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American Journal of Medical Genetics. Part A|May 8, 2014
Refinement of the deletion in 8q22.2-q22.3: the minimum deletion size at 8q22.3 related to intellectual disability and epilepsyYukiko Kuroda, Ikuko Ohashi, Toshiyuki Saito, et al.Brain & Development|February 15, 2011
Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemiaYu Tsuyusaki, Hiroko Shimbo, Takahito Wada, et al.Brain & Development|May 14, 2014
Effect of CYP2C19 polymorphisms on stiripentol administration in Japanese cases of Dravet syndromeTakeshi Kouga, Hiroko Shimbo, Mizue Iai, et al.Brain & Development|September 21, 2010
5,10-Methylenetetrahydrofolate reductase deficiency with progressive polyneuropathy in an infantMegumi Tsuji, Atsushi Takagi, Kiyoko Sameshima, et al.No to Hattatsu = Brain and Development|February 23, 2012
[Clinical characteristics of acute encephalopathies associated with influenza H1N1-2009 in children]Yoshihiro Watanabe, Megumi Tsuji, Kiyoko Sameshima, et al.Brain & Development|December 5, 2020
Infection-associated decrease of serum creatine kinase levels in Fukuyama congenital muscular dystrophySaoko Takeshita, Yoshiaki Saito, Yoshitaka Oyama, et al.The Journal of Pediatrics|January 30, 2002
Peroxisomal acyl CoA oxidase deficiencyYasuyuki Suzuki, Mizue Iai, Atsushi Kamei, et al.Epilepsy Research|February 20, 2022
Elevation of brain gamma-aminobutyric acid levels is associated with vigabatrin-associated brain abnormalities on magnetic resonance imagingAzusa Ikeda, Moyoko Tomiyasu, Ayako Yamamoto, et al.Brain & Development|April 3, 2025
Clinical characteristics and radiological features of tubulinopathy: A single-center retrospective study in JapanTamaki Ikegawa, Kana Osada, Azusa Ikeda, et al.Journal of Human Genetics|December 5, 2014
Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathyHirofumi Kodera, Hitoshi Osaka, Mizue Iai, et al.Pageof 4