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Journal Abstract Search

393 related items for PubMed ID: 22411239

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  • 2. Gerstmann-Sträussler-Scheinker disease. I. Human diseases.
    Liberski PP, Budka H.
    Folia Neuropathol; 2004; 42 Suppl B():120-40. PubMed ID: 16903147
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  • 3. 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
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  • 4. 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 01; 70(9):1180-5. PubMed ID: 23857164
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  • 9. Hereditary prion protein amyloidoses.
    Ghetti B, Tagliavini F, Takao M, Bugiani O, Piccardo P.
    Clin Lab Med; 2003 Mar 01; 23(1):65-85, viii. PubMed ID: 12733425
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  • 10. Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker.
    Ghetti B, Piccardo P, Zanusso G.
    Handb Clin Neurol; 2018 Mar 01; 153():243-269. PubMed ID: 29887140
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  • 11. Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.
    Ghetti B, Dlouhy SR, Giaccone G, Bugiani O, Frangione B, Farlow MR, Tagliavini F.
    Brain Pathol; 1995 Jan 01; 5(1):61-75. PubMed ID: 7767492
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  • 16. Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles.
    Bruno R, Pirisinu L, Riccardi G, D'Agostino C, De Cecco E, Legname G, Cardone F, Gambetti P, Nonno R, Agrimi U, Di Bari MA.
    Biomolecules; 2022 Oct 21; 12(10):. PubMed ID: 36291746
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  • 17. A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration.
    Alzualde A, Indakoetxea B, Ferrer I, Moreno F, Barandiaran M, Gorostidi A, Estanga A, Ruiz I, Calero M, van Leeuwen FW, Atares B, Juste R, Rodriguez-Martínez AB, López de Munain A.
    J Neuropathol Exp Neurol; 2010 Aug 21; 69(8):789-800. PubMed ID: 20613639
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  • 18. 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 21; 45(6):1127-34. PubMed ID: 7783876
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  • 19. 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 21; 18(12):e152-3. PubMed ID: 22097954
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  • 20. 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 21; 57(10):979-88. PubMed ID: 9786248
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