Clinicopathological features of adult-onset neuronal intranuclear inclusion disease J Sone, K Mori, T Inagaki, R Katsumata, S Takagi, S Yokoi, K Araki, T Kato, ... Brain 139 (12), 3170-3186, 2016 | 317 | 2016 |
Statins and myotoxic effects associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase autoantibodies: an observational study in Japan Y Watanabe, S Suzuki, H Nishimura, K Murata, T Kurashige, M Ikawa, ... Medicine 94 (4), e416, 2015 | 105 | 2015 |
Immunopositivity for ESCRT-III subunit CHMP2B in granulovacuolar degeneration of neurons in the Alzheimer's disease hippocampus Y Yamazaki, T Takahashi, M Hiji, T Kurashige, Y Izumi, T Yamawaki, ... Neuroscience letters 477 (2), 86-90, 2010 | 64 | 2010 |
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patients T Yamamoto, H Sato, P San Lai, DK Nurputra, NIF Harahap, S Morikawa, ... Brain and Development 36 (10), 914-920, 2014 | 50 | 2014 |
Granulovacuolar degenerations appear in relation to hippocampal phosphorylated tau accumulation in various neurodegenerative disorders Y Yamazaki, T Matsubara, T Takahashi, T Kurashige, E Dohi, M Hiji, ... PLoS One 6 (11), e26996, 2011 | 43 | 2011 |
Synphilin-1 has neuroprotective effects on MPP+-induced Parkinson’s disease model cells by inhibiting ROS production and apoptosis T Shishido, Y Nagano, M Araki, T Kurashige, H Obayashi, T Nakamura, ... Neuroscience letters 690, 145-150, 2019 | 40 | 2019 |
Clinicopathologic features of oculopharyngodistal myopathy with LRP12 CGG repeat expansions compared with other oculopharyngodistal myopathy subtypes T Kumutpongpanich, M Ogasawara, A Ozaki, H Ishiura, S Tsuji, N Minami, ... JAMA neurology 78 (7), 853-863, 2021 | 32 | 2021 |
Phosphatidylinositol‐4, 5‐bisphosphate is enriched in granulovacuolar degeneration bodies and neurofibrillary tangles T Nishikawa, T Takahashi, M Nakamori, Y Yamazaki, T Kurashige, ... Neuropathology and applied neurobiology 40 (4), 489-501, 2014 | 32 | 2014 |
Detecting gene mutations in Japanese Alzheimer's patients by semiconductor sequencing R Yagi, R Miyamoto, H Morino, Y Izumi, M Kuramochi, T Kurashige, ... Neurobiology of Aging 35 (7), 1780. e1-1780. e5, 2014 | 28 | 2014 |
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 | 24 | 2021 |
Localization of CHMP2B‐immunoreactivity in the brainstem of Lewy body disease T Kurashige, T Takahashi, Y Yamazaki, M Hiji, Y Izumi, T Yamawaki, ... Neuropathology 33 (3), 237-245, 2013 | 24 | 2013 |
A mutant MATR3 mouse model to explain multisystem proteinopathy X Zhang, S Yamashita, K Hara, T Doki, N Tawara, T Ikeda, Y Misumi, ... The Journal of pathology 249 (2), 182-192, 2019 | 23 | 2019 |
Elevated urinary β2 microglobulin in the first identified Japanese family afflicted by X-linked myopathy with excessive autophagy T Kurashige, T Takahashi, Y Yamazaki, Y Nagano, K Kondo, T Nakamura, ... Neuromuscular Disorders 23 (11), 911-916, 2013 | 21 | 2013 |
Cyclin-dependent kinase 5 immunoreactivity for granulovacuolar degeneration M Nakamori, T Takahashi, Y Yamazaki, T Kurashige, T Yamawaki, ... Neuroreport 23 (15), 867-872, 2012 | 20 | 2012 |
TDP-43 Accumulation Within Intramuscular Nerve Bundles of Patients With Amyotrophic Lateral Sclerosis T Kurashige, H Morino, T Murao, Y Izumi, T Sugiura, K Kuraoka, ... JAMA Neurology 79 (7), 693-701, 2022 | 19 | 2022 |
A case of MELAS with G13513A mutation presenting with chronic kidney disease long before stroke-like episodes. A Motoda, T Kurashige, T Sugiura, T Nakamura, T Yamawaki, K Arihiro, ... Rinsho shinkeigaku= Clinical neurology 53 (6), 446-451, 2013 | 19 | 2013 |
Anti-HMGCR myopathy: clinical and histopathological features, and prognosis T Kurashige Current Opinion in Rheumatology 33 (6), 554-562, 2021 | 18 | 2021 |
Anti-HMGCR antibody-positive myopathy shows Bcl-2-positive inflammation and lymphocytic accumulations T Kurashige, T Murao, N Mine, T Sugiura, Y Inazuka, K Kuraoka, ... Journal of Neuropathology & Experimental Neurology 79 (4), 448-457, 2020 | 18 | 2020 |
Compound heterozygote mutations in the SIGMAR1 gene in an oldest-old patient with amyotrophic lateral sclerosis S FUS | 18 | 2018 |
Optineurin defects cause TDP43-pathology with autophagic vacuolar formation Takashi Kurashige, Masahito Kuramochi, Ryosuke Ohsawa, Yui Yamashita, Go ... Neurobiology of Disease, https://doi.org/10.1016/j.nbd.2020.10521, 2020 | 16* | 2020 |