These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
433 related articles for article (PubMed ID: 24851016)
1. Genetic studies in human prion diseases. Jeong BH; Kim YS J Korean Med Sci; 2014 May; 29(5):623-32. PubMed ID: 24851016 [TBL] [Abstract][Full Text] [Related]
6. Prion Mutations in Republic of Republic of Korea, China, and Japan. Kim DY; Shim KH; Bagyinszky E; An SSA Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36614069 [TBL] [Abstract][Full Text] [Related]
7. Hereditary Human Prion Diseases: an Update. Schmitz M; Dittmar K; Llorens F; Gelpi E; Ferrer I; Schulz-Schaeffer WJ; Zerr I Mol Neurobiol; 2017 Aug; 54(6):4138-4149. PubMed ID: 27324792 [TBL] [Abstract][Full Text] [Related]
8. An overview of human prion diseases. Imran M; Mahmood S Virol J; 2011 Dec; 8():559. PubMed ID: 22196171 [TBL] [Abstract][Full Text] [Related]
9. Diagnostic accuracy of cerebrospinal fluid biomarkers in genetic prion diseases. Schmitz M; Villar-Piqué A; Hermann P; Escaramís G; Calero M; Chen C; Kruse N; Cramm M; Golanska E; Sikorska B; Liberski PP; Pocchiari M; Lange P; Stehmann C; Sarros S; Martí E; Baldeiras I; Santana I; Žáková D; Mitrová E; Dong XP; Collins S; Poleggi A; Ladogana A; Mollenhauer B; Kovacs GG; Geschwind MD; Sánchez-Valle R; Zerr I; Llorens F Brain; 2022 Apr; 145(2):700-712. PubMed ID: 35288744 [TBL] [Abstract][Full Text] [Related]
10. Genetic Prion Disease: Insight from the Features and Experience of China National Surveillance for Creutzfeldt-Jakob Disease. Shi Q; Chen C; Xiao K; Zhou W; Gao LP; Chen DD; Wu YZ; Wang Y; Hu C; Gao C; Dong XP Neurosci Bull; 2021 Nov; 37(11):1570-1582. PubMed ID: 34487324 [TBL] [Abstract][Full Text] [Related]
11. The prion diseases. Brown K; Mastrianni JA J Geriatr Psychiatry Neurol; 2010 Dec; 23(4):277-98. PubMed ID: 20938044 [TBL] [Abstract][Full Text] [Related]
12. The First Evaluation of Proteinase K-Resistant Prion Protein (PrP Won SY; Kim YC; Lee YN; Park CG; Kim WY; Jeong BH Medicina (Kaunas); 2022 Jul; 58(7):. PubMed ID: 35888666 [No Abstract] [Full Text] [Related]
13. Elevated E200K Somatic Mutation of the Prion Protein Gene ( Won SY; Kim YC; Jeong BH Int J Mol Sci; 2023 Oct; 24(19):. PubMed ID: 37834279 [TBL] [Abstract][Full Text] [Related]
15. The First Meta-Analysis of the M129V Single-Nucleotide Polymorphism (SNP) of the Prion Protein Gene ( Kim YC; Jeong BH Cells; 2021 Nov; 10(11):. PubMed ID: 34831353 [TBL] [Abstract][Full Text] [Related]
16. Genotype patterns and characteristics of PRNP in the Korean population. Moe Lee S; Ran Ju Y; Choi BY; Wook Hyeon J; Sun Park J; Kyeong Kim C; Yeon Kim S Prion; 2012; 6(4):375-82. PubMed ID: 22561193 [TBL] [Abstract][Full Text] [Related]
18. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases. Schmitz M; Lüllmann K; Zafar S; Ebert E; Wohlhage M; Oikonomou P; Schlomm M; Mitrova E; Beekes M; Zerr I Neurobiol Aging; 2014 May; 35(5):1177-88. PubMed ID: 24360565 [TBL] [Abstract][Full Text] [Related]
19. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. Takada LT; Kim MO; Cleveland RW; Wong K; Forner SA; Gala II; Fong JC; Geschwind MD Am J Med Genet B Neuropsychiatr Genet; 2017 Jan; 174(1):36-69. PubMed ID: 27943639 [TBL] [Abstract][Full Text] [Related]
20. Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases. Kosami K; Ae R; Hamaguchi T; Sanjo N; Tsukamoto T; Kitamoto T; Yamada M; Mizusawa H; Nakamura Y J Neurol Neurosurg Psychiatry; 2022 Jul; 93(7):779-784. PubMed ID: 35387866 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]