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Brain & Development|October 20, 2006
Disappearance of frontal N30 component of median nerve stimulated SSEPs in two young children with abnormal striatal lesionsYosuke Kato, Chisako Fukuda, Yoshihiro Maegaki, et al.
Glycobiology|May 5, 2009
Simultaneous quantification of glucosylceramide and galactosylceramide by normal-phase HPLC using O-phtalaldehyde derivatives prepared with sphingolipid ceramide N-deacylaseKota Zama, Yasuhiro Hayashi, Shinya Ito, et al.
Brain & Development|September 30, 2006
Acute encephalitis with refractory, repetitive partial seizures: case reports of this unusual post-encephalitic epilepsyYoshiaki Saito, Yoshihiro Maegaki, Riina Okamoto, et al.
Brain & Development|July 13, 2013
Nationwide survey of Arima syndrome: revised diagnostic criteria from epidemiological analysisMasayuki Itoh, Yuji Iwasaki, Kohsaku Ohno, et al.
Archives of Neurology|May 22, 2002
Contribution of the interleukin 4 gene to susceptibility to subacute sclerosing panencephalitisTakehiko Inoue, Ryutaro Kira, Futoshi Nakao, et al.
Biochimica Et Biophysica Acta|March 17, 2007
Enzyme enhancement activity of N-octyl-beta-valienamine on beta-glucosidase mutants associated with Gaucher diseaseKe Lei, Haruaki Ninomiya, Michitaka Suzuki, et al.
Steroids|October 4, 2005
Chemical synthesis of the 3-sulfooxy-7-N-acetylglucosaminyl-24-amidated conjugates of 3beta,7beta-dihydroxy-5-cholen-24-oic acid, and related compounds: unusual, major metabolites of bile acid in a patient with Niemann-Pick disease type C1Takashi Iida, Genta Kakiyama, Yohei Hibiya, et al.
Brain & Development|September 23, 2008
A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRITerumi Murakami, Yukiko K Hayashi, Megumu Ogawa, et al.
Biochimica Et Biophysica Acta|July 28, 2004
N-octyl-beta-valienamine up-regulates activity of F213I mutant beta-glucosidase in cultured cells: a potential chemical chaperone therapy for Gaucher diseaseHou Lin, Yuko Sugimoto, Yuki Ohsaki, et al.
Brain & Development|March 31, 2009
Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplicationsKeiko Shimojima, Takehiko Inoue, Ai Hoshino, et al.
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