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Items: 1 to 20 of 86

1.

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

Kobayashi A, Matsuura Y, Mohri S, Kitamoto T.

Acta Neuropathol Commun. 2014 Mar 31;2:32. doi: 10.1186/2051-5960-2-32. Review.

2.

A traceback phenomenon can reveal the origin of prion infection.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29.

PMID:
19659941
3.

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

Yamada M, Noguchi-Shinohara M, Hamaguchi T, Nozaki I, Kitamoto T, Sato T, Nakamura Y, Mizusawa H.

Neuropathology. 2009 Oct;29(5):609-18. doi: 10.1111/j.1440-1789.2008.00987.x. Epub 2009 Jul 29.

PMID:
19659940
4.

Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease.

Noguchi-Shinohara M, Hamaguchi T, Kitamoto T, Sato T, Nakamura Y, Mizusawa H, Yamada M.

Neurology. 2007 Jul 24;69(4):360-7.

PMID:
17646628
5.

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

Takeuchi A, Kobayashi A, Parchi P, Yamada M, Morita M, Uno S, Kitamoto T.

Lab Invest. 2016 May;96(5):581-7. doi: 10.1038/labinvest.2016.27. Epub 2016 Feb 15.

6.

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

Kobayashi A, Matsuura Y, Iwaki T, Iwasaki Y, Yoshida M, Takahashi H, Murayama S, Takao M, Kato S, Yamada M, Mohri S, Kitamoto T.

Brain Pathol. 2016 Jan;26(1):95-101. doi: 10.1111/bpa.12264. Epub 2015 Jun 4.

PMID:
25851836
7.

Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain.

Kobayashi A, Asano M, Mohri S, Kitamoto T.

J Biol Chem. 2007 Oct 12;282(41):30022-8. Epub 2007 Aug 20.

8.

Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases.

Satoh K, Muramoto T, Tanaka T, Kitamoto N, Ironside JW, Nagashima K, Yamada M, Sato T, Mohri S, Kitamoto T.

J Gen Virol. 2003 Oct;84(Pt 10):2885-93.

PMID:
13679624
9.

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

Hamaguchi T, Sakai K, Noguchi-Shinohara M, Nozaki I, Takumi I, Sanjo N, Sadakane A, Nakamura Y, Kitamoto T, Saito N, Mizusawa H, Yamada M.

J Neurol Neurosurg Psychiatry. 2013 Oct;84(10):1171-5. doi: 10.1136/jnnp-2012-304850. Epub 2013 Apr 17.

PMID:
23595947
10.

[Clinical manifestations and epidemiology of prion diseases in Japan].

Hamaguchi T.

Rinsho Shinkeigaku. 2013;23(11):1246-8. Japanese.

PMID:
24291945
11.

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

Kobayashi A, Parchi P, Yamada M, Brown P, Saverioni D, Matsuura Y, Takeuchi A, Mohri S, Kitamoto T.

J Virol. 2015 Apr;89(7):3939-46. doi: 10.1128/JVI.03183-14. Epub 2015 Jan 21.

12.

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.

Ikawa M, Yoneda M, Matsunaga A, Nakagawa H, Kazama-Suzuki A, Miyashita N, Naiki H, Kitamoto T, Kuriyama M.

J Neurol Sci. 2009 Oct 15;285(1-2):265-7. doi: 10.1016/j.jns.2009.07.019. Epub 2009 Aug 8.

PMID:
19666177
13.

Increased asymmetric pulvinar magnetic resonance imaging signals in Creutzfeldt-Jakob disease with florid plaques following a cadaveric dura mater graft.

Wakisaka Y, Santa N, Doh-ura K, Kitamoto T, Ibayashi S, Iida M, Iwaki T.

Neuropathology. 2006 Feb;26(1):82-8.

PMID:
16521484
14.

Clinicopathologic characteristics of five autopsied cases of dura mater-associated Creutzfeldt-Jakob disease.

Iwasaki Y, Mimuro M, Yoshida M, Hashizume Y, Kitamoto T, Sobue G.

Neuropathology. 2008 Feb;28(1):51-61. doi: 10.1111/j.1440-1789.2007.00847.x.

PMID:
18181835
15.

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

Yamada M, Nozaki I, Hamaguchi T, Noguchi-Shinohara M, Kitamoto T, Nakamura Y, Sato T, Mizusawa H.

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

PMID:
20030254
16.

[Infectious prion disease: CJD with dura mater transplantation].

Sato T.

Rinsho Shinkeigaku. 2003 Nov;43(11):870-2. Review. Japanese.

PMID:
15152489
17.

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

Kobayashi A, Mizukoshi K, Iwasaki Y, Miyata H, Yoshida Y, Kitamoto T.

Am J Pathol. 2011 Mar;178(3):1309-15. doi: 10.1016/j.ajpath.2010.11.069.

18.

Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions.

Taguchi Y, Mohri S, Ironside JW, Muramoto T, Kitamoto T.

Am J Pathol. 2003 Dec;163(6):2585-93.

19.

Creutzfeldt-Jakob disease with florid plaques after cadaveric dura mater graft.

Mochizuki Y, Mizutani T, Tajiri N, Oinuma T, Nemoto N, Kakimi S, Kitamoto T.

Neuropathology. 2003 Jun;23(2):136-40.

PMID:
12777102
20.

A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report.

Rodríguez-Martínez AB, Garrido JM, Zarranz JJ, Arteagoitia JM, de Pancorbo MM, Atarés B, Bilbao MJ, Ferrer I, Juste RA.

BMC Neurol. 2010 Oct 25;10:99. doi: 10.1186/1471-2377-10-99.

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