論文- 北本 哲之 -
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件数:234件
[2018]
1.Autopsied case of non-plaque-type dura mater graft-associated Creutzfeldt-Jakob disease presenting with extensive amyloid-β deposition..[Neuropathology : official journal of the Japanese Society of Neuropathology,38(5),(2018),549-556]Iwasaki Y, Imamura K, Iwai K, Kobayashi Y, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M
10.1111/neup.12503
http://www.ncbi.nlm.nih.gov/pubmed/30084170
2.Autopsy case of V180I genetic Creutzfeldt-Jakob disease presenting with early disease pathology..[Neuropathology : official journal of the Japanese Society of Neuropathology,(2018)]Iwasaki Y, Kato H, Ando T, Akagi A, Mimuro M, Miyahara H, Kitamoto T, Yoshida M
10.1111/neup.12516
http://www.ncbi.nlm.nih.gov/pubmed/30216556
3.An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid..[Brain and behavior,(2018),e1117-]Ishizawa K, Mitsufuji T, Shioda K, Kobayashi A, Komori T, Nakazato Y, Kitamoto T, Araki N, Yamamoto T, Sasaki A
10.1002/brb3.1117
http://www.ncbi.nlm.nih.gov/pubmed/30240140
4.PrP<sup>res</sup> deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD)..[Acta neuropathologica communications,6(1),(2018),78-]Takao M, Kimura H, Kitamoto T, Mihara B
10.1186/s40478-018-0582-5
http://www.ncbi.nlm.nih.gov/pubmed/30097055
5.A domain responsible for spontaneous conversion of bank vole prion protein..[Brain pathology (Zurich, Switzerland),(2018)]Kobayashi A, Matsuura Y, Takeuchi A, Yamada M, Miyoshi I, Mohri S, Kitamoto T
10.1111/bpa.12638
http://www.ncbi.nlm.nih.gov/pubmed/30051525
6.Neuroimaging-pathological correlations of [<sup>18</sup>F]THK5351 PET in progressive supranuclear palsy..[Acta neuropathologica communications,6(1),(2018),53-]Ishiki A, Harada R, Kai H, Sato N, Totsune T, Tomita N, Watanuki S, Hiraoka K, Ishikawa Y, Funaki Y, Iwata R, Furumoto S, Tashiro M, Sasano H, Kitamoto T, Kudo Y, Yanai K, Furukawa K, Okamura N, Arai H
10.1186/s40478-018-0556-7
http://www.ncbi.nlm.nih.gov/pubmed/29958546
7.Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review..[BMC neurology,18(1),(2018),54-]Miyake K, Hara T, Oshima E, Kawada K, Ishizu H, Yamauchi Y, Satoh K, Kitamoto T, Takenoshita S, Terada S, Yamada N
10.1186/s12883-018-1055-y
http://www.ncbi.nlm.nih.gov/pubmed/29699515
8.Correlations of <sup>18</sup>F-THK5351 PET with Postmortem Burden of Tau and Astrogliosis in Alzheimer Disease..[Journal of nuclear medicine : official publication, Society of Nuclear Medicine,59(4),(2018),671-674]Harada R, Ishiki A, Kai H, Sato N, Furukawa K, Furumoto S, Tago T, Tomita N, Watanuki S, Hiraoka K, Ishikawa Y, Funaki Y, Nakamura T, Yoshikawa T, Iwata R, Tashiro M, Sasano H, Kitamoto T, Yanai K, Arai H, Kudo Y, Okamura N
10.2967/jnumed.117.197426
http://www.ncbi.nlm.nih.gov/pubmed/28864633
9.Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases..[Neuroscience letters,668,(2018),43-47]Munesue Y, Shimazaki T, Qi Z, Isoda N, Sawa H, Aoshima K, Kimura T, Mohri S, Kitamoto T, Kobayashi A
10.1016/j.neulet.2018.01.014
http://www.ncbi.nlm.nih.gov/pubmed/29329906
10.Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene..[Biochemical and biophysical research communications,496(4),(2018),1055-1061]Ito Y, Sanjo N, Hizume M, Kobayashi A, Ohgami T, Satoh K, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T
10.1016/j.bbrc.2018.01.119
http://www.ncbi.nlm.nih.gov/pubmed/29382530
11.Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation..[Prion,12(1),(2018),54-62]Akagi A, Iwasaki Y, Mimuro M, Kitamoto T, Yamada M, Yoshida M
10.1080/19336896.2017.1414130
http://www.ncbi.nlm.nih.gov/pubmed/29264994
12.Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study..[Acta neuropathologica communications,6(1),(2018),5-]Cali I, Cohen ML, Haik S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, Maddox RA, Tagliavini F, Pocchiari M, Leschek E, Appleby BS, Safar JG, Schonberger LB, Gambetti P
10.1186/s40478-017-0503-z
http://www.ncbi.nlm.nih.gov/pubmed/29310723
13.Iatrogenic Creutzfeldt-Jakob disease..[Handbook of clinical neurology,153,(2018),207-218]Kobayashi A, Kitamoto T, Mizusawa H
10.1016/B978-0-444-63945-5.00012-X
http://www.ncbi.nlm.nih.gov/pubmed/29887137
[2017]
14.An autopsy case of Creutzfeldt-Jakob disease with a prion protein gene codon 180 mutation presenting with pathological laughing and an exaggerated startle reaction..[Neuropathology : official journal of the Japanese Society of Neuropathology,37(6),(2017),575-581]Iwasaki Y, Mori K, Ito M, Akagi A, Mimuro M, Kitamoto T, Yoshida M
10.1111/neup.12399
http://www.ncbi.nlm.nih.gov/pubmed/28703419
15.Clinical findings of a probable case of MM2-cortical-type sporadic Creutzfeldt-Jakob disease with antibodies to anti-N-terminus of α-enolase..[Prion,11(6),(2017),454-464]Hayashi Y, Yamada M, Kimura A, Asano T, Satoh K, Kitamoto T, Yoneda M, Inuzuka T
10.1080/19336896.2017.1377876
http://www.ncbi.nlm.nih.gov/pubmed/28967811
16.MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration and early pathologic indicators..[Neuropathology : official journal of the Japanese Society of Neuropathology,37(5),(2017),420-425]Iwasaki Y, Kato H, Ando T, Mimuro M, Kitamoto T, Yoshida M
10.1111/neup.12379
http://www.ncbi.nlm.nih.gov/pubmed/28402042
17.Protective Effect of Val<sub>129</sub>-PrP against Bovine Spongiform Encephalopathy but not Variant Creutzfeldt-Jakob Disease..[Emerging infectious diseases,23(9),(2017),1522-1530]Fernández-Borges N, Espinosa JC, Marín-Moreno A, Aguilar-Calvo P, Asante EA, Kitamoto T, Mohri S, Andréoletti O, Torres JM
10.3201/eid2309.161948
http://www.ncbi.nlm.nih.gov/pubmed/28820136
18.An autopsy-verified case of steroid-responsive encephalopathy with convulsion and a false-positive result from the real-time quaking-induced conversion assay..[Prion,11(4),(2017),284-292]Hayashi Y, Iwasaki Y, Yoshikura N, Asano T, Mimuro M, Kimura A, Satoh K, Kitamoto T, Yoshida M, Inuzuka T
10.1080/19336896.2017.1345416
http://www.ncbi.nlm.nih.gov/pubmed/28749249
19.An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques..[Neuropathology : official journal of the Japanese Society of Neuropathology,37(3),(2017),241-248]Iwasaki Y, Saito Y, Aiba I, Kobayashi A, Mimuro M, Kitamoto T, Yoshida M
10.1111/neup.12350
http://www.ncbi.nlm.nih.gov/pubmed/28568896
20.An autopsied case of MM1 + MM2-cortical with thalamic-type sporadic Creutzfeldt-Jakob disease presenting with hyperintensities on diffusion-weighted MRI before clinical onset..[Neuropathology : official journal of the Japanese Society of Neuropathology,37(1),(2017),78-85]Iwasaki Y, Mori K, Ito M, Mimuro M, Kitamoto T, Yoshida M
10.1111/neup.12327
http://www.ncbi.nlm.nih.gov/pubmed/27436355
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