Shigetoshi Kuroda, MD
Affiliations: | Psychiatry | Okayama University, Okayama-shi, Okayama-ken, Japan |
Website:
http://www.labome.org/expert/japan/okayama/kuroda/shigetoshi-kuroda-523650.htmlGoogle:
"Shigetoshi Kuroda"Bio:
http://www.curehunter.com/public/authorSummary-Kuroda,%20Shigetoshi.do
http://onlinelibrary.wiley.com/doi/10.1111/j.1440-1819.1975.tb02321.x/abstract
Mean distance: 19.07 (cluster 24) | S | N | B | C | P |
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Publications
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| Takeuchi A, Mohri S, Kai H, et al. (2019) Two distinct prions in fatal familial insomnia and its sporadic form. Brain Communications. 1: fcz045 |
| Miki T, Yokota O, Takenoshita S, et al. (2017) Frontotemporal lobar degeneration due to P301L tau mutation showing apathy and severe frontal atrophy but lacking other behavioral changes: A case report and literature review. Neuropathology : Official Journal of the Japanese Society of Neuropathology |
| Yokota O, Miki T, Ikeda C, et al. (2017) Neuropathological comorbidity associated with argyrophilic grain disease. Neuropathology : Official Journal of the Japanese Society of Neuropathology |
| Miki T, Yokota O, Ishizu H, et al. (2016) Behavioral variant of frontotemporal dementia: Fundamental clinical issues associated with prediction of pathological bases. Neuropathology : Official Journal of the Japanese Society of Neuropathology |
| Nagao S, Yokota O, Ikeda C, et al. (2014) Argyrophilic grain disease as a neurodegenerative substrate in late-onset schizophrenia and delusional disorders. European Archives of Psychiatry and Clinical Neuroscience. 264: 317-31 |
| Haraguchi T, Terada S, Ishizu H, et al. (2011) Coexistence of TDP-43 and tau pathology in neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome). Neuropathology : Official Journal of the Japanese Society of Neuropathology. 31: 531-9 |
| Nozaki I, Hamaguchi T, Sanjo N, et al. (2010) Prospective 10-year surveillance of human prion diseases in Japan. Brain : a Journal of Neurology. 133: 3043-57 |
| Fu YJ, Nishihira Y, Kuroda S, et al. (2010) Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity. Acta Neuropathologica. 120: 21-32 |
| Yoshida H, Terada S, Ishizu H, et al. (2010) An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 30: 159-64 |
| Munoz DG, Neumann M, Kusaka H, et al. (2009) FUS pathology in basophilic inclusion body disease. Acta Neuropathologica. 118: 617-27 |