| Anthocyanin suppresses the toxicity of Aβ deposits through diversion of molecular forms in in vitro and in vivo models of Alzheimer's disease MY Yamakawa, K Uchino, Y Watanabe, T Adachi, M Nakanishi, H Ichino, ... Nutritional Neuroscience 19 (1), 32-42, 2016 | 73 | 2016 |
| Neuropathological asymmetry in argyrophilic grain disease T Adachi, Y Saito, H Hatsuta, S Funabe, AM Tokumaru, K Ishii, T Arai, ... Journal of Neuropathology & Experimental Neurology 69 (7), 737-744, 2010 | 48 | 2010 |
| Tau and TDP-43 accumulation of the basal nucleus of Meynert in individuals with cerebral lobar infarcts or hemorrhage H Hatsuta, M Takao, A Nogami, A Uchino, H Sumikura, T Takata, ... Acta Neuropathologica Communications 7, 1-11, 2019 | 37 | 2019 |
| Ultrastructural and biochemical classification of pathogenic tau, α-synuclein and TDP-43 A Tarutani, T Adachi, H Akatsu, Y Hashizume, K Hasegawa, Y Saito, ... Acta neuropathologica 143 (6), 613-640, 2022 | 35 | 2022 |
| Epidemiological survey of frontotemporal lobar degeneration in tottori prefecture, Japan K Wada-Isoe, S Ito, T Adachi, M Yamawaki, S Nakashita, M Kusumi, ... Dementia and geriatric cognitive disorders extra 2 (1), 381-386, 2012 | 21 | 2012 |
| Autopsy case of spinocerebellar ataxia type 31 with severe dementia at the terminal stage T Adachi, M Kitayama, T Nakano, Y Adachi, S Kato, K Nakashima Neuropathology 35 (3), 273-279, 2015 | 20 | 2015 |
| Cowden syndrome with a novel PTEN mutation presenting with partial epilepsy related to focal cortical dysplasia T Adachi, H Takigawa, T Nomura, Y Watanabe, H Kowa Internal Medicine 57 (1), 97-99, 2018 | 18 | 2018 |
| Clinical and mutational spectrum of Japanese patients with recessive variants in SH3TC2 JH Yuan, A Hashiguchi, Y Okamoto, A Yoshimura, M Ando, K Shiomi, ... Journal of Human Genetics 63 (3), 281-287, 2018 | 10 | 2018 |
| Japanese version of the ALS-FTD-Questionnaire (ALS-FTD-QJ) Y Watanabe, E Beeldman, J Raaphorst, Y Izumi, H Yoshino, M Masuda, ... Journal of the neurological sciences 367, 51-55, 2016 | 9 | 2016 |
| A single-institution study on predictors of short-term progression from mild cognitive impairment in Parkinson’s disease to Parkinson’s disease with dementia Y Tajiri, K Wada-Isoe, K Tanaka, T Adachi, R Hanajima, K Nakashima Yonago Acta Medica 63 (1), 28-33, 2020 | 6 | 2020 |
| First Japanese autopsy case showing LRRK2 mutation G2019S and TDP-43 proteinopathy M Sakuwa, T Adachi, Y Suzuki, K Yoshida, H Fukuda, H Miura, Y Adachi, ... Parkinsonism & Related Disorders 91, 85-87, 2021 | 5 | 2021 |
| Neuropathy/intranuclear inclusion bodies in oculopharyngodistal myopathy: A case report T Matsubara, Y Saito, T Kurashige, M Higashihara, F Hasegawa, ... Eneurologicalsci 24, 2021 | 4 | 2021 |
| A case of sporadic late-onset nemaline myopathy associated with myasthenia gravis positive for anti-titin antibody and anti-Kv1. 4 antibody M Kanatani, T Adachi, R Sakata, Y Watanabe, R Hanajima Rinsho Shinkeigaku= Clinical Neurology 60 (7), 489-494, 2020 | 4 | 2020 |
| Anti-myelin oligodendrocyte glycoprotein antibodies in a patient with recurrent optic neuritis involving the cerebral white matter and brainstem T Adachi, K Yasui, T Takahashi, K Fujihara, Y Watanabe, K Nakashima Internal Medicine 55 (10), 1351-1354, 2016 | 4 | 2016 |
| First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing Y Miyamoto, T Okazaki, K Watanabe, M Togawa, T Adachi, A Kato, ... Brain and Development 45 (1), 70-76, 2023 | 3 | 2023 |
| Cerebral venous thrombosis due to nontyphoidal salmonella bacteremia K Taneda, T Adachi, Y Watanabe, R Hanajima Internal Medicine 58 (13), 1943-1946, 2019 | 3 | 2019 |
| Non-lesional skin biopsy for a diagnosis of neuronal intranuclear inclusion disease. A Ito, Y Yoshida, K Adachi, T Adachi, O Yamamoto The Journal of Dermatology 45 (4), e67-e67, 2017 | 3 | 2017 |
| Autopsy-confirmed progressive supranuclear palsy with decreased uptake of metaiodobenzylguanidine T Adachi, M Kitayama, K Wada-Isoe, T Nakano, K Nakashima Clinical Neurology and Neurosurgery 115 (8), 1555-1557, 2013 | 3 | 2013 |
| An autopsy case of PARK2 due to a homozygous exon 2 deletion of parkin and associated with α‐synucleinopathy M Sakuwa, T Adachi, K Yoshida, Y Adachi, T Nakano, R Hanajima Neuropathology 41 (4), 293-300, 2021 | 2 | 2021 |
| Alpha-synuclein accumulation in a patient with Auerbach's plexus of pure autonomic failure T Kurashiki-Osaka, T Adachi, H Nakayasu, K Nakashima Internal Medicine 53 (19), 2261-2261, 2014 | 2 | 2014 |
