Variation|November 22, 2016
Exome-first approach identified a novel gloss deletion associated with Lowe syndromeMiki Watanabe, Ryuji Nakagawa, Tomohiro Kohmoto, et al.
The Journal of Medical Investigation : JMI|March 31, 2015
Neuroimaging in autism spectrum disorders: 1H-MRS and NIRS studyKenji Mori, Yoshihiro Toda, Hiromichi Ito, et al.
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