Similar articles for PMID: 23538413

Year	Number of Results
1992	1
1993	7
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1998	4
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2012	4
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1

Imaging of the 6-OPRI mutation prion disease: an entity distinct from typical Creutzfeldt-Jakob disease?

Degnan AJ, Levy LM. Degnan AJ, et al. AJNR Am J Neuroradiol. 2013 Sep;34(9):1731-2. doi: 10.3174/ajnr.A3490. Epub 2013 Mar 28. AJNR Am J Neuroradiol. 2013. PMID: 23538413 Free PMC article. No abstract available.

2

Multiparameter MR imaging in the 6-OPRI variant of inherited prion disease.

De Vita E, Ridgway GR, Scahill RI, Caine D, Rudge P, Yousry TA, Mead S, Collinge J, Jäger HR, Thornton JS, Hyare H. De Vita E, et al. AJNR Am J Neuroradiol. 2013 Sep;34(9):1723-30. doi: 10.3174/ajnr.A3504. Epub 2013 Mar 28. AJNR Am J Neuroradiol. 2013. PMID: 23538406 Free PMC article.

3

Prospective 10-year surveillance of human prion diseases in Japan.

Nozaki I, Hamaguchi T, Sanjo N, Noguchi-Shinohara M, Sakai K, Nakamura Y, Sato T, Kitamoto T, Mizusawa H, Moriwaka F, Shiga Y, Kuroiwa Y, Nishizawa M, Kuzuhara S, Inuzuka T, Takeda M, Kuroda S, Abe K, Murai H, Murayama S, Tateishi J, Takumi I, Shirabe S, Harada M, Sadakane A, Yamada M. Nozaki I, et al. Brain. 2010 Oct;133(10):3043-57. doi: 10.1093/brain/awq216. Epub 2010 Sep 20. Brain. 2010. PMID: 20855418

4

[Etiology, pathology and diagnosis of prion diseases in humans].

Kretzschmar HA. Kretzschmar HA. Internist (Berl). 2002 Jun;43(6):716-22, 724-30. doi: 10.1007/s00108-002-0636-3. Internist (Berl). 2002. PMID: 12426727 Review. German. No abstract available.

5

Multiple prion types in the same brain: is a molecular diagnosis of CJD possible?

Dickson DW, Brown P. Dickson DW, et al. Neurology. 1999 Dec 10;53(9):1903-4. doi: 10.1212/wnl.53.9.1903. Neurology. 1999. PMID: 10599755 No abstract available.

6

Recent advances in the histo-molecular pathology of human prion disease.

Baiardi S, Rossi M, Capellari S, Parchi P. Baiardi S, et al. Brain Pathol. 2019 Mar;29(2):278-300. doi: 10.1111/bpa.12695. Epub 2019 Jan 22. Brain Pathol. 2019. PMID: 30588685 Free PMC article. Review.

7

Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation.

Alner K, Hyare H, Mead S, Rudge P, Wroe S, Rohrer JD, Ridgway GR, Ourselin S, Clarkson M, Hunt H, Fox NC, Webb T, Collinge J, Cipolotti L. Alner K, et al. J Neurol Neurosurg Psychiatry. 2012 Jan;83(1):109-14. doi: 10.1136/jnnp-2011-300167. Epub 2011 Aug 17. J Neurol Neurosurg Psychiatry. 2012. PMID: 21849340

8

The prion diseases.

Mastrianni JA, Roos RP. Mastrianni JA, et al. Semin Neurol. 2000;20(3):337-52. doi: 10.1055/s-2000-9396. Semin Neurol. 2000. PMID: 11051298 Review.

9

A prion disease with a novel 96-base pair insertional mutation in the prion protein gene.

Campbell TA, Palmer MS, Will RG, Gibb WR, Luthert PJ, Collinge J. Campbell TA, et al. Neurology. 1996 Mar;46(3):761-6. doi: 10.1212/wnl.46.3.761. Neurology. 1996. PMID: 8618679

10

The prion diseases.

Brown K, Mastrianni JA. Brown K, et al. J Geriatr Psychiatry Neurol. 2010 Dec;23(4):277-98. doi: 10.1177/0891988710383576. Epub 2010 Oct 11. J Geriatr Psychiatry Neurol. 2010. PMID: 20938044 Review.

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