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BMC Neurology|November 10, 2021
A p.Arg499His mutation in SPAST is associated with infantile-onset complicated spastic paraplegia: a case report and review of the literatureHaitian Nan, Hiroshi Shiraku, Tomoko Mizuno, et al.
Annals of the New York Academy of Sciences|November 16, 2004
Nefiracetam attenuates methamphetamine-induced discriminative stimulus effects in ratsYijin Yan, Tomoko Mizuno, Atsumi Nitta, et al.
The Journal of Obstetrics and Gynaecology Research|May 29, 2015
Novel pathophysiological cause for post-partum hemorrhage: Case report of post-partum hemorrhage with occult abnormal artery diagnosed on pelvic angiographyShigenori Iwagaki, Tatsuhiko Miyazaki, Tomoko Mizuno, et al.
Neuropsychobiology|January 7, 2012
Serotonin transporter gene promoter polymorphism and alexithymiaMichiko Kano, Tomoko Mizuno, Yuko Kawano, et al.
Behavioural Brain Research|July 22, 2006
Discriminative-stimulus effects of methamphetamine and morphine in rats are attenuated by cAMP-related compoundsYijin Yan, Atsumi Nitta, Tomoko Mizuno, et al.
Mutation Research|May 15, 2007
Quantification of a potent mutagenic 4-amino-3,3'-dichloro-5,4'-dinitrobiphenyl (ADDB) and the related chemicals in water from the Waka River in Wakayama, JapanTomoko Mizuno, Takeji Takamura-Enya, Tetsushi Watanabe, et al.
Molecular Pharmacology|April 23, 2004
Regulations of methamphetamine reward by extracellular signal-regulated kinase 1/2/ets-like gene-1 signaling pathway via the activation of dopamine receptorsHiroyuki Mizoguchi, Kiyofumi Yamada, Makoto Mizuno, et al.
Brain & Development|November 27, 2020
Clinical variations of epileptic syndrome associated with PACS2 variantTomoko Mizuno, Rie Miyata, Akira Hojo, et al.
BMC Neurology|November 1, 2023
Changes in electrophysiological findings of spinal muscular atrophy type I after the administration of nusinersen and onasemnogene abeparvovec: two case reportsTomoko Mizuno, Tadashi Kanouchi, Yumie Tamura, et al.
Brain & Development|March 23, 2019
Infantile-onset spinocerebellar ataxia type 5 associated with a novel SPTBN2 mutation: A case reportTomoko Mizuno, Ayako Kashimada, Toshihiro Nomura, et al.
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