Similar articles for PMID: 8570627

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1976	1
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1

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

Ghetti B, Piccardo P, Spillantini MG, Ichimiya Y, Porro M, Perini F, Kitamoto T, Tateishi J, Seiler C, Frangione B, Bugiani O, Giaccone G, Prelli F, Goedert M, Dlouhy SR, Tagliavini F. Ghetti B, et al. Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):744-8. doi: 10.1073/pnas.93.2.744. Proc Natl Acad Sci U S A. 1996. PMID: 8570627 Free PMC article.

2

Structure of Tau filaments in Prion protein amyloidoses.

Hallinan GI, Hoq MR, Ghosh M, Vago FS, Fernandez A, Garringer HJ, Vidal R, Jiang W, Ghetti B. Hallinan GI, et al. Acta Neuropathol. 2021 Aug;142(2):227-241. doi: 10.1007/s00401-021-02336-w. Epub 2021 Jun 14. Acta Neuropathol. 2021. PMID: 34128081 Free PMC article.

3

Prion-associated cerebral amyloid angiopathy is not exacerbated by human phosphorylated tau aggregates in scrapie-infected mice expressing anchorless prion protein.

Race B, Williams K, Striebel JF, Chesebro B. Race B, et al. Neurobiol Dis. 2020 Oct;144:105057. doi: 10.1016/j.nbd.2020.105057. Epub 2020 Aug 21. Neurobiol Dis. 2020. PMID: 32829029 Free article.

4

Vascular disease and cerebral amyloid deposition.

[No authors listed] [No authors listed] Neurology. 2018 Aug 14;91(7):333. doi: 10.1212/WNL.0000000000005703. Neurology. 2018. PMID: 30104233 No abstract available.

5

Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker.

Ghetti B, Piccardo P, Zanusso G. Ghetti B, et al. Handb Clin Neurol. 2018;153:243-269. doi: 10.1016/B978-0-444-63945-5.00014-3. Handb Clin Neurol. 2018. PMID: 29887140

6

Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study.

Cali I, Cohen ML, Haik S, Parchi P, Giaccone G, Collins SJ, Kofskey D, Wang H, McLean CA, Brandel JP, Privat N, Sazdovitch V, Duyckaerts C, Kitamoto T, Belay ED, Maddox RA, Tagliavini F, Pocchiari M, Leschek E, Appleby BS, Safar JG, Schonberger LB, Gambetti P. Cali I, et al. Acta Neuropathol Commun. 2018 Jan 8;6(1):5. doi: 10.1186/s40478-017-0503-z. Acta Neuropathol Commun. 2018. PMID: 29310723 Free PMC article.

7

C-Terminal-Deleted Prion Protein Fragment Is a Major Accumulated Component of Systemic PrP Deposits in Hereditary Prion Disease With a 2-Bp (CT) Deletion in PRNP Codon 178.

Honda H, Matsuzono K, Fushimi S, Sato K, Suzuki SO, Abe K, Iwaki T. Honda H, et al. J Neuropathol Exp Neurol. 2016 Nov 1;75(11):1008-1019. doi: 10.1093/jnen/nlw077. J Neuropathol Exp Neurol. 2016. PMID: 27634965

8

'PrP systemic deposition disease': clinical and pathological characteristics of novel familial prion disease with 2-bp deletion in codon 178.

Matsuzono K, Honda H, Sato K, Morihara R, Deguchi K, Hishikawa N, Yamashita T, Kono S, Ohta Y, Iwaki T, Abe K. Matsuzono K, et al. Eur J Neurol. 2016 Jan;23(1):196-200. doi: 10.1111/ene.12905. Eur J Neurol. 2016. PMID: 26768678 Free article.

9

[Cerebral amyloid angiopathy].

Sakai K, Yamada M. Sakai K, et al. Brain Nerve. 2014 Jul;66(7):827-35. Brain Nerve. 2014. PMID: 24998827 Japanese.

10

Molecular cloning and sequence analysis of prion protein gene in Xiji donkey in China.

Zhang Z, Wang R, Xu L, Yuan F, Zhou X, Yang L, Yin X, Xu B, Zhao D. Zhang Z, et al. Gene. 2013 Oct 25;529(2):345-50. doi: 10.1016/j.gene.2013.08.019. Epub 2013 Aug 15. Gene. 2013. PMID: 23954254

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