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Journal Abstract Search

266 related items for PubMed ID: 15558291

  • 1. Loss of glycosylation associated with the T183A mutation in human prion disease.
    Grasbon-Frodl E, Lorenz H, Mann U, Nitsch RM, Windl O, Kretzschmar HA.
    Acta Neuropathol; 2004 Dec; 108(6):476-84. PubMed ID: 15558291
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  • 2. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H.
    Acta Neuropathol; 2005 Nov; 110(5):513-9. PubMed ID: 16155763
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  • 3. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R, Rosemberg S, Passos-Bueno MR, da Silva LS, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBlanc A.
    Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
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  • 4. MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathology.
    Hoshino A, Iwasaki Y, Izumi M, Kimura S, Ibi T, Kitamoto T, Yoshida M, Hashizume Y, Sahashi K.
    Neuropathology; 2008 Jun; 28(3):326-32. PubMed ID: 18248577
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  • 5. Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment.
    Roeber S, Krebs B, Neumann M, Windl O, Zerr I, Grasbon-Frodl EM, Kretzschmar HA.
    Acta Neuropathol; 2005 Apr; 109(4):443-8. PubMed ID: 15739100
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  • 6. Creutzfeldt-Jakob disease with an M232R substitution: report of a patient showing slowly progressive disease with abundant plaque-like PrP deposits in the cerebellum.
    Shimizu H, Yamada M, Matsubara N, Takano H, Umeda Y, Kawase Y, Kitamoto T, Nishizawa M, Takahashi H.
    Neuropathology; 2009 Dec; 29(6):735-43. PubMed ID: 19422537
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  • 7. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
    Hama T, Iwasaki Y, Niwa H, Yoshida M, Hashizume Y, Kitamoto T, Murakami N, Sobue G.
    Neuropathology; 2009 Dec; 29(6):727-34. PubMed ID: 19422533
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  • 8. Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
    Casalone C, Zanusso G, Acutis P, Ferrari S, Capucci L, Tagliavini F, Monaco S, Caramelli M.
    Proc Natl Acad Sci U S A; 2004 Mar 02; 101(9):3065-70. PubMed ID: 14970340
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  • 10. V180I mutation of the prion protein gene associated with atypical PrPSc glycosylation.
    Chasseigneaux S, Haïk S, Laffont-Proust I, De Marco O, Lenne M, Brandel JP, Hauw JJ, Laplanche JL, Peoc'h K.
    Neurosci Lett; 2006 Nov 20; 408(3):165-9. PubMed ID: 17029785
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  • 11. An autopsy case of Creutzfeldt-Jakob disease with a V180I mutation of the PrP gene and Alzheimer-type pathology.
    Yoshida H, Terada S, Ishizu H, Ikeda K, Hayabara T, Ikeda K, Deguchi K, Touge T, Kitamoto T, Kuroda S.
    Neuropathology; 2010 Apr 20; 30(2):159-64. PubMed ID: 19703264
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  • 12. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
    Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H.
    Ann Neurol; 1999 Jun 20; 45(6):812-6. PubMed ID: 10360778
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  • 13. Distinctive cerebellar immunoreactivity for the prion protein in familial (E200K) Creutzfeldt-Jakob disease.
    Jarius C, Kovacs GG, Belay G, Hainfellner JA, Mitrova E, Budka H.
    Acta Neuropathol; 2003 May 20; 105(5):449-54. PubMed ID: 12677444
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  • 17. Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein gene.
    Capellari S, Cardone F, Notari S, Schininà ME, Maras B, Sità D, Baruzzi A, Pocchiari M, Parchi P.
    Neurology; 2005 Mar 08; 64(5):905-7. PubMed ID: 15753435
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  • 18. Accumulation of mono-glycosylated form-rich, plaque-forming PrPSc in the second atypical bovine spongiform encephalopathy case in Japan.
    Hagiwara K, Yamakawa Y, Sato Y, Nakamura Y, Tobiume M, Shinagawa M, Sata T.
    Jpn J Infect Dis; 2007 Sep 08; 60(5):305-8. PubMed ID: 17881874
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  • 20. [An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation].
    Matsumura T, Kojima S, Kuroiwa Y, Takagi A, Unakami M, Kitamoto T.
    Rinsho Shinkeigaku; 1995 Mar 08; 35(3):282-5. PubMed ID: 7614752
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