Tetsuyuki Kitamoto

Tetsuyuki Kitamoto

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Tetsuyuki Kitamoto

Publications by authors named "Tetsuyuki Kitamoto"

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Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease.

J Neurol Sci 2019 Oct 22;408:116515. Epub 2019 Oct 22.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Yazakokarimata 1-1, Nagakute, Aichi, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2019.116515DOI Listing
October 2019

Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex.

Neuropathology 2019 Sep 12. Epub 2019 Sep 12.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12595DOI Listing
September 2019

Marchiafava-Bignami disease with haemophagocytic lymphohistiocytosis as a postoperative complication of cardiac surgery.

BMJ Case Rep 2019 Aug 26;12(8). Epub 2019 Aug 26.

Neurological Science, Tohoku University School of Medicine, Sendai, Miyagi, Japan.

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http://dx.doi.org/10.1136/bcr-2019-230368DOI Listing
August 2019

Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene.

Prion 2018 13;12(5-6):315-319. Epub 2018 Nov 13.

a Department of Neurology and Neurological Science , Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences , Yushima Bunkyo-ku , Tokyo , Japan.

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https://www.tandfonline.com/doi/full/10.1080/19336896.2018.1
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http://dx.doi.org/10.1080/19336896.2018.1541689DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277180PMC
July 2019

Age at onset in genetic prion disease and the design of preventive clinical trials.

Neurology 2019 Jul 6;93(2):e125-e134. Epub 2019 Jun 6.

From Broad Institute of MIT and Harvard (E.V.M., S.M.V.), Cambridge; Analytical and Translational Genetics Unit (E.V.M.), Massachusetts General Hospital; Program in Biological and Biomedical Sciences (E.V.M., S.M.V.), Harvard Medical School, Boston; Prion Alliance (E.V.M., S.M.V.), Cambridge; Harvard Business School (M.C.O.), Boston, MA; Institut du Cerveau et de la Moelle Épinière (J.-P.B., S.H.), ICM, Inserm U 1127, CNRS UMR 7225, Sorbonne Université; Cellule Nationale de Référence des Maladies de Creutzfeldt-Jakob (J.-P.B., S.H., J.-L.P.), Assistance Publique-Hôpitaux de Paris, France; National Reference Center for TSE (I.Z., C.P., P.H., T.K.), Georg-August University, Göttingen, Germany; IRCCS-Istituto delle Scienze Neurologiche di Bologna (P.P., S.C.); Departments of Experimental, Diagnostic and Specialty Medicine (P.P.) and Biomedical and Neuromotor Sciences (S.C.), University of Bologna, Italy; National Prion Disease Pathology Surveillance Center (J.S.), Case Western Reserve University, Cleveland, OH; MRC Prion Unit at UCL (J.K., S.M.), Institute of Prion Diseases, University College London, UK; Memory and Aging Center (J.C.F., L.T.T., M.D.G.), University of California San Francisco; Australian National CJD Registry (C.S., S.J.C.), University of Melbourne, Parkville, Australia; Department of Neurological Science (T.K.), Tohoku University Graduate School of Medicine, Sendai; Department of Public Health (R.A., Y.N.), Jichi Medical University, Shimotsuke; Department of Neurology and Neurobiology of Aging (T.H., M.Y.), Kanazawa University Graduate School of Medical Sciences, Kanazawa; Department of Neurology and Neurological Science (N.S.), Tokyo Medical and Dental University; National Center of Neurology and Psychiatry (T.T., H.M.), Kodaira, Japan; Laboratory of Prion Neurobiology (R.C.), Istituto di Ricerche Farmacologiche Mario Negri IRCCS, Milan; AULSS2 Ca' Foncello Hospital (I.R.), Treviso, Italy; Spanish National Reference Center for CJD (J.d.P.-C., M.C.), Instituto de Salud Carlos III and CIBERNED, Madrid, Spain; and NHS National Prion Clinic (S.M.), National Hospital for Neurology and Neurosurgery, UCL Hospitals NHS Foundation Trust, London, WC1N 3BG, UK.

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http://dx.doi.org/10.1212/WNL.0000000000007745DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6656649PMC
July 2019

Autopsied case of sporadic Creutzfeldt-Jakob disease classified as MM1+2C-type.

Neuropathology 2019 Jun 7;39(3):240-247. Epub 2019 May 7.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12557DOI Listing
June 2019

A domain responsible for spontaneous conversion of bank vole prion protein.

Brain Pathol 2019 03 29;29(2):155-163. Epub 2018 Oct 29.

Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1111/bpa.12638DOI Listing
March 2019

Intermolecular crosslinking of abnormal prion protein is efficiently induced by a primuline-sensitized photoreaction.

Biochim Biophys Acta Gen Subj 2019 02 14;1863(2):384-394. Epub 2018 Nov 14.

Department of Neurochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03044165183035
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http://dx.doi.org/10.1016/j.bbagen.2018.11.008DOI Listing
February 2019

Autopsy case of V180I genetic Creutzfeldt-Jakob disease presenting with early disease pathology.

Neuropathology 2018 Dec 14;38(6):638-645. Epub 2018 Sep 14.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://doi.wiley.com/10.1111/neup.12516
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http://dx.doi.org/10.1111/neup.12516DOI Listing
December 2018

[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].

Rinsho Shinkeigaku 2018 Nov 27;58(11):682-687. Epub 2018 Oct 27.

Division of CJD Science and Technology, Department of Prion Research, Center for Translational and Advanced Animal Research on Human Diseases, Tohoku University School of Medicine.

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http://dx.doi.org/10.5692/clinicalneurol.cn-001206DOI Listing
November 2018

Autopsied case of non-plaque-type dura mater graft-associated Creutzfeldt-Jakob disease presenting with extensive amyloid-β deposition.

Neuropathology 2018 Oct 6;38(5):549-556. Epub 2018 Aug 6.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12503DOI Listing
October 2018

Iatrogenic Creutzfeldt-Jakob disease.

Handb Clin Neurol 2018 ;153:207-218

National Center of Neurology and Psychiatry, Kodaira, Japan. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-63945-5.00012-XDOI Listing
September 2018

PrP deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD).

Acta Neuropathol Commun 2018 08 10;6(1):78. Epub 2018 Aug 10.

Department of Neurology and Brain Bank, Mihara Memorial Hospital, 366 Ohtemachi, Isesaki, Gunma, 372-0006, Japan.

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https://actaneurocomms.biomedcentral.com/articles/10.1186/s4
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http://dx.doi.org/10.1186/s40478-018-0582-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6086066PMC
August 2018

Neuroimaging-pathological correlations of [F]THK5351 PET in progressive supranuclear palsy.

Acta Neuropathol Commun 2018 06 29;6(1):53. Epub 2018 Jun 29.

Department of Geriatrics and Gerontology, Division of Brain Science, Institute of Development, Aging and Cancer, Tohoku University, 4-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi, Japan.

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http://dx.doi.org/10.1186/s40478-018-0556-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025736PMC
June 2018

Creutzfeldt-Jakob disease with Alzheimer pathology, presenting with status epilepticus following repeated partial seizures: a case report and literature review.

BMC Neurol 2018 Apr 25;18(1):54. Epub 2018 Apr 25.

Department of Psychiatry, Okayama University Graduate School of Medicine, Dentistry, and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Kita-ku, Okayama, 700-8558, Japan.

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http://dx.doi.org/10.1186/s12883-018-1055-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921414PMC
April 2018

Development of a quick bioassay for the evaluation of transmission properties of acquired prion diseases.

Neurosci Lett 2018 03 9;668:43-47. Epub 2018 Jan 9.

Laboratory of Comparative Pathology, Faculty of Veterinary Medicine, Hokkaido University, Kita 18 Nishi 9, Kita-ku, Sapporo, 060-0818, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.neulet.2018.01.014DOI Listing
March 2018

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.

Biochem Biophys Res Commun 2018 02 31;496(4):1055-1061. Epub 2018 Jan 31.

Department of Neurology and Neurological Science, Tokyo Medical and Dental University Graduate School of Medical and Dental Sciences, 1-5-45 Yushima Bunkyo-ku, Tokyo 113-8510, Japan.

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http://dx.doi.org/10.1016/j.bbrc.2018.01.119DOI Listing
February 2018

Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation.

Prion 2018 01 31;12(1):54-62. Epub 2018 Jan 31.

a Department of Neuropathology , Institute for Medical Science of Aging, Aichi Medical University , Nagakute , Aichi , Japan.

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http://dx.doi.org/10.1080/19336896.2017.1414130DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5871029PMC
January 2018

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 2017 Dec 13;37(6):575-581. Epub 2017 Jul 13.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12399DOI Listing
December 2017

MM1-type sporadic Creutzfeldt-Jakob disease with 1-month total disease duration and early pathologic indicators.

Neuropathology 2017 Oct 12;37(5):420-425. Epub 2017 Apr 12.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12379DOI Listing
October 2017

An autopsied case of MV2K + C-type sporadic Creutzfeldt-Jakob disease presenting with widespread cerebral cortical involvement and Kuru plaques.

Neuropathology 2017 Jun 7;37(3):241-248. Epub 2016 Nov 7.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12350DOI Listing
June 2017

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 2017 Feb 20;37(1):78-85. Epub 2016 Jul 20.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1111/neup.12327DOI Listing
February 2017

Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy.

Acta Neuropathol 2016 08 17;132(2):313-5. Epub 2016 Jun 17.

Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, 13-1 Takara-machi, Kanazawa, 920-8640, Japan.

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http://dx.doi.org/10.1007/s00401-016-1588-3DOI Listing
August 2016

Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.

Neuropathology 2016 Jun 15;36(3):305-10. Epub 2015 Dec 15.

Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1111/neup.12270DOI Listing
June 2016

Distinctive properties of plaque-type dura mater graft-associated Creutzfeldt-Jakob disease in cell-protein misfolding cyclic amplification.

Lab Invest 2016 05 15;96(5):581-7. Epub 2016 Feb 15.

Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1038/labinvest.2016.27DOI Listing
May 2016

Sporadic Creutzfeldt-Jakob Disease MM1+2C and MM1 are Identical in Transmission Properties.

Brain Pathol 2016 Jan 4;26(1):95-101. Epub 2015 Jun 4.

Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1111/bpa.12264DOI Listing
January 2016

Quantifying prion disease penetrance using large population control cohorts.

Sci Transl Med 2016 Jan;8(322):322ra9

Program in Medical and Population Genetics, Broad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA 02142, USA. Analytical and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA 02114, USA.

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http://dx.doi.org/10.1126/scitranslmed.aad5169DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774245PMC
January 2016

Factors influencing the survival period in Japanese patients with sporadic Creutzfeldt-Jakob disease.

J Neurol Sci 2015 Oct 30;357(1-2):63-8. Epub 2015 Jun 30.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, 1-1 Yazakokarimata, Nagakute 480-1195, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2015.06.065DOI Listing
October 2015

The influence of PRNP polymorphisms on human prion disease susceptibility: an update.

Acta Neuropathol 2015 Aug 29;130(2):159-70. Epub 2015 May 29.

Department of Neurological Science, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, 980-8575, Japan,

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http://link.springer.com/10.1007/s00401-015-1447-7
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http://dx.doi.org/10.1007/s00401-015-1447-7DOI Listing
August 2015

Creutzfeldt-Jakob disease with a codon 210 mutation: first pathological observation in a Japanese patient.

Intern Med 2014 ;53(5):483-7

Department of Neurology, Brain Science Center, Sapporo City General Hospital, Japan.

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http://dx.doi.org/10.2169/internalmedicine.53.0916DOI Listing
May 2015

Creutzfeldt-Jakob disease with homozygous M232R mutation: A case report.

J Neurol Sci 2015 May 19;352(1-2):108-9. Epub 2015 Mar 19.

Department of Neurology, Aomori Prefectural Central Hospital, Aomori, Japan.

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http://dx.doi.org/10.1016/j.jns.2015.03.017DOI Listing
May 2015

Transmission properties of atypical Creutzfeldt-Jakob disease: a clue to disease etiology?

J Virol 2015 Apr 21;89(7):3939-46. Epub 2015 Jan 21.

Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan

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http://dx.doi.org/10.1128/JVI.03183-14DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403436PMC
April 2015

Extensive cortical spongiform changes with cerebellar small amyloid plaques: the clinicopathological case of MV2K+C subtype in Creutzfeldt-Jakob disease.

Neuropathology 2014 Dec 2;34(6):541-6. Epub 2014 Jul 2.

Department of Neurology, National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders, Shizuoka, Japan.

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http://dx.doi.org/10.1111/neup.12133DOI Listing
December 2014

Relation between clinical findings and progression of cerebral cortical pathology in MM1-type sporadic Creutzfeldt-Jakob disease: proposed staging of cerebral cortical pathology.

J Neurol Sci 2014 Jun 13;341(1-2):97-104. Epub 2014 Apr 13.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1016/j.jns.2014.04.011DOI Listing
June 2014

Comparison of the clinical course of Japanese MM1-type sporadic Creutzfeldt-Jakob disease between subacute spongiform encephalopathy and panencephalopathic-type.

Clin Neurol Neurosurg 2014 Jun 1;121:59-63. Epub 2014 Apr 1.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute, Japan.

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http://dx.doi.org/10.1016/j.clineuro.2014.03.024DOI Listing
June 2014

Evaluating prion models based on comprehensive mutation data of mouse PrP.

Structure 2014 Apr 20;22(4):560-71. Epub 2014 Feb 20.

Department of Neurological Science, Tohoku University Graduate School of Medicine Research, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan. Electronic address:

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http://dx.doi.org/10.1016/j.str.2013.12.019DOI Listing
April 2014

Distinct origins of dura mater graft-associated Creutzfeldt-Jakob disease: past and future problems.

Acta Neuropathol Commun 2014 Mar 31;2:32. Epub 2014 Mar 31.

Department of Neurological Science, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.

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http://dx.doi.org/10.1186/2051-5960-2-32DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3976164PMC
March 2014

Critical significance of the region between Helix 1 and 2 for efficient dominant-negative inhibition by conversion-incompetent prion protein.

PLoS Pathog 2013 27;9(6):e1003466. Epub 2013 Jun 27.

Departments of Veterinary Sciences and of Molecular Biology, University of Wyoming, Laramie, Wyoming, United States of America.

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http://dx.doi.org/10.1371/journal.ppat.1003466DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3694865PMC
January 2014

Deciphering the pathogenesis of sporadic Creutzfeldt-Jakob disease with codon 129 M/V and type 2 abnormal prion protein.

Acta Neuropathol Commun 2013 Nov 13;1:74. Epub 2013 Nov 13.

Division of Neurological Science, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.

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http://dx.doi.org/10.1186/2051-5960-1-74DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3833290PMC
November 2013

An autopsied case of Creutzfeldt-Jakob disease with mutation in the prion protein gene codon 232 and type 1+2 prion protein.

Neuropathology 2013 Oct 16;33(5):568-75. Epub 2013 Jan 16.

Department of Neuropathology, Institute for Medical Science of Aging, Aichi Medical University, Nagakute.

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http://doi.wiley.com/10.1111/neup.12013
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http://dx.doi.org/10.1111/neup.12013DOI Listing
October 2013

Insight into the frequent occurrence of dura mater graft-associated Creutzfeldt-Jakob disease in Japan.

J Neurol Neurosurg Psychiatry 2013 Oct 17;84(10):1171-5. Epub 2013 Apr 17.

Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.

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http://dx.doi.org/10.1136/jnnp-2012-304850DOI Listing
October 2013

Characterization of variant Creutzfeldt-Jakob disease prions in prion protein-humanized mice carrying distinct codon 129 genotypes.

J Biol Chem 2013 Jul 21;288(30):21659-66. Epub 2013 Jun 21.

Department of Neurological Science, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.

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http://dx.doi.org/10.1074/jbc.M113.470328DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3724625PMC
July 2013

Quantitative analysis of wet-heat inactivation in bovine spongiform encephalopathy.

Biochem Biophys Res Commun 2013 Mar 30;432(1):86-91. Epub 2013 Jan 30.

Prion Disease Research Center, National Institute of Animal Health, 3-1-5 Kannondai, Tsukuba, Ibaraki 305-0856, Japan.

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http://dx.doi.org/10.1016/j.bbrc.2013.01.081DOI Listing
March 2013

[The infectivity of protein misfolding diseases is reviewed by a prion disease researcher].

Rinsho Shinkeigaku 2011 Nov;51(11):1100

Department of Neurological Science, Tohoku University School of Medicine.

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http://dx.doi.org/10.5692/clinicalneurol.51.1100DOI Listing
November 2011

An autopsy case of MM2-cortical + thalamic-type sporadic Creutzfeldt-Jakob disease.

Neuropathology 2011 Oct 22;31(5):523-30. Epub 2010 Dec 22.

Department of Neurology, National Hospital Organization Higashi Nagoya National Hospital, Nagoya, Japan.

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http://dx.doi.org/10.1111/j.1440-1789.2010.01181.xDOI Listing
October 2011

Slow-progressive ataxia with a methionine-to-arginine point mutation in codon 232 in the prion protein gene (PRNP).

Clin Neurol Neurosurg 2011 Oct 28;113(8):696-8. Epub 2011 May 28.

Department of Neurology, School of Medicine, Keio University, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

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http://dx.doi.org/10.1016/j.clineuro.2011.04.009DOI Listing
October 2011

Deduction of the evaluation limit and termination timing of multi-round protein misfolding cyclic amplification from a titration curve.

Microbiol Immunol 2011 Jul;55(7):502-9

Department of Neurological Science, Tohoku University Graduate School of Medicine, Japan.

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http://dx.doi.org/10.1111/j.1348-0421.2011.00340.xDOI Listing
July 2011

Heparin enhances the cell-protein misfolding cyclic amplification efficiency of variant Creutzfeldt-Jakob disease.

Neurosci Lett 2011 Jul 5;498(2):119-23. Epub 2011 May 5.

Research and Development Division, Benesis Corporation, c/o Division of Neurological Science, Department of Prion Research, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai, Japan.

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http://dx.doi.org/10.1016/j.neulet.2011.04.072DOI Listing
July 2011

Co-occurrence of types 1 and 2 PrP(res) in sporadic Creutzfeldt-Jakob disease MM1.

Am J Pathol 2011 Mar;178(3):1309-15

Division of Neurological Science, Center for Prion Research, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1016/j.ajpath.2010.11.069DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3069892PMC
March 2011

Serial diffusion-weighted MRI and SPECT findings in a Creutzfeldt-Jakob disease patient with V180I mutation.

J Neurol Sci 2011 Feb 20;301(1-2):100-3. Epub 2010 Nov 20.

Department of Neurology, National Hospital Organization Okayama Medical Center, Okayama, Japan.

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http://dx.doi.org/10.1016/j.jns.2010.10.032DOI Listing
February 2011

An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.

Neuropathology 2010 Apr 23;30(2):159-64. Epub 2009 Aug 23.

Department of Neuropsychiatry, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences.

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http://doi.wiley.com/10.1111/j.1440-1789.2009.01048.x
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http://dx.doi.org/10.1111/j.1440-1789.2009.01048.xDOI Listing
April 2010

Experimental verification of a traceback phenomenon in prion infection.

J Virol 2010 Apr 20;84(7):3230-8. Epub 2010 Jan 20.

Division of CJD Science and Technology, Department of Prion Research, Tohoku University Graduate School of Medicine, 2-1 Seiryo-machi, Aoba-ku, Sendai 980-8575, Japan.

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http://dx.doi.org/10.1128/JVI.02387-09DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838106PMC
April 2010

Age-dependent increase in lysosome-associated membrane protein 1 and early-onset behavioral deficits in APPSL transgenic mouse model of Alzheimer's disease.

Neurosci Lett 2010 Jan 16;469(2):273-7. Epub 2009 Dec 16.

Graduate School of Biosphere Science, Hiroshima University, 1-7-1 Kagamiyama, Higashi-hiroshima 739-8521, Japan.

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http://dx.doi.org/10.1016/j.neulet.2009.12.015DOI Listing
January 2010

Amino acid conditions near the GPI anchor attachment site of prion protein for the conversion and the GPI anchoring.

Biochem Biophys Res Commun 2010 Jan 29;391(4):1681-6. Epub 2009 Dec 29.

Division of CJD Science and Technology, Department of Prion Research, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.

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http://dx.doi.org/10.1016/j.bbrc.2009.12.128DOI Listing
January 2010

[History of 50 years of prion disease research].

Rinsho Shinkeigaku 2009 Nov;49(11):936-8

Department of Prion Protein Research, Center for Translational and Advanced Animal Research on Human Diseases, Tohoku University Graduate School of Medicine.

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http://dx.doi.org/10.5692/clinicalneurol.49.936DOI Listing
November 2009

[Prion disease surveillance in Japan: analysis of 1,241 patients].

Rinsho Shinkeigaku 2009 Nov;49(11):939-42

Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science.

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http://dx.doi.org/10.5692/clinicalneurol.49.939DOI Listing
November 2009

Dura mater graft-associated Creutzfeldt-Jakob disease in Japan: clinicopathological and molecular characterization of the two distinct subtypes.

Neuropathology 2009 Oct 29;29(5):609-18. Epub 2009 Jul 29.

Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.

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http://dx.doi.org/10.1111/j.1440-1789.2008.00987.xDOI Listing
October 2009

A traceback phenomenon can reveal the origin of prion infection.

Neuropathology 2009 Oct 29;29(5):619-24. Epub 2009 Jul 29.

Division of CJD Science and Technology, Department of Prion Research, Tohoku University Graduate School of Medicine, Miyagi, Japan.

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http://dx.doi.org/10.1111/j.1440-1789.2008.00973.xDOI Listing
October 2009

The risk of iatrogenic Creutzfeldt-Jakob disease through medical and surgical procedures.

Neuropathology 2009 Oct 29;29(5):625-31. Epub 2009 Jul 29.

Department of Neurology and Neurobiology of Aging, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.

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http://dx.doi.org/10.1111/j.1440-1789.2009.01023.xDOI Listing
October 2009

Unique clinicopathological features and PrP profiles in the first autopsied case of dura mater graft-associated Creutzfeldt-Jakob disease with codon 219 lysine allele observed in Japanese population.

J Neurol Sci 2009 Oct 8;285(1-2):265-7. Epub 2009 Aug 8.

Second Department of Internal Medicine (Neurology), Faculty of Medical Sciences, University of Fukui, 23-3 Shimoaiduki, Matsuoka, Eiheiji-cho, Yoshida-gun, Fukui 910-1193, Japan.

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http://linkinghub.elsevier.com/retrieve/pii/S0022510X0900741
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http://dx.doi.org/10.1016/j.jns.2009.07.019DOI Listing
October 2009

A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.

Clin Neurol Neurosurg 2009 Sep 13;111(7):606-9. Epub 2009 May 13.

Department of Neurology, Oyamada Memorial Spa Hospital, 5538-1 Yamada-cho, Yokkaichi 512-1111, Japan.

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http://linkinghub.elsevier.com/retrieve/pii/S030384670900080
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http://dx.doi.org/10.1016/j.clineuro.2009.03.008DOI Listing
September 2009

Heterozygous inhibition in prion infection: the stone fence model.

Prion 2009 Jan-Mar;3(1):27-30. Epub 2009 Jan 23.

Division of CJD Science and Technology, Department of Prion Research, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2676740PMC
http://dx.doi.org/10.4161/pri.3.1.8514DOI Listing
June 2009

The number of octapeptide repeat affects the expression and conversion of prion protein.

Biochem Biophys Res Commun 2009 May 24;382(4):715-9. Epub 2009 Mar 24.

Division of CJD Science and Technology, Department of Prion Research, Tohoku University Graduate School of Medicine, Sendai, Japan.

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http://dx.doi.org/10.1016/j.bbrc.2009.03.093DOI Listing
May 2009