| Nitric oxide-mediated modulation of calcium/calmodulin-dependent protein kinase II T Song, N Hatano, T Kambe, Y Miyamoto, H Ihara, H Yamamoto, ... Biochemical Journal 412 (2), 223-231, 2008 | 56 | 2008 |
| Significance of the hot-cross bun sign on T2*-weighted MRI for the diagnosis of multiple system atrophy K Deguchi, K Ikeda, K Kume, T Takata, Y Kokudo, M Kamada, T Touge, ... Journal of neurology 262, 1433-1439, 2015 | 45 | 2015 |
| Serum microRNA expression profiling in patients with multiple system atrophy K Kume, H Iwama, K Deguchi, K Ikeda, T Takata, Y Kokudo, M Kamada, ... Molecular Medicine Reports 17 (1), 852-860, 2018 | 35 | 2018 |
| Three cases of non-carryover fingolimod-PML: Is the risk in Japan increased? J Nakahara, L Tomaske, K Kume, T Takata, M Kamada, K Deguchi, ... Neurology: Neuroimmunology & Neuroinflammation 6 (3), e559, 2019 | 33 | 2019 |
| Neuromyelitis optica spectrum disorder presenting with repeated hypersomnia due to involvement of the hypothalamus and hypothalamus-amygdala linkage K Kume, K Deguchi, K Ikeda, T Takata, Y Kokudo, M Kamada, T Touge, ... Multiple Sclerosis Journal 21 (7), 960-962, 2015 | 27 | 2015 |
| p90 RSK-1 associates with and inhibits neuronal nitric oxide synthase T Song, K Sugimoto, H Ihara, A Mizutani, N Hatano, K Kume, T Kambe, ... Biochemical Journal 401 (2), 391-398, 2007 | 27 | 2007 |
| FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report M Toko, T Ohshita, T Kurashige, H Morino, K Kume, H Yamashita, ... BMC neurology 21, 1-5, 2021 | 25 | 2021 |
| Inhibition of neuronal nitric-oxide synthase by phosphorylation at Threonine1296 in NG108-15 neuronal cells T Song, N Hatano, K Kume, K Sugimoto, F Yamaguchi, M Tokuda, ... FEBS letters 579 (25), 5658-5662, 2005 | 25 | 2005 |
| Acute intermittent porphyria presenting with posterior reversible encephalopathy syndrome, accompanied by prolonged vasoconstriction T Takata, K Kume, Y Kokudo, K Ikeda, M Kamada, T Touge, K Deguchi, ... Internal Medicine 56 (6), 713-717, 2017 | 24 | 2017 |
| Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report K Kume, H Morino, R Miyamoto, Y Matsuda, R Ohsawa, Y Kanaya, ... BMC Medical Genetics 21, 1-4, 2020 | 13 | 2020 |
| Aggressive periodontitis and NOD2 variants N Mizuno, K Kume, Y Nagatani, S Matsuda, T Iwata, K Ouhara, M Kajiya, ... Journal of Human Genetics 65 (10), 841-846, 2020 | 13 | 2020 |
| Co-morbidity of progressive supranuclear palsy and amyotrophic lateral sclerosis: a clinical-pathological case report K Fujita, T Matsubara, R Miyamoto, H Sumikura, T Takeuchi, ... BMC neurology 19, 1-8, 2019 | 13 | 2019 |
| Optineurin regulates osteoblastogenesis through STAT1 N Mizuno, T Iwata, R Ohsawa, K Ouhara, S Matsuda, M Kajiya, Y Matsuda, ... Biochemical and Biophysical Research Communications 525 (4), 889-894, 2020 | 11 | 2020 |
| Clinical significance of assaying anti-MOG antibody in cerebrospinal fluid in MOG-antibody-associated diseases: a case report S Aoe, K Kume, T Takata, T Touge, K Kaneko, I Nakashima, K Deguchi, ... Multiple sclerosis and related disorders 28, 165-166, 2019 | 11 | 2019 |
| Unilateral mydriatic tonic pupil as an early isolated symptom of neurosyphilis T Takata, M Kamada, K Ikeda, K Kume, Y Kokudo, T Touge, K Deguchi, ... Journal of the Neurological Sciences 344 (1), 219-220, 2014 | 11 | 2014 |
| Usefulness of the modified F-ratio for assessmentsof proximal conduction in chronic inflammatory demyelinating polyneuropathy superimposed onCharcot Marie–Tooth disease type 1A K Kume, K Deguchi, K Ikeda, T Takata, Y Kokudo, M Kamada, ... Journal of the Neurological Sciences 1 (343), 237-239, 2014 | 10 | 2014 |
| Biallelic mutation of HSD17B4 induces middle age–onset spinocerebellar ataxia Y Matsuda, H Morino, R Miyamoto, T Kurashige, K Kume, N Mizuno, ... Neurology: Genetics 6 (1), e396, 2020 | 9 | 2020 |
| Successful treatment of HIV-associated chronic inflammatory demyelinating polyneuropathy by early initiation of highly active anti-retroviral therapy K Kume, K Ikeda, M Kamada, T Touge, K Deguchi, T Masaki Rinsho Shinkeigaku= Clinical Neurology 53 (5), 362-366, 2013 | 9 | 2013 |
| Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia Y Tada, K Kume, Y Matsuda, T Kurashige, Y Kanaya, R Ohsawa, ... Journal of Human Genetics 65 (4), 363-369, 2020 | 8 | 2020 |
| Retinitis pigmentosa prior to familial ALS caused by a homozygous cilia and flagella-associated protein 410 mutation T Kurashige, H Morino, Y Matsuda, T Mukai, T Murao, M Toko, K Kume, ... Journal of Neurology, Neurosurgery & Psychiatry 91 (2), 220-222, 2020 | 8 | 2020 |
