| Year |
Citation |
Score |
| 2019 |
Takeuchi A, Mohri S, Kai H, Tamaoka A, Kobayashi A, Mizusawa H, Iwasaki Y, Yoshida M, Shimizu H, Murayama S, Kuroda S, Morita M, Parchi P, Kitamoto T. Two distinct prions in fatal familial insomnia and its sporadic form. Brain Communications. 1: fcz045. PMID 32954274 DOI: 10.1093/braincomms/fcz045 |
0.401 |
|
| 2017 |
Miki T, Yokota O, Takenoshita S, Mori Y, Yamazaki K, Ozaki Y, Ueno SI, Haraguchi T, Ishizu H, Kuroda S, Terada S, Yamada N. 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. PMID 29105852 DOI: 10.1111/Neup.12441 |
0.332 |
|
| 2017 |
Yokota O, Miki T, Ikeda C, Nagao S, Takenoshita S, Ishizu H, Haraguchi T, Kuroda S, Terada S, Yamada N. Neuropathological comorbidity associated with argyrophilic grain disease. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 28906054 DOI: 10.1111/Neup.12429 |
0.338 |
|
| 2016 |
Miki T, Yokota O, Ishizu H, Kuroda S, Oshima E, Terada S, Yamada N. Behavioral variant of frontotemporal dementia: Fundamental clinical issues associated with prediction of pathological bases. Neuropathology : Official Journal of the Japanese Society of Neuropathology. PMID 26969837 DOI: 10.1111/Neup.12290 |
0.316 |
|
| 2014 |
Nagao S, Yokota O, Ikeda C, Takeda N, Ishizu H, Kuroda S, Sudo K, Terada S, Murayama S, Uchitomi Y. Argyrophilic grain disease as a neurodegenerative substrate in late-onset schizophrenia and delusional disorders. European Archives of Psychiatry and Clinical Neuroscience. 264: 317-31. PMID 24272318 DOI: 10.1007/S00406-013-0472-6 |
0.324 |
|
| 2011 |
Haraguchi T, Terada S, Ishizu H, Yokota O, Yoshida H, Takeda N, Kishimoto Y, Katayama N, Takata H, Akagi M, Kuroda S, Ihara Y, Uchitomi Y. 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. PMID 21276079 DOI: 10.1111/J.1440-1789.2010.01186.X |
0.338 |
|
| 2010 |
Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, ... ... Kuroda S, et al. Prospective 10-year surveillance of human prion diseases in Japan. Brain : a Journal of Neurology. 133: 3043-57. PMID 20855418 DOI: 10.1093/Brain/Awq216 |
0.485 |
|
| 2010 |
Fu YJ, Nishihira Y, Kuroda S, Toyoshima Y, Ishihara T, Shinozaki M, Miyashita A, Piao YS, Tan CF, Tani T, Koike R, Iwanaga K, Tsujihata M, Onodera O, Kuwano R, et al. 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. PMID 20140439 DOI: 10.1007/S00401-010-0649-2 |
0.364 |
|
| 2010 |
Yoshida H, Terada S, Ishizu H, Ikeda K, Hayabara T, Ikeda K, Deguchi K, Touge T, Kitamoto T, Kuroda S. 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. PMID 19703264 DOI: 10.1111/J.1440-1789.2009.01048.X |
0.34 |
|
| 2009 |
Munoz DG, Neumann M, Kusaka H, Yokota O, Ishihara K, Terada S, Kuroda S, Mackenzie IR. FUS pathology in basophilic inclusion body disease. Acta Neuropathologica. 118: 617-27. PMID 19830439 DOI: 10.1007/S00401-009-0598-9 |
0.561 |
|
| 2009 |
Yokota O, Tsuchiya K, Arai T, Yagishita S, Matsubara O, Mochizuki A, Tamaoka A, Kawamura M, Yoshida H, Terada S, Ishizu H, Kuroda S, Akiyama H. Clinicopathological characterization of Pick's disease versus frontotemporal lobar degeneration with ubiquitin/TDP-43-positive inclusions. Acta Neuropathologica. 117: 429-44. PMID 19194716 DOI: 10.1007/S00401-009-0493-4 |
0.337 |
|
| 2009 |
Haraguchi T, Terada S, Ishizu H, Sakai K, Tanabe Y, Nagai T, Takata H, Nobukuni K, Ihara Y, Kitamoto T, Kuroda S. Coexistence of Creutzfeldt-Jakob disease, Lewy body disease, and Alzheimer's disease pathology: an autopsy case showing typical clinical features of Creutzfeldt-Jakob disease. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 29: 454-9. PMID 18715272 DOI: 10.1111/J.1440-1789.2008.00964.X |
0.335 |
|
| 2008 |
Yokota O, Tsuchiya K, Terada S, Ishizu H, Uchikado H, Ikeda M, Oyanagi K, Nakano I, Murayama S, Kuroda S, Akiyama H. Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study. Acta Neuropathologica. 115: 561-75. PMID 18080129 DOI: 10.1007/S00401-007-0329-Z |
0.505 |
|
| 2007 |
Shiga Y, Satoh K, Kitamoto T, Kanno S, Nakashima I, Sato S, Fujihara K, Takata H, Nobukuni K, Kuroda S, Takano H, Umeda Y, Konno H, Nagasato K, Satoh A, et al. Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution. Journal of Neurology. 254: 1509-17. PMID 17965961 DOI: 10.1007/S00415-007-0540-9 |
0.484 |
|
| 2007 |
Shibata N, Kawaguchi M, Uchida K, Kakita A, Takahashi H, Nakano R, Fujimura H, Sakoda S, Ihara Y, Nobukuni K, Takehisa Y, Kuroda S, Kokubo Y, Kuzuhara S, Honma T, et al. Protein-bound crotonaldehyde accumulates in the spinal cord of superoxide dismutase-1 mutation-associated familial amyotrophic lateral sclerosis and its transgenic mouse model. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 27: 49-61. PMID 17319283 DOI: 10.1111/J.1440-1789.2006.00746.X |
0.699 |
|
| 2007 |
Yokota O, Tsuchiya K, Uchihara T, Ujike H, Terada S, Takahashi M, Kimura Y, Ishizu H, Akiyama H, Kuroda S. Lewy body variant of Alzheimer's disease or cerebral type lewy body disease? Two autopsy cases of presenile onset with minimal involvement of the brainstem. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 27: 21-35. PMID 17319280 DOI: 10.1111/J.1440-1789.2006.00736.X |
0.348 |
|
| 2006 |
Ujike H, Sakai A, Nakata K, Tanaka Y, Kodaka T, Okahisa Y, Harano M, Inada T, Yamada M, Komiyama T, Hori T, Sekine Y, Iwata N, Sora I, Iyo M, ... ... Kuroda S, et al. Association study of the dihydropyrimidinase-related protein 2 gene and methamphetamine psychosis. Annals of the New York Academy of Sciences. 1074: 90-6. PMID 17105906 DOI: 10.1196/Annals.1369.008 |
0.3 |
|
| 2006 |
Yokota O, Tsuchiya K, Oda T, Ishihara T, de Silva R, Lees AJ, Arai T, Uchihara T, Ishizu H, Kuroda S, Akiyama H. Amyotrophic lateral sclerosis with dementia: an autopsy case showing many Bunina bodies, tau-positive neuronal and astrocytic plaque-like pathologies, and pallido-nigral degeneration. Acta Neuropathologica. 112: 633-45. PMID 17021751 DOI: 10.1007/S00401-006-0141-1 |
0.339 |
|
| 2006 |
Yokota O, Fujisawa Y, Takahashi J, Terada S, Ishihara T, Nakashima H, Oshima E, Kugo A, Ata T, Ishizu H, Kuroda S, Sasaki K. Effects of group-home care on behavioral symptoms, quality of life, and psychotropic drug use in patients with frontotemporal dementia. Journal of the American Medical Directors Association. 7: 335-7. PMID 16765875 DOI: 10.1016/J.Jamda.2006.02.012 |
0.379 |
|
| 2005 |
Yokota O, Sasaki K, Fujisawa Y, Takahashi J, Terada S, Ishihara T, Nakashima H, Kugo A, Ata T, Ishizu H, Kuroda S. Frequency of early and late-onset dementias in a Japanese memory disorders clinic. European Journal of Neurology. 12: 782-790. PMID 16190916 DOI: 10.1111/J.1468-1331.2005.01072.X |
0.304 |
|
| 2005 |
Hamaguchi T, Kitamoto T, Sato T, Mizusawa H, Nakamura Y, Noguchi M, Furukawa Y, Ishida C, Kuji I, Mitani K, Murayama S, Kohriyama T, Katayama S, Yamashita M, Yamamoto T, ... ... Kuroda S, et al. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease. Neurology. 64: 643-8. PMID 15728285 DOI: 10.1212/01.Wnl.0000151847.57956.Fa |
0.486 |
|
| 2004 |
Oka T, Hamamura T, Lee Y, Miyata S, Habara T, Endo S, Taoka H, Kuroda S. Atypical properties of several classes of antipsychotic drugs on the basis of differential induction of Fos-like immunoreactivity in the rat brain. Life Sciences. 76: 225-37. PMID 15519367 DOI: 10.1016/J.Lfs.2004.08.009 |
0.302 |
|
| 2004 |
Terada S, Ishizu H, Yokota O, Ishihara T, Nakashima H, Kugo A, Tanaka Y, Nakashima T, Nakashima Y, Kuroda S. An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease. Acta Neuropathologica. 108: 538-45. PMID 15365727 DOI: 10.1007/S00401-004-0920-5 |
0.307 |
|
| 2004 |
Yokota O, Terada S, Ishihara T, Nakashima H, Kugo A, Ujike H, Tsuchiya K, Ikeda K, Saito Y, Murayama S, Ishizu H, Kuroda S. Neuronal expression of cyclooxygenase-2, a pro-inflammatory protein, in the hippocampus of patients with schizophrenia. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 28: 715-21. PMID 15276698 DOI: 10.1016/J.Pnpbp.2004.05.018 |
0.312 |
|
| 2004 |
Kobayashi K, Hayashi M, Kidani T, Ujike H, Iijima M, Ishihara T, Nakano H, Sugimori K, Shimazaki M, Kuroda S, Koshino Y. Pick's disease pathology of a missense mutation of S305N of frontotemporal dementia and parkinsonism linked to chromosome 17: another phenotype of S305N. Dementia and Geriatric Cognitive Disorders. 17: 293-7. PMID 15178939 DOI: 10.1159/000077157 |
0.322 |
|
| 2004 |
Yokota O, Terada S, Ishizu H, Ishihara T, Nakashima H, Kugo A, Tsuchiya K, Ikeda K, Hayabara T, Saito Y, Murayama S, Uéda K, Checler F, Kuroda S. Increased expression of neuronal cyclooxygenase-2 in the hippocampus in amyotrophic lateral sclerosis both with and without dementia. Acta Neuropathologica. 107: 399-405. PMID 14991384 DOI: 10.1007/S00401-004-0826-2 |
0.315 |
|
| 2004 |
Sakai A, Ujike H, Nakata K, Takehisa Y, Imamura T, Uchida N, Kanzaki A, Yamamoto M, Fujisawa Y, Okumura K, Kuroda S. Association of the Neprilysin gene with susceptibility to late-onset Alzheimer's disease. Dementia and Geriatric Cognitive Disorders. 17: 164-9. PMID 14739539 DOI: 10.1159/000076351 |
0.302 |
|
| 2003 |
Yokota O, Terada S, Ishizu H, Ujike H, Ishihara T, Namba M, Hayashi Y, Nishinaka T, Namba R, Nakashima H, Uéda K, Checler F, Kuroda S. Variability and heterogeneity in Alzheimer's disease with cotton wool plaques: a clinicopathological study of four autopsy cases. Acta Neuropathologica. 106: 348-56. PMID 12883830 DOI: 10.1007/S00401-003-0737-7 |
0.312 |
|
| 2003 |
Yokota O, Terada S, Ishizu H, Ishihara T, Ujike H, Nakashima H, Nakashima Y, Kugo A, Checler F, Kuroda S. Cyclooxygenase-2 in the hippocampus is up-regulated in Alzheimer's disease but not in variant Alzheimer's disease with cotton wool plaques in humans. Neuroscience Letters. 343: 175-9. PMID 12770691 DOI: 10.1016/S0304-3940(03)00339-2 |
0.308 |
|
| 2003 |
Terada S, Ishizu H, Yokota O, Tsuchiya K, Nakashima H, Ishihara T, Fujita D, Uéda K, Ikeda K, Kuroda S. Glial involvement in diffuse Lewy body disease. Acta Neuropathologica. 105: 163-9. PMID 12536227 DOI: 10.1007/S00401-002-0622-9 |
0.308 |
|
| 2002 |
Yokota O, Terada S, Ishizu H, Ujike H, Ishihara T, Nakashima H, Yasuda M, Kitamura Y, Uéda K, Checler F, Kuroda S. NACP/alpha-synuclein, NAC, and beta-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases. Acta Neuropathologica. 104: 637-48. PMID 12410385 DOI: 10.1007/S00401-002-0596-7 |
0.309 |
|
| 2002 |
Tabira T, Chui DH, Nakayama H, Kuroda S, Shibuya M. Alzheimer's disease with spastic paresis and cotton wool type plaques. Journal of Neuroscience Research. 70: 367-72. PMID 12391599 DOI: 10.1002/Jnr.10392 |
0.311 |
|
| 2002 |
Yokota O, Terada S, Ishizu H, Tsuchiya K, Kitamura Y, Ikeda K, Uéda K, Kuroda S. NACP/alpha-synuclein immunoreactivity in diffuse neurofibrillary tangles with calcification (DNTC). Acta Neuropathologica. 104: 333-41. PMID 12200618 DOI: 10.1007/S00401-002-0545-5 |
0.329 |
|
| 2002 |
Yokota O, Ishizu H, Terada S, Tsuchiya K, Haraguchi T, Nose S, Kawai K, Ikeda K, Kuroda S. Preservation of nigral neurons in Pick's disease with Pick bodies: a clinicopathological and morphometric study of five autopsy cases. Journal of the Neurological Sciences. 194: 41-8. PMID 11809165 DOI: 10.1016/S0022-510X(01)00671-2 |
0.321 |
|
| 2001 |
Terada S, Ishizu H, Tanabe Y, Takehisa Y, Haraguchi T, Hamaya K, Nose S, Sudo K, Kuroda S. Plaque-like structures and arteriosclerotic changes in "diffuse neurofibrillary tangles with calcification" (DNTC) Acta Neuropathologica. 102: 597-603. PMID 11761720 DOI: 10.1007/S004010100411 |
0.319 |
|
| 2001 |
Tsuchiya K, Ishizu H, Nakano I, Kita Y, Sawabe M, Haga C, Kuyama K, Nishinaka T, Oyanagi K, Ikeda K, Kuroda S. Distribution of basal ganglia lesions in generalized variant of Pick's disease: a clinicopathological study of four autopsy cases. Acta Neuropathologica. 102: 441-8. PMID 11699556 DOI: 10.1007/S004010100388 |
0.475 |
|
| 2001 |
Takehisa Y, Ujike H, Ishizu H, Terada S, Haraguchi T, Tanaka Y, Nishinaka T, Nobukuni K, Ihara Y, Namba R, Yasuda T, Nishibori M, Hayabara T, Kuroda S. Familial amyotrophic lateral sclerosis with a novel Leu126Ser mutation in the copper/zinc superoxide dismutase gene showing mild clinical features and lewy body-like hyaline inclusions. Archives of Neurology. 58: 736-40. PMID 11346368 DOI: 10.1001/Archneur.58.5.736 |
0.3 |
|
| 2001 |
Ujike H, Yamamoto M, Kanzaki A, Okumura K, Takaki M, Kuroda S. Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's disease. Movement Disorders. 16: 111-113. PMID 11215568 DOI: 10.1002/1531-8257(200101)16:1<111::Aid-Mds1023>3.0.Co;2-6 |
0.302 |
|
| 2001 |
Terada S, Ishizu H, Haraguchi T, Takehisa Y, Tanabe Y, Kawai K, Kuroda S. Tau-negative astrocytic star-like inclusions and coiled bodies in dementia with Lewy bodies. Acta Neuropathologica. 100: 464-8. PMID 11045667 DOI: 10.1007/S004010000213 |
0.312 |
|
| 2000 |
Haraguchi T, Ishizu H, Terada S, Takehisa Y, Tanabe Y, Nishinaka T, Kawai K, Kuroda S, Komoto Y, Namba M. An autopsy case of postencephalitic parkinsonism of von Economo type: Some new observations concerning neurofibrillary tangles and astrocytic tangles Neuropathology. 20: 143-148. PMID 10935451 DOI: 10.1046/J.1440-1789.2000.00287.X |
0.322 |
|
| 2000 |
Yasuda M, Maeda S, Kawamata T, Tamaoka A, Yamamoto Y, Kuroda S, Maeda K, Tanaka C. Novel presenilin-1 mutation with widespread cortical amyloid deposition but limited cerebral amyloid angiopathy Journal of Neurology, Neurosurgery, and Psychiatry. 68: 220-223. PMID 10644793 DOI: 10.1136/Jnnp.68.2.220 |
0.314 |
|
| 1999 |
Lee Y, Hamamura T, Ohashi K, Fujiwara Y, Kuroda S. The effect of lithium on methamphetamine-induced regional Fos protein expression in the rat brain. Neuroreport. 10: 895-900. PMID 10321456 DOI: 10.1097/00001756-199904060-00001 |
0.312 |
|
| 1999 |
Ishizu H, Tanabe Y, Tareda S, Takehisa Y, Haraguchi T, Nishinaka T, Kuroda S. Frontotemporal dementia: Pick type Neuropathology. 19: 422-432. DOI: 10.1046/J.1440-1789.1999.00262.X |
0.303 |
|
| 1998 |
Kodama M, Akiyama K, Ujike H, Shimizu Y, Tanaka Y, Kuroda S. A robust increase in expression of arc gene, an effector immediate early gene, in the rat brain after acute and chronic methamphetamine administration Brain Research. 796: 273-283. PMID 9689478 DOI: 10.1016/S0006-8993(98)00349-7 |
0.306 |
|
| 1994 |
Kawai K, Kuroda S, Watarai S, Takahashi H, Ikuta F. Occurrence of GD3 ganglioside in reactive astrocytes--an immunocytochemical study in the rat brain. Neuroscience Letters. 174: 225-7. PMID 7970185 DOI: 10.1016/0304-3940(94)90027-2 |
0.521 |
|
| 1987 |
Kuroda S, Otsuki S, Hayashi Y. Diffuse Lewy body disease: an autopsy case. Acta Medica Okayama. 41: 133-139. PMID 2820201 DOI: 10.18926/Amo/31770 |
0.325 |
|
| 1983 |
Kuroda S, Hirano A, Yuasa S. Adrenoleukodystrophy-cerebello-brainstem dominant case. Acta Neuropathologica. 60: 149-52. PMID 6880618 DOI: 10.1007/Bf00685361 |
0.513 |
|
| 1973 |
Ishino H, Kuroda S, Hayahara T, Otsuki S. An autopsy case of cerebral form of v. Winiwarter-Buerger's disease with a chronic course of 12 years. Psychiatry and Clinical Neurosciences. 27: 207-221. PMID 4800548 DOI: 10.1111/J.1440-1819.1973.Tb00098.X |
0.301 |
|
| 1972 |
Ishino H, Hirata J, Kuroda S, Otsuki S. An Autopsy Case of “Pseudo‐Ulegyric Type” of Hepatocerebral Disease Psychiatry and Clinical Neurosciences. 26: 45-53. PMID 5068471 DOI: 10.1111/J.1440-1819.1972.Tb01111.X |
0.332 |
|
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