307 related articles for article (PubMed ID: 11810193)
21. Localization of disease-related PrP in Danish patients with different subtypes of prion disease.
Bergström AL; Heegaard PM; Dyrbye H; Lind P; Laursen H
Clin Neuropathol; 2009; 28(5):321-32. PubMed ID: 19788047
[TBL] [Abstract][Full Text] [Related]
22. Quantification of surviving cerebellar granule neurones and abnormal prion protein (PrPSc) deposition in sporadic Creutzfeldt-Jakob disease supports a pathogenic role for small PrPSc deposits common to the various molecular subtypes.
Faucheux BA; Morain E; Diouron V; Brandel JP; Salomon D; Sazdovitch V; Privat N; Laplanche JL; Hauw JJ; Haïk S
Neuropathol Appl Neurobiol; 2011 Aug; 37(5):500-12. PubMed ID: 21450052
[TBL] [Abstract][Full Text] [Related]
23. Cerebrovascular P-glycoprotein expression is decreased in Creutzfeldt-Jakob disease.
Vogelgesang S; Glatzel M; Walker LC; Kroemer HK; Aguzzi A; Warzok RW
Acta Neuropathol; 2006 May; 111(5):436-43. PubMed ID: 16523342
[TBL] [Abstract][Full Text] [Related]
24. Towards authentic transgenic mouse models of heritable PrP prion diseases.
Watts JC; Giles K; Bourkas ME; Patel S; Oehler A; Gavidia M; Bhardwaj S; Lee J; Prusiner SB
Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
[TBL] [Abstract][Full Text] [Related]
25. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.
Collins S; McLean CA; Masters CL
J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002
[TBL] [Abstract][Full Text] [Related]
26. Neuroinflammation and common mechanism in Alzheimer's disease and prion amyloidosis: amyloid-associated proteins, neuroinflammation and neurofibrillary degeneration.
Rozemuller AJ; Jansen C; Carrano A; van Haastert ES; Hondius D; van der Vies SM; Hoozemans JJ
Neurodegener Dis; 2012; 10(1-4):301-4. PubMed ID: 22398730
[TBL] [Abstract][Full Text] [Related]
27. Two-dimensional mapping of three phenotype-associated isoforms of the prion protein in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Righetti PG; Ferrari S; Terrin L; Farinazzo A; Cardone F; Pocchiari M; Rizzuto N; Monaco S
Electrophoresis; 2002 Jan; 23(2):347-55. PubMed ID: 11840543
[TBL] [Abstract][Full Text] [Related]
28. Disease associated prion protein may deposit in the peripheral nervous system in human transmissible spongiform encephalopathies.
Hainfellner JA; Budka H
Acta Neuropathol; 1999 Nov; 98(5):458-60. PubMed ID: 10541867
[TBL] [Abstract][Full Text] [Related]
29. 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
[TBL] [Abstract][Full Text] [Related]
30. Different prion conformers target the olfactory pathway in sporadic Creutzfeldt-Jakob disease.
Zanusso G; Ferrari S; Benedetti D; Sbriccoli M; Rizzuto N; Monaco S
Ann N Y Acad Sci; 2009 Jul; 1170():637-43. PubMed ID: 19686205
[TBL] [Abstract][Full Text] [Related]
31. Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies.
Tateishi J; Kitamoto T; Hashiguchi H; Shii H
Ann Neurol; 1988 Jul; 24(1):35-40. PubMed ID: 3046469
[TBL] [Abstract][Full Text] [Related]
32. Curcumin binds to the alpha-helical intermediate and to the amyloid form of prion protein - a new mechanism for the inhibition of PrP(Sc) accumulation.
Hafner-Bratkovic I; Gaspersic J; Smid LM; Bresjanac M; Jerala R
J Neurochem; 2008 Mar; 104(6):1553-64. PubMed ID: 17996023
[TBL] [Abstract][Full Text] [Related]
33. Games played by rogue proteins in prion disorders and Alzheimer's disease.
Aguzzi A; Haass C
Science; 2003 Oct; 302(5646):814-8. PubMed ID: 14593165
[TBL] [Abstract][Full Text] [Related]
34. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part I].
Zaborowski A
Psychiatr Pol; 2004; 38(2):283-96. PubMed ID: 15307293
[TBL] [Abstract][Full Text] [Related]
35. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
Sikorska B; Liberski PP; Sobów T; Budka H; Ironside JW
Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
[TBL] [Abstract][Full Text] [Related]
36. Classification of sporadic Creutzfeldt-Jakob disease revisited.
Cali I; Castellani R; Yuan J; Al-Shekhlee A; Cohen ML; Xiao X; Moleres FJ; Parchi P; Zou WQ; Gambetti P
Brain; 2006 Sep; 129(Pt 9):2266-77. PubMed ID: 16923954
[TBL] [Abstract][Full Text] [Related]
37. A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation.
Miyazono M; Iwaki T; Kitamoto T; Kaneko Y; Doh-ura K; Tateishi J
Am J Pathol; 1991 Sep; 139(3):589-98. PubMed ID: 1679596
[TBL] [Abstract][Full Text] [Related]
38. UV light-induced autofluorescence of full-length Abeta-protein deposits in the human brain.
Thal DR; Ghebremedhin E; Haass C; Schultz C
Clin Neuropathol; 2002; 21(1):35-40. PubMed ID: 11846043
[TBL] [Abstract][Full Text] [Related]
39. Increased expression of water channel aquaporin 1 and aquaporin 4 in Creutzfeldt-Jakob disease and in bovine spongiform encephalopathy-infected bovine-PrP transgenic mice.
Rodríguez A; Pérez-Gracia E; Espinosa JC; Pumarola M; Torres JM; Ferrer I
Acta Neuropathol; 2006 Nov; 112(5):573-85. PubMed ID: 16871401
[TBL] [Abstract][Full Text] [Related]
40. Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease.
Kitamoto T; Tateishi J; Sato Y
Ann Neurol; 1988 Oct; 24(4):537-42. PubMed ID: 3071243
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
