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Choroba Creutzfeldta-Jakoba (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Choroba Creutzfeldta-Jakoba" in Polish language version.

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  • Jakob A. Über eigenartige Erkrankungen des Zentralnervensystems mit bemerkenswertem anatomischen Befunde (Spastische Pseudosklerose – Encephalomyclopathie mit disseminirrten Degenerationsherden). „Zeitschrift für die gesamte Neurologie und Psychiatrie”. 64 (1), s. 147-228, 1921. DOI: 10.1007/BF02870932. 
  • Creutzfeldt H.G.. Über eine eigenartige herdförmige Erkrankung des Zentralnervensystems (vorläufige Mitteilung). „Zeitschrift für die gesamte Neurologie und Psychiatrie”. 57, s. 1-18, 1920. DOI: 10.1007/BF02866081. 
  • Kirschbaum W.. Zwei eigenartige Erkrankungen des Zentralnervensystems nach Art der spastischen Pseudosklerose (Jakob). „Zeitschrift für die gesamte Neurologie und Psychiatrie”. 92 (1), s. 175–220, 1924. DOI: 10.1007/BF02877841. 
  • Heidenhain A. Klinische und anatomische Untersuchungen über eine eigenartige organische Erkrankung des Zentralnervensystems im Praesenium. „Zeitschrift für die gesamte Neurologie und Psychiatrie”. 118, s. 49–114, 1929. DOI: 10.1007/BF02892896. 
  • R.G. Will, J.W. Ironside, M. Zeidler, S.N. Cousens i inni. A new variant of Creutzfeldt-Jakob disease in the UK. „Lancet”. 347 (9006), s. 921–925, 1996. DOI: 10.1016/S0140-6736(96)91412-9. PMID: 8598754. 
  • Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. „Nat Genet”. 1. 1, s. 68-71, 1993. DOI: 10.1038/ng0492-68. PMID: 1363810. 
  • Kotta K, Paspaltsis I, Bostantjopoulou S, Latsoudis H, Plaitakis A, Kazis D, Collinge J, Sklaviadis T. Novel mutation of the PRNP gene of a clinical CJD case. „BMC Infect Dis”. 6, s. 169, 2006. DOI: 10.1186/1471-2334-6-169. PMID: 17129366. 
  • Tschampa HJ, Zerr I, Urbach H. Radiological assessment of Creutzfeldt-Jakob disease.. „Eur Radiol”. 17. 5, s. 1200-11, 2007. DOI: 10.1007/s00330-006-0456-2. PMID: 17093966. 

medscape.com

emedicine.medscape.com

nih.gov

ncbi.nlm.nih.gov

  • R.G. Will, J.W. Ironside, M. Zeidler, S.N. Cousens i inni. A new variant of Creutzfeldt-Jakob disease in the UK. „Lancet”. 347 (9006), s. 921–925, 1996. DOI: 10.1016/S0140-6736(96)91412-9. PMID: 8598754. 
  • Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J. A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease. „Neurology”. 43. 12, s. 2723-4, 1994. PMID: 7902972. 
  • Doh-ura K, Tateishi J, Sasaki H, Kitamoto T, Sakaki Y. Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. „Biochem Biophys Res Commun”. 163. 2, s. 974-9, 1989. PMID: 2783132. 
  • Mallucci GR, Campbell TA, Dickinson A, Beck J, Holt M, Plant G, de Pauw KW, Hakin RN, Clarke CE, Howell S, Davies-Jones GA, Lawden M, Smith CM, Ince P, Ironside JW, Bridges LR, Dean A, Weeks I, Collinge J. Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.. „Brain”. 122 ( Pt 10), s. 1823-37, 1999. PMID: 10506086. 
  • Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome. „Biochem Biophys Res Commun”. 191. 2, s. 709-14, 1993. PMID: 8461023. 
  • Jin K, Shiga Y, Shibuya S, Chida K, Sato Y, Konno H, Doh-ura K, Kitamoto T, Itoyama Y. Clinical features of Creutzfeldt-Jakob disease with V180I mutation. „Neurology”. 62. 3, s. 502-5, 2004. PMID: 14872044. 
  • Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles. „Nat Genet”. 1. 1, s. 68-71, 1993. DOI: 10.1038/ng0492-68. PMID: 1363810. 
  • Goldfarb LG, Mitrová E, Brown P, Toh BK, Gajdusek DC. Mutation in codon 200 of scrapie amyloid protein gene in two clusters of Creutzfeldt-Jakob disease in Slovakia. „Lancet”. 336. 8713, s. 514-5, 1990. PMID: 1975028. 
  • Beck JA, Mead S, Campbell TA, Dickinson A, Wientjens DP, Croes EA, Van Duijn CM, Collinge J. Two-octapeptide repeat deletion of prion protein associated with rapidly progressive dementia. „Neurology”. 57. 2, s. 354-6, 2001. PMID: 11468331. 
  • Cochran EJ, Bennett DA, Cervenáková L, Kenney K, Bernard B, Foster NL, Benson DF, Goldfarb LG, Brown P. Familial Creutzfeldt-Jakob disease with a five-repeat octapeptide insert mutation. „Neurology”. 47. 3, s. 727-33, 1996. PMID: 8797471. 
  • Brown P, Goldfarb LG, McCombie WR, Nieto A, Squillacote D, Sheremata W, Little BW, Godec MS, Gibbs CJ, Gajdusek DC. Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene. „Neurology”. 42. 2, s. 422-7, 1992. PMID: 1736177. 
  • Goldfarb LG, Brown P, McCombie WR, Goldgaber D, Swergold GD, Wills PR, Cervenakova L, Baron H, Gibbs CJ, Gajdusek DC. Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. „Proc Natl Acad Sci U S A”. 88. 23, s. 10926-30, 1992. PMID: 1683708. 
  • Krasemann S, Zerr I, Weber T, Poser S, Kretzschmar H, Hunsmann G, Bodemer W. Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene. „Brain Res Mol Brain Res”. 34. 1, s. 173-6, 1997. PMID: 8750875. 
  • Kotta K, Paspaltsis I, Bostantjopoulou S, Latsoudis H, Plaitakis A, Kazis D, Collinge J, Sklaviadis T. Novel mutation of the PRNP gene of a clinical CJD case. „BMC Infect Dis”. 6, s. 169, 2006. DOI: 10.1186/1471-2334-6-169. PMID: 17129366. 
  • Gálvez S., Cartier L.. Computed tomography findings in 15 cases of Creutzfeldt-Jakob disease with histological verification. „J Neurol Neurosurg Psychiatry”. 47. 11, s. 1244-6, 1985. PMID: 6389776. 
  • Tschampa HJ, Zerr I, Urbach H. Radiological assessment of Creutzfeldt-Jakob disease.. „Eur Radiol”. 17. 5, s. 1200-11, 2007. DOI: 10.1007/s00330-006-0456-2. PMID: 17093966. 
  • Budka H, Aguzzi A, Brown P, Brucher JM, Bugiani O, Gullotta F, Haltia M, Hauw JJ, Ironside JW, Jellinger K. Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human spongiform encephalopathies (prion diseases). „Brain Pathol”. 5. 4, s. 459-66, 1997. PMID: 8974629. 
  • Will RG, Zeidler M, Stewart GE, Macleod MA, Ironside JW, Cousens SN, Mackenzie J, Estibeiro K, Green AJ, Knight RS. Diagnosis of new variant Creutzfeldt-Jakob disease. „Ann Neurol”. 47. 5, s. 575-82, 2000. PMID: 10805327. 

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