Similar articles for PMID: 23557959

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1

Inherited forms of Creutzfeldt-Jakob disease.

Degnan AJ, Levy LM. Degnan AJ, et al. AJNR Am J Neuroradiol. 2013 Sep;34(9):1690-1. doi: 10.3174/ajnr.A3580. Epub 2013 Apr 4. AJNR Am J Neuroradiol. 2013. PMID: 23557959 Free PMC article. No abstract available.

2

Evidence of a new human genotype susceptible to variant CJD.

Ward HJ. Ward HJ. Euro Surveill. 2006 Jun 1;11(6):E060601.3. doi: 10.2807/esw.11.22.02965-en. Euro Surveill. 2006. PMID: 16819115 No abstract available.

3

Are further genetic factors associated with the risk of developing variant Creutzfeldt-Jakob disease?

Kretzschmar H, Illig T. Kretzschmar H, et al. Lancet Neurol. 2009 Jan;8(1):25-6. doi: 10.1016/S1474-4422(08)70266-7. Lancet Neurol. 2009. PMID: 19081509 No abstract available.

4

[Mad cow disease and new form of Creutzfeldt-Jakob disease: state of the art].

Nau Jewan-Yves. Nau Jewan-Yves. Rev Med Suisse. 2014 Nov 5;10(449):2114-5. Rev Med Suisse. 2014. PMID: 25536833 Review. French. No abstract available.

5

Sporadic Creutzfeldt-Jakob disease: further twists and turns in a convoluted protein.

Head MW, Ironside JW. Head MW, et al. Brain. 2006 Sep;129(Pt 9):2238-40. doi: 10.1093/brain/awl225. Brain. 2006. PMID: 16923953 No abstract available.

6

Creutzfeldt-Jakob disease and related disorders: etiopathogenetic aspects.

Barbanti P, Pocchiari M. Barbanti P, et al. Funct Neurol. 1997 May-Aug;12(3-4):159-64. Funct Neurol. 1997. PMID: 9218970 Review. No abstract available.

7

Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment.

Jeong BH, Jeon YC, Lee YJ, Cho HJ, Park SJ, Chung DI, Kim J, Kim SH, Kim HT, Choi EK, Choi KC, Carp RI, Kim YS. Jeong BH, et al. Neuropathol Appl Neurobiol. 2010 Oct;36(6):558-63. doi: 10.1111/j.1365-2990.2010.01094.x. Neuropathol Appl Neurobiol. 2010. PMID: 20497338 No abstract available.

8

Sporadic--but not variant--Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1.

Mead S, Mahal SP, Beck J, Campbell T, Farrall M, Fisher E, Collinge J. Mead S, et al. Am J Hum Genet. 2001 Dec;69(6):1225-35. doi: 10.1086/324710. Epub 2001 Nov 5. Am J Hum Genet. 2001. PMID: 11704923 Free PMC article.

9

Examination of the human prion protein-like gene doppel for genetic susceptibility to sporadic and variant Creutzfeldt-Jakob disease.

Mead S, Beck J, Dickinson A, Fisher EM, Collinge J. Mead S, et al. Neurosci Lett. 2000 Aug 25;290(2):117-20. doi: 10.1016/s0304-3940(00)01319-7. Neurosci Lett. 2000. PMID: 10936691

10

Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.

Ito Y, Sanjo N, Hizume M, Kobayashi A, Ohgami T, Satoh K, Hamaguchi T, Yamada M, Kitamoto T, Mizusawa H, Yokota T. Ito Y, et al. Biochem Biophys Res Commun. 2018 Feb 19;496(4):1055-1061. doi: 10.1016/j.bbrc.2018.01.119. Epub 2018 Jan 31. Biochem Biophys Res Commun. 2018. PMID: 29382530

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