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Journal Abstract Search

404 related items for PubMed ID: 32946318

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  • 2. 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; 22(1):204-6. PubMed ID: 25220284
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  • 3. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.
    Komatsu J, Sakai K, Hamaguchi T, Sugiyama Y, Iwasa K, Yamada M.
    Prion; 2014 Jan; 8(5):336-8. PubMed ID: 25495585
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  • 4. Phenotypic variability in fatal familial insomnia (D178N-129M) genotype.
    Zerr I, Giese A, Windl O, Kropp S, Schulz-Schaeffer W, Riedemann C, Skworc K, Bodemer M, Kretzschmar HA, Poser S.
    Neurology; 1998 Nov; 51(5):1398-405. PubMed ID: 9818868
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  • 5. 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; 68(3):388. PubMed ID: 10787305
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  • 6. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G.
    Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
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  • 12. Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.
    Sun L, Li X, Lin X, Yan F, Chen K, Xiao S.
    Prion; 2015 Mar; 9(3):228-35. PubMed ID: 26074146
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  • 13. Diffusion-weighted imaging negative M232R familial Creutzfeldt-Jakob disease.
    Kang YJ, Kim KH, Jang SH, Lee GH, Lee YJ, Kim YS, Kim EJ.
    J Clin Neurosci; 2019 Jun; 64():47-49. PubMed ID: 30910549
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  • 17. Iatrogenic CJD due to pituitary-derived growth hormone with genetically determined incubation times of up to 40 years.
    Rudge P, Jaunmuktane Z, Adlard P, Bjurstrom N, Caine D, Lowe J, Norsworthy P, Hummerich H, Druyeh R, Wadsworth JD, Brandner S, Hyare H, Mead S, Collinge J.
    Brain; 2015 Nov; 138(Pt 11):3386-99. PubMed ID: 26268531
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