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Items: 1 to 20 of 90

1.

Panencephalopathic-type sporadic Creutzfeldt-Jakob disease with circumscribed spongy foci.

Iwasaki Y, Tatsumi S, Mimuro M, Mori K, Ito M, Kitamoto T, Yoshida M.

Clin Neuropathol. 2014 Mar-Apr;33(2):160-4. doi: 10.5414/NP300684. No abstract available.

PMID:
24131752
2.

Creutzfeldt-Jakob disease. Report of a case of the panencephalopathic type and experiences of a teaching hospital in Taiwan.

Su MS, Wang SJ, Chiang H, Wang JS, Tan YA, Fuh JL, Liu HC.

Eur Neurol. 1993;33(3):241-3.

PMID:
8467846
3.
4.

Creutzfeldt-Jakob disease: analysis of the MRI signal.

Urbach H.

Neuroreport. 2000 Nov 27;11(17):L5-6. No abstract available.

PMID:
11117520
5.

Cortical restricted diffusion as the predominant MRI finding in sporadic Creutzfeldt-Jakob disease.

Talbott SD, Plato BM, Sattenberg RJ, Parker J, Heidenreich JO.

Acta Radiol. 2011 Apr 1;52(3):336-9. doi: 10.1258/ar.2010.100355. Epub 2011 Mar 3.

PMID:
21498372
6.

[T2-weighted MRI and pathological findings in the cerebral hemisphere of panencephalitic Creutzfeldt-Jakob disease].

Konagaya M, Sakai M, Asakura K, Matsuoka Y, Hashizume Y.

No To Shinkei. 2001 Apr;53(4):398-9. Japanese. No abstract available.

PMID:
11360483
7.

Amyotrophic form of Creutzfeldt-Jakob disease with rapid course in 82-year-old man.

Nowacki P, Kulczycki J, Narolewska A, Grzelec H.

Folia Neuropathol. 2000;38(4):161-3. Review.

PMID:
11693718
8.

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.

Ishida C, Kakishima A, Okino S, Furukawa Y, Kano M, Oda Y, Nakanishi I, Makifuchi T, Kitamoto T, Yamada M.

Neurology. 2003 Feb 11;60(3):514-7.

PMID:
12578942
9.

Familial Creutzfeldt-Jakob disease: three autopsy cases of the panencephalopathic type.

Seno H, Ishino H, Inagaki T, Yamamori C, Iijima M, Tanaka S, Kobayashi S, Shimizu Y, Torii I, Harada T.

Clin Neuropathol. 1994 Jul-Aug;13(4):185-91.

PMID:
7955663
10.

White matter lesions in panencephalopathic type of Creutzfeldt-Jakob disease: MR imaging and pathologic correlations.

Matsusue E, Kinoshita T, Sugihara S, Fujii S, Ogawa T, Ohama E.

AJNR Am J Neuroradiol. 2004 Jun-Jul;25(6):910-8.

11.

Diffusion-weighted MRI in sporadic Creutzfeldt-Jakob disease.

Demaerel P, Heiner L, Robberecht W, Sciot R, Wilms G.

Neurology. 1999 Jan 1;52(1):205-8.

PMID:
9921880
12.

An atypical form of sporadic panencephalopathic Creutzfeldt-Jakob disease in Japan.

Yamamoto S, Furukawa H, Kitamoto T, Takamaru Y, Morita N, Yasuda M, Okada Y, Sawa H, Nagashima K.

Neuropathol Appl Neurobiol. 2003 Feb;29(1):77-80. No abstract available.

PMID:
12581342
13.

Sporadic Creutzfeldt-Jakob disease: magnetic resonance imaging and clinical findings.

Iwasaki Y, Igarashi O, Ichikawa Y, Ikeda K.

Neurology. 2005 Apr 12;64(7):1318; author reply 1318. No abstract available.

PMID:
15824383
14.

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

Hama T, Iwasaki Y, Niwa H, Yoshida M, Hashizume Y, Kitamoto T, Murakami N, Sobue G.

Neuropathology. 2009 Dec;29(6):727-34. doi: 10.1111/j.1440-1789.2009.01016.x. Epub 2009 Apr 28.

PMID:
19422533
15.

FLAIR MRI in sporadic Creutzfeldt-Jakob disease.

Vrancken AF, Frijns CJ, Ramos LM.

Neurology. 2000 Jul 12;55(1):147-8. No abstract available.

PMID:
10891930
16.

Asymmetric involvement in sporadic creutzfeldt-jakob disease: clinical, brain imaging, and electroencephalographic studies.

Wu HM, Lu CS, Huang CC, Lyu RK, Chen RS, Wu YR, Chen YC, Lai SC, Hung J, Tsai YT, Toh CH, Kuo HC.

Eur Neurol. 2010;64(2):74-9. doi: 10.1159/000315148. Epub 2010 Jul 3.

PMID:
20606451
17.

Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity at codon 129 and prion protein type 2.

Samman I, Schulz-Schaeffer WJ, Wöhrle JC, Sommer A, Kretzschmar HA, Hennerici M.

J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):678-81.

18.

Brain biopsy and patients with atypical presentations of sporadic Creutzfeldt-Jakob disease.

Whittle IR, Will RG, Ironside JW.

J Neurol Neurosurg Psychiatry. 1997 Oct;63(4):547-8. No abstract available.

19.

[Panencephalopathy of the Creutzfeldt-Jakob disease type].

Gertz HJ, Stoltenburg G, Cruz-Sanchez F, Lafuente J, Schopol R.

Nervenarzt. 1988 Feb;59(2):110-2. German.

PMID:
3283576
20.

[Panencephalopathic type of Creutzfeldt-Jakob disease and special reference to its pyramidal tract degeneration].

Riku S, Okamoto T, Hashizume Y, Koike Y, Sobue I.

Rinsho Shinkeigaku. 1983 Feb;23(2):147-51. Japanese. No abstract available.

PMID:
6345044

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