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Frontiers in Neurology|July 31, 2024
Genotype-relevant neuroimaging features in low-grade epilepsy-associated tumorsKeiya Iijima, Hiroyuki Fujii, Fumio Suzuki, et al.
Brain & Development|May 19, 2022
Long-term changes in electroencephalogram findings in a girl with a nonsense SMC1A variant: A case reportKazuhiko Hashimoto, Shimpei Baba, Eiji Nakagawa, et al.
Internal Medicine (Tokyo, Japan)|August 26, 2021
Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear InclusionsTomoya Kawazoe, Shinsuke Tobisawa, Keizo Sugaya, et al.
Human Molecular Genetics|July 14, 2011
Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagySatomi Mitsuhashi, Hideyuki Hatakeyama, Minako Karahashi, et al.
Pediatric Neurology|November 14, 2020
Hyperglycemic Crisis in Patients With Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS)Taira Toki, Yuko Shimizu-Motohashi, Hirofumi Komaki, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 12, 2025
Substitutions of nucleotides at the 3' ends of COL6A1/2/3 exons induce exon skipping associated with collagen VI-related muscular dystrophies and therapeutic strategiesSeung-Ah Lee, Megumu Ogawa, Yoshihiko Saito, et al.
Journal of Neuropathology and Experimental Neurology|July 19, 2012
Delayed maturation and differentiation of neurons in focal cortical dysplasia with the transmantle sign: analysis of layer-specific marker expressionTakafumi Sakakibara, Sayuri Sukigara, Takashi Saito, et al.
Scientific Reports|June 18, 2015
Increased cerebrospinal fluid fibrinogen in major depressive disorderKotaro Hattori, Miho Ota, Daimei Sasayama, et al.
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