BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 37325010)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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 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]  

  • 6. 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]  

  • 7. Gerstmann-Sträussler-Scheinker Disease Presenting as Late-Onset Slowly Progressive Spinocerebellar Ataxia, and Comparative Case Series with Neuropathology.
    Stephen CD; de Gusmao CM; Srinivasan SR; Olsen A; Freua F; Kok F; Montes Garcia Barbosa R; Chen JYH; Appleby BS; Prior T; Frosch MP; Schmahmann JD
    Mov Disord Clin Pract; 2024 Apr; 11(4):411-423. PubMed ID: 38258626
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Familial Prion Disease: First Indian Kindred with Gerstmann-Sträussler-Scheinker Syndrome.
    Bhatia S; Bijarnia-Mahay S; Dubey S; Gourie-Devi M
    Neurol India; 2020; 68(6):1431-1434. PubMed ID: 33342883
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gerstmann-Sträussler-Scheinker syndrome misdiagnosed as cervical spondylotic myelopathy: A case report with 5-year follow-up.
    Cao L; Feng H; Huang X; Yi J; Zhou Y
    Medicine (Baltimore); 2021 Apr; 100(16):e25687. PubMed ID: 33879752
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Gerstmann-Sträussler-Scheinker disease: A case report.
    Zhao MM; Feng LS; Hou S; Shen PP; Cui L; Feng JC
    World J Clin Cases; 2019 Feb; 7(3):389-395. PubMed ID: 30746381
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [
    Risacher SL; Farlow MR; Bateman DR; Epperson F; Tallman EF; Richardson R; Murrell JR; Unverzagt FW; Apostolova LG; Bonnin JM; Ghetti B; Saykin AJ
    Acta Neuropathol Commun; 2018 Oct; 6(1):114. PubMed ID: 30373672
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. 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]  

  • 18. Accumulation Area of a Japanese
    Suzuyama K; Eriguchi M; Minagawa H; Honda H; Kai K; Kitamoto T; Hara H
    J Clin Neurol; 2024 May; 20(3):321-329. PubMed ID: 38171504
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Clinical features of Chinese patients with Gerstmann-Sträussler-Scheinker identified by targeted next-generation sequencing.
    Li HF; Liu ZJ; Dong HL; Xie JJ; Zhao SY; Ni W; Dong Y; Wu ZY
    Neurobiol Aging; 2017 Jan; 49():216.e1-216.e5. PubMed ID: 28340953
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.