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Rinsho Shinkeigaku = Clinical Neurology|October 9, 2004
[A case of middle-aged onset sialidosis type I]Yuka Sakazume, Makoto Tanaka, Itsuo Isobe, et al.Brain & Development|April 26, 2025
Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide surveyTetsuya Okazaki, Chisako Aoki, Kaori Adachi, et al.Annals of Neurology|September 3, 2002
Niemann-Pick type C disease: accelerated neurofibrillary tangle formation and amyloid beta deposition associated with apolipoprotein E epsilon 4 homozygosityYuko Saito, Kinuko Suzuki, Eiji Nanba, et al.Brain & Development|June 12, 2012
The chaperone activity and toxicity of ambroxol on Gaucher cells and normal miceZhuo Luan, Linjing Li, Katsumi Higaki, et al.Brain & Development|May 30, 2006
Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouseMasumi Inagaki, Kaori Kon, Seiko Suzuki, et al.Experimental Cell Research|December 9, 2020
Establishment of FXS-A9 panel with a single human X chromosome from fragile X syndrome-associated individualYuji Nakayama, Kaori Adachi, Nofirifumi Shioda, et al.Brain & Development|April 9, 2008
A case of galactosialidosis with a homozygous Q49R point mutationNaoko Matsumoto, Kenjiro Gondo, Johji Kukita, et al.Human Mutation|March 17, 2004
Novel TSC2 mutations and decreased expression of tuberin in cultured tumor cells with an insertion mutationJian-Hua Feng, Toshiyuki Yamamoto, Eiji Nanba, et al.Brain & Development|March 17, 2007
Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndromeNoriko Itaba-Matsumoto, Shinji Maegawa, Hidehisa Yamagata, et al.Proceedings of the Japan Academy. Series B, Physical and Biological Sciences|April 16, 2009
Aberrant promoter methylation and expression of the imprinted PEG3 gene in gliomaSusumu Otsuka, Shinji Maegawa, Ayumi Takamura, et al.Pageof 15