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Brain & Development|February 20, 2007
Transient splenial lesions in children with "benign convulsions with gastroenteritis"Jun Natsume, Misako Naiki, Taro Yokotsuka, et al.
Brain & Development|September 11, 2007
Effect of corticosteroids in a twin child with idiopathic localization-related epilepsyAyako Sofue, Misako Naiki, Taro Yokotsuka, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
MBTPS2 mutation causes BRESEK/BRESHECK syndromeMisako Naiki, Seiji Mizuno, Kenichiro Yamada, et al.
American Journal of Medical Genetics. Part A|January 31, 2014
Clinical characterization and identification of duplication breakpoints in a Japanese family with Xq28 duplication syndrome including MECP2Daisuke Fukushi, Kenichiro Yamada, Noriko Nomura, et al.
Nucleosides, Nucleotides & Nucleic Acids|December 3, 2011
Molecular analysis of X-linked inborn errors of purine metabolism: HPRT1 and PRPS1 mutationsYasukazu Yamada, Kenichiro Yamada, Noriko Nomura, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Mutations in HADHB, which encodes the β-subunit of mitochondrial trifunctional protein, cause infantile onset hypoparathyroidism and peripheral polyneuropathyMisako Naiki, Nobuhiko Ochi, Yusuke S Kato, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosisKenichiro Yamada, Misako Naiki, Shin Hoshino, et al.
Epilepsia|June 6, 2019
Hippocampal diffusion abnormality after febrile status epilepticus is related to subsequent epilepsySetsuri Yokoi, Hiroyuki Kidokoro, Hiroyuki Yamamoto, et al.
Epilepsia|November 19, 2011
Acute encephalopathy in children with Dravet syndromeAkihisa Okumura, Mitsugu Uematsu, George Imataka, et al.
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