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Journal of the Neurological Sciences|September 11, 2024
C9orf72 repeat expansions in Wakayama: One potential cause of amyotrophic lateral sclerosis in the Kii Peninsula, JapanSeiji Emori, Kodai Kume, Yoshiaki Nakayama, et al.
Neurology Research International|May 2, 2012
Transcranial magnetic stimulation with the maximum voluntary muscle contraction facilitates motor neuron excitability and muscle forceTetsuo Touge, Yoshiteru Urai, Kazuyo Ikeda, et al.
Rinsho Shinkeigaku = Clinical Neurology|May 31, 2013
[Successful treatment of HIV-associated chronic inflammatory demyelinating polyneuropathy by early initiation of highly active anti-retroviral therapy]Kodai Kume, Kazuyo Ikeda, Masaki Kamada, et al.
FEBS Letters|October 11, 2005
Inhibition of neuronal nitric-oxide synthase by phosphorylation at Threonine1296 in NG108-15 neuronal cellsTao Song, Naoya Hatano, Kodai Kume, et al.
Multiple Sclerosis and Related Disorders|January 4, 2019
Clinical significance of assaying anti-MOG antibody in cerebrospinal fluid in MOG-antibody-associated diseases: A case reportShingo Aoe, Kodai Kume, Tadayuki Takata, et al.
Internal Medicine (Tokyo, Japan)|July 10, 2018
Subacute Sensorimotor Neuropathy Accompanied by Anti-ganglioside GM1 Antibody in a Patient with Lung CancerNobuhiro Kanaji, Kodai Kume, Hitoshi Mizoguchi, et al.
Internal Medicine (Tokyo, Japan)|March 22, 2017
Acute Intermittent Porphyria Presenting with Posterior Reversible Encephalopathy Syndrome, Accompanied by Prolonged VasoconstrictionTadayuki Takata, Kodai Kume, Yohei Kokudo, et al.
Internal Medicine (Tokyo, Japan)|August 2, 2016
Dialysis-induced Subdural Hematoma in an Arachnoid Cyst Associated with Autosomal Dominant Polycystic Kidney DiseaseTadayuki Takata, Yohei Kokudo, Kodai Kume, et al.
Journal of Human Genetics|May 27, 2020
The first Japanese case of primary familial brain calcification caused by an MYORG variantKodai Kume, Tadayuki Takata, Hiroyuki Morino, et al.
Neuropathology and Applied Neurobiology|June 26, 2026
Neuropathological and Molecular Features Associated With a Heterozygous DNAJC7 Mutation in Amyotrophic Lateral SclerosisYoshiaki Nakayama, Kodai Kume, Takashi Baba, et al.
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