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Journal Abstract Search

322 related items for PubMed ID: 8618678

  • 1. Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.
    Chapman J, Arlazoroff A, Goldfarb LG, Cervenakova L, Neufeld MY, Werber E, Herbert M, Brown P, Gajdusek DC, Korczyn AD.
    Neurology; 1996 Mar; 46(3):758-61. PubMed ID: 8618678
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  • 2. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.
    Gambetti P, Parchi P, Petersen RB, Chen SG, Lugaresi E.
    Brain Pathol; 1995 Jan; 5(1):43-51. PubMed ID: 7767490
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  • 5. Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism.
    Monari L, Chen SG, Brown P, Parchi P, Petersen RB, Mikol J, Gray F, Cortelli P, Montagna P, Ghetti B.
    Proc Natl Acad Sci U S A; 1994 Mar 29; 91(7):2839-42. PubMed ID: 7908444
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  • 6. Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia.
    Taniwaki Y, Hara H, Doh-Ura K, Murakami I, Tashiro H, Yamasaki T, Shigeto H, Arakawa K, Araki E, Yamada T, Iwaki T, Kira J.
    J Neurol Neurosurg Psychiatry; 2000 Mar 29; 68(3):388. PubMed ID: 10787305
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  • 7. [Usefulness of molecular genetic analysis of the PRNP gene in patients with cerebellar ataxia: a new case of fatal familial insomnia].
    Marcaud V, Laplanche JL, Defontaines B, Beaudry P, Vital A, Vincent D, Sazdovitch V, Hauw JJ, Latinville D, Jung P, Vecchierini F, Degos CF.
    Rev Neurol (Paris); 2003 Feb 29; 159(2):199-202. PubMed ID: 12660573
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  • 11. Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.
    Schmitz M, Lüllmann K, Zafar S, Ebert E, Wohlhage M, Oikonomou P, Schlomm M, Mitrova E, Beekes M, Zerr I.
    Neurobiol Aging; 2014 May 29; 35(5):1177-88. PubMed ID: 24360565
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  • 12. Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression.
    Harder A, Jendroska K, Kreuz F, Wirth T, Schafranka C, Karnatz N, Théallier-Janko A, Dreier J, Lohan K, Emmerich D, Cervós-Navarro J, Windl O, Kretzschmar HA, Nürnberg P, Witkowski R.
    Am J Med Genet; 1999 Dec 03; 87(4):311-6. PubMed ID: 10588836
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  • 14. Creutzfeldt-Jakob disease with a novel insertion and codon 219 Lys/Lys polymorphism in PRNP.
    Nishida Y, Sodeyama N, Toru Y, Toru S, Kitamoto T, Mizusawa H.
    Neurology; 2004 Nov 23; 63(10):1978-9. PubMed ID: 15557533
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  • 16. Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene.
    Bratosiewicz J, Liberski PP, Kulczycki J, Kordek R.
    Acta Neurobiol Exp (Wars); 2001 Nov 23; 61(3):151-6. PubMed ID: 11584448
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  • 17. Reduced cerebral blood flow in genetic prion disease with PRNP D178N-129M mutation: an arterial spin labeling MRI study.
    Chen S, Guan M, Shang JK, He S, Zhang ML, Ma MM, Zhang JW.
    J Clin Neurosci; 2015 Jan 23; 22(1):204-6. PubMed ID: 25220284
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  • 18. [Genetic background of human prion diseases].
    Kovács GG.
    Ideggyogy Sz; 2007 Nov 30; 60(11-12):438-46. PubMed ID: 18198790
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