Similar articles for PMID: 10889050

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1

Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews.

Colombo R. Colombo R. Am J Hum Genet. 2000 Aug;67(2):528-31. doi: 10.1086/303021. Am J Hum Genet. 2000. PMID: 10889050 Free PMC article. No abstract available.

2

Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt-Jakob Disease (CJD).

Won SY, Kim YC, Jeong BH. Won SY, et al. Int J Mol Sci. 2023 Oct 2;24(19):14831. doi: 10.3390/ijms241914831. Int J Mol Sci. 2023. PMID: 37834279 Free PMC article.

3

Prion Mutations in Republic of Republic of Korea, China, and Japan.

Kim DY, Shim KH, Bagyinszky E, An SSA. Kim DY, et al. Int J Mol Sci. 2022 Dec 30;24(1):625. doi: 10.3390/ijms24010625. Int J Mol Sci. 2022. PMID: 36614069 Free PMC article. Review.

4

Effects of the pathological E200K mutation on human prion protein: A computational screening and molecular dynamics approach.

Gharemirshamloo FR, Majumder R, Kumar S U, Doss C GP, Bamdad K, Frootan F, Un C. Gharemirshamloo FR, et al. J Cell Biochem. 2023 Feb;124(2):254-265. doi: 10.1002/jcb.30359. Epub 2022 Dec 24. J Cell Biochem. 2023. PMID: 36565210

5

Genetic Creutzfeldt-Jakob disease in Turkish Jews-demographic and clinical features.

Menendez L, Milo R, Cohen OS, Chapman J, Rosenmann H, Nitsan Z, Kahana E, Appel S. Menendez L, et al. Acta Neurol Scand. 2022 Nov;146(5):586-589. doi: 10.1111/ane.13684. Epub 2022 Aug 16. Acta Neurol Scand. 2022. PMID: 35974683

6

Creutzfeldt-Jakob disease associated with a T188K homozygous mutation in the prion protein gene: a case report and review of the literature.

Shan Y, Zhang J, Cen Y, Xu X, Tan R, Zhao J, Yu S. Shan Y, et al. Prion. 2022 Dec;16(1):14-18. doi: 10.1080/19336896.2022.2031719. Prion. 2022. PMID: 35130121 Free PMC article. Review.

7

Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification.

Baiardi S, Rossi M, Mammana A, Appleby BS, Barria MA, Calì I, Gambetti P, Gelpi E, Giese A, Ghetti B, Herms J, Ladogana A, Mikol J, Pal S, Ritchie DL, Ruf V, Windl O, Capellari S, Parchi P. Baiardi S, et al. Acta Neuropathol. 2021 Oct;142(4):707-728. doi: 10.1007/s00401-021-02350-y. Epub 2021 Jul 29. Acta Neuropathol. 2021. PMID: 34324063 Free PMC article.

8

Genetic Creutzfeldt-Jakob disease in Sardinia: a case series linked to the PRNP R208H mutation due to a single founder effect.

Melis M, Molari A, Floris G, Vascellari S, Balestrino L, Ladogana A, Poleggi A, Parchi P, Cossu G, Melis M, Orrù S, Defazio G. Melis M, et al. Neurogenetics. 2020 Oct;21(4):251-257. doi: 10.1007/s10048-020-00618-1. Epub 2020 May 26. Neurogenetics. 2020. PMID: 32458274

9

[Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course].

Takayanagi M, Suzuki K, Nakamura T, Hirata K, Satoh K, Kitamoto T. Takayanagi M, et al. Rinsho Shinkeigaku. 2018 Nov 28;58(11):682-687. doi: 10.5692/clinicalneurol.cn-001206. Epub 2018 Oct 27. Rinsho Shinkeigaku. 2018. PMID: 30369528 Japanese.

10

Rare E196A mutation in PRNP gene of 3 Chinese patients with Creutzfeldt-Jacob disease.

Shi Q, Zhou W, Chen C, Zhang BY, Xiao K, Wang Y, Dong XP. Shi Q, et al. Prion. 2016 Jul 3;10(4):331-7. doi: 10.1080/19336896.2016.1190897. Prion. 2016. PMID: 27310471 Free PMC article.

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