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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1968 1
1980 1
1991 1
1992 2
1993 1
1996 4
1997 6
1998 2
1999 5
2000 1
2001 5
2002 6
2003 6
2004 9
2005 6
2006 11
2007 7
2008 8
2009 16
2010 11
2011 9
2012 9
2013 7
2014 13
2015 10
2016 8
2017 6
2018 4
2019 2
2020 7
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Similar Articles for PMID: 18635614

165 results
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Page 1
MR imaging of familial Creutzfeldt-Jakob disease: a blinded and controlled study.
Fulbright RK, Hoffmann C, Lee H, Pozamantir A, Chapman J, Prohovnik I. Fulbright RK, et al. AJNR Am J Neuroradiol. 2008 Oct;29(9):1638-43. doi: 10.3174/ajnr.A1217. Epub 2008 Jul 17. AJNR Am J Neuroradiol. 2008. PMID: 18635614 Free article.
Creutzfeldt-Jakob disease: comparative analysis of MR imaging sequences.
Kallenberg K, Schulz-Schaeffer WJ, Jastrow U, Poser S, Meissner B, Tschampa HJ, Zerr I, Knauth M. Kallenberg K, et al. AJNR Am J Neuroradiol. 2006 Aug;27(7):1459-62. AJNR Am J Neuroradiol. 2006. PMID: 16908558 Free article.
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. Tsuboi Y, et al. J Neurol Sci. 2005 May 15;232(1-2):45-9. doi: 10.1016/j.jns.2005.01.006. J Neurol Sci. 2005. PMID: 15850581
Isolated cortical signal increase on MR imaging as a frequent lesion pattern in sporadic Creutzfeldt-Jakob disease.
Meissner B, Kallenberg K, Sanchez-Juan P, Krasnianski A, Heinemann U, Varges D, Knauth M, Zerr I. Meissner B, et al. AJNR Am J Neuroradiol. 2008 Sep;29(8):1519-24. doi: 10.3174/ajnr.A1122. Epub 2008 Jul 3. AJNR Am J Neuroradiol. 2008. PMID: 18599580 Free article.
Magnetic resonance imaging in E200K and V210I mutations of the prion protein gene.
Breithaupt M, Romero C, Kallenberg K, Begue C, Sanchez-Juan P, Eigenbrod S, Kretzschmar H, Schelzke G, Meichtry E, Taratuto A, Zerr I. Breithaupt M, et al. Alzheimer Dis Assoc Disord. 2013 Jan-Mar;27(1):87-90. doi: 10.1097/WAD.0b013e31824d578a. Alzheimer Dis Assoc Disord. 2013. PMID: 22407223
The imaging appearance of Creutzfeldt-Jakob disease caused by the E200K mutation.
Fulbright RK, Kingsley PB, Guo X, Hoffmann C, Kahana E, Chapman JC, Prohovnik I. Fulbright RK, et al. Magn Reson Imaging. 2006 Nov;24(9):1121-9. doi: 10.1016/j.mri.2006.07.001. Epub 2006 Sep 7. Magn Reson Imaging. 2006. PMID: 17071334
Thalamic involvement in sporadic Creutzfeldt-Jakob disease: a diffusion-weighted MR imaging study.
Tschampa HJ, Mürtz P, Flacke S, Paus S, Schild HH, Urbach H. Tschampa HJ, et al. AJNR Am J Neuroradiol. 2003 May;24(5):908-15. AJNR Am J Neuroradiol. 2003. PMID: 12748093 Free article.
Familial Creutzfeldt-Jakob disease with the E200K mutation: longitudinal neuroimaging from asymptomatic to symptomatic CJD.
Cohen OS, Chapman J, Korczyn AD, Nitsan Z, Appel S, Hoffmann C, Rosenmann H, Kahana E, Lee H. Cohen OS, et al. J Neurol. 2015 Mar;262(3):604-13. doi: 10.1007/s00415-014-7615-1. Epub 2014 Dec 19. J Neurol. 2015. PMID: 25522698
Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.
Young GS, Geschwind MD, Fischbein NJ, Martindale JL, Henry RG, Liu S, Lu Y, Wong S, Liu H, Miller BL, Dillon WP. Young GS, et al. AJNR Am J Neuroradiol. 2005 Jun-Jul;26(6):1551-62. AJNR Am J Neuroradiol. 2005. PMID: 15956529 Free article.
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
Zerr I, Kallenberg K, Summers DM, Romero C, Taratuto A, Heinemann U, Breithaupt M, Varges D, Meissner B, Ladogana A, Schuur M, Haik S, Collins SJ, Jansen GH, Stokin GB, Pimentel J, Hewer E, Collie D, Smith P, Roberts H, Brandel JP, van Duijn C, Pocchiari M, Begue C, Cras P, Will RG, Sanchez-Juan P. Zerr I, et al. Brain. 2009 Oct;132(Pt 10):2659-68. doi: 10.1093/brain/awp191. Epub 2009 Sep 22. Brain. 2009. PMID: 19773352 Free PMC article.
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