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Journal Abstract Search

200 related items for PubMed ID: 9030710

  • 1. Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.
    Young K, Clark HB, Piccardo P, Dlouhy SR, Ghetti B.
    Brain Res Mol Brain Res; 1997 Feb; 44(1):147-50. PubMed ID: 9030710
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  • 2. 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
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  • 9. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
    Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B.
    Nat Genet; 1992 Apr; 1(1):64-7. PubMed ID: 1363809
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  • 10. 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
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  • 14. A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxia.
    Cagnoli C, Brussino A, Sbaiz L, Di Gregorio E, Atzori C, Caroppo P, Orsi L, Migone N, Buffa C, Imperiale D, Brusco A.
    Mov Disord; 2008 Jul 30; 23(10):1468-71. PubMed ID: 18566986
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  • 16. 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 30; 106(1):92-6. PubMed ID: 12682740
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  • 18. 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 30; 17(1):138-140. PubMed ID: 37705331
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  • 19. A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome.
    Hsiao KK, Cass C, Schellenberg GD, Bird T, Devine-Gage E, Wisniewski H, Prusiner SB.
    Neurology; 1991 May 30; 41(5):681-4. PubMed ID: 1674116
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  • 20. De novo P102L mutation in a patient with Gerstmann-Sträussler-Scheinker disease.
    Kojović M, Glavač D, Ožek B, Zupan A, Popović M.
    Eur J Neurol; 2011 Dec 30; 18(12):e152-3. PubMed ID: 22097954
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