BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 17510542)

  • 21. Gerstmann-Sträussler-Scheinker disease. I. Human diseases.
    Liberski PP; Budka H
    Folia Neuropathol; 2004; 42 Suppl B():120-40. PubMed ID: 16903147
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.
    Iwasaki Y; Kizawa M; Hori N; Kitamoto T; Sobue G
    Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature.
    Rusina R; Fiala J; Holada K; Matějčková M; Nováková J; Ampapa R; Koukolík F; Matěj R
    Neurocase; 2013; 19(1):41-53. PubMed ID: 22494260
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu).
    Arata H; Takashima H; Hirano R; Tomimitsu H; Machigashira K; Izumi K; Kikuno M; Ng AR; Umehara F; Arisato T; Ohkubo R; Nakabeppu Y; Nakajo M; Osame M; Arimura K
    Neurology; 2006 Jun; 66(11):1672-8. PubMed ID: 16769939
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome.
    Tesar A; Matej R; Kukal J; Johanidesova S; Rektorova I; Vyhnalek M; Keller J; Eliasova I; Parobkova E; Smetakova M; Musova Z; Rusina R
    Ann Neurol; 2019 Nov; 86(5):643-652. PubMed ID: 31397917
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Transmissibility of Gerstmann-Sträussler-Scheinker syndrome in rodent models: New insights into the molecular underpinnings of prion infectivity.
    Nonno R; Angelo Di Bari M; Agrimi U; Pirisinu L
    Prion; 2016 Nov; 10(6):421-433. PubMed ID: 27892798
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.
    Collins S; McLean CA; Masters CL
    J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Support of linkage of Gerstmann-Sträussler-Scheinker syndrome to the prion protein gene on chromosome 20p12-pter.
    Speer MC; Goldgaber D; Goldfarb LG; Roses AD; Pericak-Vance MA
    Genomics; 1991 Feb; 9(2):366-8. PubMed ID: 1672296
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Sleep and temperature rhythms in two sisters with P102L Gerstmann-Sträussler-Scheinker (GSS) disease.
    Provini F; Vetrugno R; Pierangeli G; Cortelli P; Rizzo G; Filla A; Strisciuglio C; Gallassi R; Montagna P
    Sleep Med; 2009 Mar; 10(3):374-7. PubMed ID: 18550428
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
    Simpson M; Johanssen V; Boyd A; Klug G; Masters CL; Li QX; Pamphlett R; McLean C; Lewis V; Collins SJ
    JAMA Neurol; 2013 Sep; 70(9):1180-5. PubMed ID: 23857164
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [A case of Gerstmann-Sträussler-Scheinker disease presented with numbness in the lower extremities].
    Ando R; Nagai M; Iwaki H; Yabe H; Nishikawa N; Nomoto M
    Rinsho Shinkeigaku; 2016; 56(1):7-11. PubMed ID: 26616483
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mathematical models for the diffusion magnetic resonance signal abnormality in patients with prion diseases.
    Figini M; Alexander DC; Redaelli V; Fasano F; Grisoli M; Baselli G; Gambetti P; Tagliavini F; Bizzi A
    Neuroimage Clin; 2015; 7():142-54. PubMed ID: 25610776
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Spongiform encephalopathy transmitted experimentally from Creutzfeldt-Jakob and familial Gerstmann-Sträussler-Scheinker diseases.
    Baker HF; Duchen LW; Jacobs JM; Ridley RM
    Brain; 1990 Dec; 113 ( Pt 6)():1891-909. PubMed ID: 2276050
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Different Complicated Brain Pathologies in Monozygotic Twins With Gerstmann-Sträussler-Scheinker Disease.
    Honda H; Sasaki K; Takashima H; Mori D; Koyama S; Suzuki SO; Iwaki T
    J Neuropathol Exp Neurol; 2017 Oct; 76(10):854-863. PubMed ID: 28922846
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia.
    Ishizawa K; Komori T; Shimazu T; Yamamoto T; Kitamoto T; Shimazu K; Hirose T
    Acta Neuropathol; 2002 Oct; 104(4):342-50. PubMed ID: 12200619
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
    Piccardo P; Dlouhy SR; Lievens PM; Young K; Bird TD; Nochlin D; Dickson DW; Vinters HV; Zimmerman TR; Mackenzie IR; Kish SJ; Ang LC; De Carli C; Pocchiari M; Brown P; Gibbs CJ; Gajdusek DC; Bugiani O; Ironside J; Tagliavini F; Ghetti B
    J Neuropathol Exp Neurol; 1998 Oct; 57(10):979-88. PubMed ID: 9786248
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.