Similar articles for PMID: 16113366

Year	Number of Results
1948	1
1961	1
1991	1
1992	1
1993	1
1995	1
1996	2
1999	2
2000	6
2001	1
2002	9
2003	6
2004	11
2005	8
2006	4
2007	4
2008	6
2009	8
2010	7
2011	4
2012	1
2013	3
2014	7
2015	4
2016	6
2017	2
2018	9
2019	3
2020	4
2021	7
2022	5
2023	2
2024	0

1

Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease.

Head MW, Peden AH, Yull HM, Ritchie DL, Bonshek RE, Tullo AB, Ironside JW. Head MW, et al. Br J Ophthalmol. 2005 Sep;89(9):1131-3. doi: 10.1136/bjo.2004.063495. Br J Ophthalmol. 2005. PMID: 16113366 Free PMC article.

2

Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.

Faucheux BA, Morain E, Diouron V, Brandel JP, Salomon D, Sazdovitch V, Privat N, Laplanche JL, Hauw JJ, Haïk S. Faucheux BA, et al. Neuropathol Appl Neurobiol. 2011 Aug;37(5):500-12. doi: 10.1111/j.1365-2990.2011.01179.x. Neuropathol Appl Neurobiol. 2011. PMID: 21450052

3

Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease.

Schoch G, Seeger H, Bogousslavsky J, Tolnay M, Janzer RC, Aguzzi A, Glatzel M. Schoch G, et al. PLoS Med. 2006 Feb;3(2):e14. doi: 10.1371/journal.pmed.0030014. Epub 2005 Dec 20. PLoS Med. 2006. PMID: 16354106 Free PMC article.

4

Extraneural pathologic prion protein in sporadic Creutzfeldt-Jakob disease.

Glatzel M, Abela E, Maissen M, Aguzzi A. Glatzel M, et al. N Engl J Med. 2003 Nov 6;349(19):1812-20. doi: 10.1056/NEJMoa030351. N Engl J Med. 2003. PMID: 14602879 Free article.

5

Pathologic prion protein spreading in the peripheral nervous system of a patient with sporadic Creutzfeldt-Jakob disease.

Favereaux A, Quadrio I, Vital C, Perret-Liaudet A, Anne O, Laplanche JL, Petry KG, Vital A. Favereaux A, et al. Arch Neurol. 2004 May;61(5):747-50. doi: 10.1001/archneur.61.5.747. Arch Neurol. 2004. PMID: 15148153

6

Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients.

Orrù CD, Soldau K, Cordano C, Llibre-Guerra J, Green AJ, Sanchez H, Groveman BR, Edland SD, Safar JG, Lin JH, Caughey B, Geschwind MD, Sigurdson CJ. Orrù CD, et al. mBio. 2018 Nov 20;9(6):e02095-18. doi: 10.1128/mBio.02095-18. mBio. 2018. PMID: 30459197 Free PMC article.

7

Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease.

Zanusso G, Ferrari S, Cardone F, Zampieri P, Gelati M, Fiorini M, Farinazzo A, Gardiman M, Cavallaro T, Bentivoglio M, Righetti PG, Pocchiari M, Rizzuto N, Monaco S. Zanusso G, et al. N Engl J Med. 2003 Feb 20;348(8):711-9. doi: 10.1056/NEJMoa022043. N Engl J Med. 2003. PMID: 12594315 Free article.

8

Association between deposition of beta-amyloid and pathological prion protein in sporadic Creutzfeldt-Jakob disease.

Debatin L, Streffer J, Geissen M, Matschke J, Aguzzi A, Glatzel M. Debatin L, et al. Neurodegener Dis. 2008;5(6):347-54. doi: 10.1159/000121389. Epub 2008 Mar 18. Neurodegener Dis. 2008. PMID: 18349519 Free article.

9

Advances in the detection of prion protein in peripheral tissues of variant Creutzfeldt-Jakob disease patients using paraffin-embedded tissue blotting.

Ritchie DL, Head MW, Ironside JW. Ritchie DL, et al. Neuropathol Appl Neurobiol. 2004 Aug;30(4):360-8. doi: 10.1111/j.1365-2990.2003.00544.x. Neuropathol Appl Neurobiol. 2004. PMID: 15305981

10

Disease-associated prion protein in vessel walls.

Koperek O, Kovács GG, Ritchie D, Ironside JW, Budka H, Wick G. Koperek O, et al. Am J Pathol. 2002 Dec;161(6):1979-84. doi: 10.1016/S0002-9440(10)64474-4. Am J Pathol. 2002. PMID: 12466112 Free PMC article.

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