158 related articles for article (PubMed ID: 20386644)
1. A case of gerstmann-sträussler-scheinker disease.
Park MJ; Jo HY; Cheon SM; Choi SS; Kim YS; Kim JW
J Clin Neurol; 2010 Mar; 6(1):46-50. PubMed ID: 20386644
[TBL] [Abstract][Full Text] [Related]
2. Serial changes in regional cerebral blood flow in Gerstmann-Sträussler-Scheinker disease caused by a Pro-to-Leu mutation at codon 105 in the prion protein gene.
Kawai H; Matsubayashi T; Yokota T; Sanjo N
Prion; 2023 Dec; 17(1):138-140. PubMed ID: 37705331
[TBL] [Abstract][Full Text] [Related]
3. [Patient with Gerstmann-Striussler-Scheinker syndrome (GSS P102L) presenting high intensity lesions in the cerebral cortex on diffusion weighted MRI].
Misumi M; Nishida Y; Araki S
Rinsho Shinkeigaku; 2006 Apr; 46(4):291-3. PubMed ID: 16768100
[TBL] [Abstract][Full Text] [Related]
4. First familial cases of P102L Gerstmann-Sträussler-Scheinker syndrome in South Korea: diffusion-weighted imaging might reflect intrafamilial phenotypic variability.
Ahn SJ; Lee HS; Moon J; Chu K
Neurol Sci; 2022 May; 43(5):3419-3422. PubMed ID: 35129726
[TBL] [Abstract][Full Text] [Related]
5. [Case of Gerstmann-Sträussler-Scheinker syndrome (GSS-P102L) mimicking variant Creurtzfeldt-Jakob disease in clinical manifestation and MRI findings].
Kanata A; Saigoh K; Mitsui Y; Kitamoto T; Kusunoki S
Rinsho Shinkeigaku; 2008 Mar; 48(3):179-83. PubMed ID: 18409537
[TBL] [Abstract][Full Text] [Related]
6. A Chinese patient of P102L Gerstmann-Sträussler-Scheinker disease contains three other disease-associated mutations in SYNE1.
Wang J; Xiao K; Zhou W; Gao C; Chen C; Shi Q; Dong XP
Prion; 2018 Mar; 12(2):150-155. PubMed ID: 29509064
[TBL] [Abstract][Full Text] [Related]
7. Gerstmann-Sträussler-Scheinker disease.
Liberski PP
Adv Exp Med Biol; 2012; 724():128-37. PubMed ID: 22411239
[TBL] [Abstract][Full Text] [Related]
8. A distinct phenotype of leg hyperreflexia in a Japanese family with Gerstmann-Sträussler-Scheinker syndrome (P102L).
Takazawa T; Ikeda K; Ito H; Aoyagi J; Nakamura Y; Miura K; Iwamoto K; Kano O; Kawabe K; Iwasaki Y
Intern Med; 2010; 49(4):339-42. PubMed ID: 20154442
[TBL] [Abstract][Full Text] [Related]
9. A case of Gerstmann-Sträussler-Scheinker syndrome.
Irisawa M; Amanuma M; Kozawa E; Kimura F; Araki N
Magn Reson Med Sci; 2007; 6(1):53-7. PubMed ID: 17510542
[TBL] [Abstract][Full Text] [Related]
10. A family with mental disorder as the first symptom finally confirmed with Gerstmann-Sträussler-Scheinker disease with P102L mutation in PRNP gene - case report.
Chen Z; Guo J; Ran N; Zhong Y; Yang F; Sun H
Prion; 2023 Dec; 17(1):37-43. PubMed ID: 36847171
[TBL] [Abstract][Full Text] [Related]
11. Case report: A Chinese patient with spinocerebellar ataxia finally confirmed as Gerstmann-Sträussler-Scheinker syndrome with P102L mutation.
Chen L; Xu Y; Fang MJ; Shi YG; Zhang J; Zhang LL; Wang Y; Han YZ; Hu JY; Yang RM; Yu XE
Front Neurol; 2023; 14():1187813. PubMed ID: 37602242
[TBL] [Abstract][Full Text] [Related]
12. Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation.
Riudavets MA; Sraka MA; Schultz M; Rojas E; Martinetto H; Begué C; Noher de Halac I; Poleggi A; Equestre M; Pocchiari M; Sevlever G; Taratuto AL
Brain Pathol; 2014 Mar; 24(2):142-7. PubMed ID: 23944754
[TBL] [Abstract][Full Text] [Related]
13. Gerstmann-Sträussler-Scheinker Disease: A Case Report.
Shin M; Kim D; Heo YJ; Baek JW; Yun S; Jeong HW
J Korean Soc Radiol; 2023 May; 84(3):745-749. PubMed ID: 37325010
[TBL] [Abstract][Full Text] [Related]
14. Analysis of 12 Chinese Patients with Proline-to-Leucine Mutation at Codon 102-Associated Gerstmann-Sträussler-Scheinker Disease.
Wang J; Xiao K; Zhou W; Shi Q; Dong XP
J Clin Neurol; 2019 Apr; 15(2):184-190. PubMed ID: 30877692
[TBL] [Abstract][Full Text] [Related]
15. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
Sasaki K; Doh-ura K; Furuta A; Nakashima S; Morisada Y; Tateishi J; Iwaki T
Acta Neuropathol; 2003 Jul; 106(1):92-6. PubMed ID: 12682740
[TBL] [Abstract][Full Text] [Related]
16. A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
Long L; Cai X; Shu Y; Lu Z
Neurosciences (Riyadh); 2017 Apr; 22(2):138-142. PubMed ID: 28416787
[TBL] [Abstract][Full Text] [Related]
17. Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family.
Giovagnoli AR; Di Fede G; Aresi A; Reati F; Rossi G; Tagliavini F
Neurol Sci; 2008 Dec; 29(6):405-10. PubMed ID: 19030774
[TBL] [Abstract][Full Text] [Related]
18. Quantitative, functional MRI and neurophysiological markers in a case of Gerstmann-Sträussler-Scheinker syndrome.
Marino S; Morabito R; De Salvo S; Bonanno L; Bramanti A; Pollicino P; Giorgianni R; Bramanti P
Funct Neurol; 2017; 32(3):153-158. PubMed ID: 29042004
[TBL] [Abstract][Full Text] [Related]
19. Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients.
Young K; Jones CK; Piccardo P; Lazzarini A; Golbe LI; Zimmerman TR; Dickson DW; McLachlan DC; St George-Hyslop P; Lennox A
Neurology; 1995 Jun; 45(6):1127-34. PubMed ID: 7783876
[TBL] [Abstract][Full Text] [Related]
20. A case of Gerstmann-Straussler-Scheinker (GSS) disease with supranuclear gaze palsy.
Ufkes NA; Woodard C; Dale ML
J Clin Mov Disord; 2019; 6():7. PubMed ID: 31890235
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
