161 related articles for article (PubMed ID: 35738080)
1. Thalamic-insomnia phenotype in E200K Creutzfeldt-Jakob disease: A PET/MRI study.
Ye H; Chu M; Chen Z; Xie K; Liu L; Nan H; Cui Y; Zhang J; Wang L; Li J; Wu L
Neuroimage Clin; 2022; 35():103086. PubMed ID: 35738080
[TBL] [Abstract][Full Text] [Related]
2. 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
Acta Neuropathol; 2021 Oct; 142(4):707-728. PubMed ID: 34324063
[TBL] [Abstract][Full Text] [Related]
3. The insomnia phenotype in genetic Creutzfeldt-Jakob disease based on the E200K mutation.
Feketeova E; Jarcuskova D; Janakova A; Vitkova M; Dragasek J; Gdovinova Z
Prion; 2019 Jan; 13(1):77-82. PubMed ID: 30922182
[TBL] [Abstract][Full Text] [Related]
4. Creutzfeldt-Jakob disease surveillance in Eastern Slovakia from 2004 to 2016.
Feketeová E; Jarčušková D; Janáková A; Rozprávková E; Cifráková Z; Farkašová-Inaccone S; Rimárová K; Dorko E; Gdovinová Z
Cent Eur J Public Health; 2018 Dec; 26 Suppl():S37-S41. PubMed ID: 30817871
[TBL] [Abstract][Full Text] [Related]
5. Magnetic resonance imaging in E200K and V210I mutations of the prion protein gene.
Breithaupt M; Romero C; Kallenberg K; Begue C; Sanchez-Juan P; Eigenbrod S; Kretzschmar H; Schelzke G; Meichtry E; Taratuto A; Zerr I
Alzheimer Dis Assoc Disord; 2013; 27(1):87-90. PubMed ID: 22407223
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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
Prion; 2022 Dec; 16(1):14-18. PubMed ID: 35130121
[TBL] [Abstract][Full Text] [Related]
8. The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol.
Bregman N; Shiner T; Kavé G; Alcalay R; Gana-Weisz M; Goldstein O; Glinka T; Aizenstein O; Bashat DB; Alcalay Y; Mirelman A; Thaler A; Giladi N; Omer N
BMC Neurol; 2023 Apr; 23(1):151. PubMed ID: 37069531
[TBL] [Abstract][Full Text] [Related]
9. Cerebral cortex swelling in V180I genetic Creutzfeldt-Jakob disease: comparative imaging study between sporadic and V180I genetic Creutzfeldt-Jakob disease in the early stage.
Muroga Y; Sugiyama A; Mukai H; Hashiba J; Yokota H; Satoh K; Kitamoto T; Wang J; Ito S; Kuwabara S
Prion; 2023 Dec; 17(1):105-110. PubMed ID: 37013454
[TBL] [Abstract][Full Text] [Related]
10. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.
Taratuto AL; Piccardo P; Reich EG; Chen SG; Sevlever G; Schultz M; Luzzi AA; Rugiero M; Abecasis G; Endelman M; Garcia AM; Capellari S; Xie Z; Lugaresi E; Gambetti P; Dlouhy SR; Ghetti B
Neurology; 2002 Feb; 58(3):362-7. PubMed ID: 11839833
[TBL] [Abstract][Full Text] [Related]
11. The genetic Creutzfeldt-Jakob disease with E200K mutation: analysis of clinical, genetic and laboratory features of 30 Chinese patients.
Gao LP; Shi Q; Xiao K; Wang J; Zhou W; Chen C; Dong XP
Sci Rep; 2019 Feb; 9(1):1836. PubMed ID: 30755683
[TBL] [Abstract][Full Text] [Related]
12. Quantitative Magnetic Resonance Abnormalities in Creutzfeldt-Jakob Disease and Fatal Insomnia.
Grau-Rivera O; Calvo A; Bargalló N; Monté GC; Nos C; Lladó A; Molinuevo JL; Gelpi E; Sánchez-Valle R
J Alzheimers Dis; 2017; 55(1):431-443. PubMed ID: 27662320
[TBL] [Abstract][Full Text] [Related]
13. A longitudinal
Chu M; Chen Z; Nie B; Liu L; Xie K; Cui Y; Chen K; Rosa-Neto P; Wu L
J Neurol; 2022 Nov; 269(11):6094-6103. PubMed ID: 35864212
[TBL] [Abstract][Full Text] [Related]
14. Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease.
Hamaguchi T; Kitamoto T; Sato T; Mizusawa H; Nakamura Y; Noguchi M; Furukawa Y; Ishida C; Kuji I; Mitani K; Murayama S; Kohriyama T; Katayama S; Yamashita M; Yamamoto T; Udaka F; Kawakami A; Ihara Y; Nishinaka T; Kuroda S; Suzuki N; Shiga Y; Arai H; Maruyama M; Yamada M
Neurology; 2005 Feb; 64(4):643-8. PubMed ID: 15728285
[TBL] [Abstract][Full Text] [Related]
15. Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.
Mitrová E; Belay G
Acta Virol; 2002; 46(1):31-9. PubMed ID: 12197632
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Creutzfeldt-Jakob encephalopathy with mutation E200K. Report of a "sporadic" case].
Cosacov RM; Taratuto AL; Ghiraridi G; Barrionuevo P; Diaz A; Begué C; Martinetto H
Rev Fac Cien Med Univ Nac Cordoba; 2004; 61(1):48-53. PubMed ID: 15366237
[TBL] [Abstract][Full Text] [Related]
18. Systematic Review of Clinical and Pathophysiological Features of Genetic Creutzfeldt-Jakob Disease Caused by a Val-to-Ile Mutation at Codon 180 in the Prion Protein Gene.
Matsubayashi T; Sanjo N
Int J Mol Sci; 2022 Dec; 23(23):. PubMed ID: 36499498
[TBL] [Abstract][Full Text] [Related]
19. Intraneuronal immunoreactivity for the prion protein distinguishes a subset of E200K genetic from sporadic Creutzfeldt-Jakob Disease.
Kovacs GG; Molnár K; Keller E; Botond G; Budka H; László L
J Neuropathol Exp Neurol; 2012 Mar; 71(3):223-32. PubMed ID: 22318125
[TBL] [Abstract][Full Text] [Related]
20. The EEG in E200K familial CJD: relation to MRI patterns.
Appel SA; Chapman J; Prohovnik I; Hoffman C; Cohen OS; Blatt I
J Neurol; 2012 Mar; 259(3):491-6. PubMed ID: 21833705
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
