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Items: 1 to 20 of 120

1.

Spreading brain lesions in a familial Creutzfeldt-Jakob disease with V180I mutation over 4 years.

Deguchi K, Takamiya M, Deguchi S, Morimoto N, Kurata T, Ikeda Y, Abe K.

BMC Neurol. 2012 Nov 24;12:144. doi: 10.1186/1471-2377-12-144.

2.

Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.

Amano Y, Kimura N, Hanaoka T, Aso Y, Hirano T, Murai H, Satoh K, Matsubara E.

Prion. 2015;9(1):29-33. doi: 10.1080/19336896.2015.1017703.

3.

[Clinicopathological characteristics of Creutzfeldt-Jakob disease with a PrP V180I mutation and M129V polymorphism on different alleles].

Iwaski Y, Sone M, Kato T, Yoshida E, Indo T, Yoshida M, Hashizume Y, Yamada M.

Rinsho Shinkeigaku. 1999 Aug;39(8):800-6. Review. Japanese.

PMID:
10586622
4.

Lateralized and focal clinical, EEG, and FLAIR MRI abnormalities in Creutzfeldt-Jakob disease.

Cambier DM, Kantarci K, Worrell GA, Westmoreland BF, Aksamit AJ.

Clin Neurophysiol. 2003 Sep;114(9):1724-8.

PMID:
12948802
5.

Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.

Tsuboi Y, Baba Y, Doh-ura K, Imamura A, Fujioka S, Yamada T.

J Neurol Sci. 2005 May 15;232(1-2):45-9.

PMID:
15850581
6.

[A case of MM1+2 Creutzfeldt-Jakob disease with a longitudinal study of EEG and MRI].

Katsube M, Shiota Y, Harada T, Shibata H, Nagai A.

Rinsho Byori. 2013 Nov;61(11):995-1000. Japanese.

PMID:
24450104
7.

Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.

Shi Q, Shen XJ, Zhou W, Xiao K, Zhang XM, Zhang BY, Dong XP.

Prion. 2014;8(6):411-4. doi: 10.4161/19336896.2014.967040.

8.

[A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings].

Kobayashi S, Ohuchi T, Maki T.

Rinsho Shinkeigaku. 1997 Aug;37(8):671-4. Japanese.

PMID:
9404141
9.

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

Kono S, Manabe Y, Fujii D, Sakai Y, Narai H, Omori N, Kitamoto T, Abe K.

J Neurol Sci. 2011 Feb 15;301(1-2):100-3. doi: 10.1016/j.jns.2010.10.032. Epub 2010 Nov 20.

PMID:
21094959
10.

[Serial magnetic resonance images of a Creutzfeldt-Jakob disease patient with V180I mutation obtained over 10 years].

Shimizu H, Shiga Y, Matsumoto A, Hisanaga K.

Rinsho Shinkeigaku. 2013;53(3):235-8. Japanese.

PMID:
23524605
11.

[A case of codon 232 mutation-induced Creutzfeldt-Jakob disease visualized by the MRI-FLAIR images with atypical clinical symptoms].

Saito T, Isozumi K, Komatsumoto S, Nara M, Suzuki K, Dohura K.

Rinsho Shinkeigaku. 2000 Jan;40(1):51-4. Japanese.

PMID:
10825802
12.

Creutzfeldt Jakob disease.

Haider E, Wali W, Raja S, Tariq M.

J Coll Physicians Surg Pak. 2013 Apr;23(4):295-7. doi: 04.2013/JCPSP.295297.

PMID:
23552545
13.

Familial Creutzfeldt-Jakob disease with a mutation at codon 180 presenting with an atypical phenotype.

Yeo MJ, Lee SH, Lee SY, Jeon YC, Park SJ, Cho HJ, Choi KC, Kim YS, Kim SH.

J Clin Neurosci. 2013 Jan;20(1):180-2. doi: 10.1016/j.jocn.2012.01.044. Epub 2012 Sep 19.

PMID:
22999564
14.

[A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180].

Tanaka T, Kinoshita I, Saitoh Y, Satoh K, Nishiura Y, Shirabe S, Kitamoto T.

No To Shinkei. 2004 Dec;56(12):1025-8. Review. Japanese.

PMID:
15729879
15.

Correlation between periodic sharp wave complexes and diffusion-weighted magnetic resonance images in early stage of Creutzfeldt-Jakob disease: a report of two cases.

Mizobuchi M, Tanaka C, Sako K, Nihira A, Abe T, Shirasawa A.

Seizure. 2008 Dec;17(8):717-22. doi: 10.1016/j.seizure.2008.05.012. Epub 2008 Jul 3.

16.

The EEG in E200K familial CJD: relation to MRI patterns.

Appel SA, Chapman J, Prohovnik I, Hoffman C, Cohen OS, Blatt I.

J Neurol. 2012 Mar;259(3):491-6. doi: 10.1007/s00415-011-6208-5. Epub 2011 Aug 12.

PMID:
21833705
17.

Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images.

Mutsukura K, Satoh K, Shirabe S, Tomita I, Fukutome T, Morikawa M, Iseki M, Sasaki K, Shiaga Y, Kitamoto T, Eguchi K.

Dement Geriatr Cogn Disord. 2009;28(6):550-7. doi: 10.1159/000254842. Epub 2009 Dec 30.

18.

[Diffusion images on brain MRI in Creutzfeldt-Jakob disease].

Nagaoka U, Kurita K, Hosoya T, Kitamoto T, Kato T.

Rinsho Shinkeigaku. 1999 Apr;39(4):468-70. Japanese.

PMID:
10391976
19.

Rare V203I mutation in the PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease.

Shi Q, Chen C, Wang XJ, Zhou W, Wang JC, Zhang BY, Gao C, Gao C, Han J, Dong XP.

Prion. 2013 May-Jun;7(3):259-62. doi: 10.4161/pri.24674.

20.

Diffusion-weighted magnetic resonance imaging in diagnosis of Creutzfeldt-Jakob disease.

Lou X, Ma L, An NY, Cai YQ, Liang Y, Guo XG.

Chin Med J (Engl). 2006 Aug 5;119(15):1242-7.

PMID:
16919182

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