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311 related items for PubMed ID: 20547859
21. Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype. Cracco L, Puoti G, Cornacchia A, Glisic K, Lee SK, Wang Z, Cohen ML, Appleby BS, Cali I. Acta Neuropathol Commun; 2023 Aug 31; 11(1):141. PubMed ID: 37653534 [Abstract] [Full Text] [Related]
22. Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation. Watts JC, Giles K, Serban A, Patel S, Oehler A, Bhardwaj S, Guan S, Greicius MD, Miller BL, DeArmond SJ, Geschwind MD, Prusiner SB. Ann Neurol; 2015 Oct 31; 78(4):540-53. PubMed ID: 26094969 [Abstract] [Full Text] [Related]
23. Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics. Cali I, Puoti G, Smucny J, Curtiss PM, Cracco L, Kitamoto T, Occhipinti R, Cohen ML, Appleby BS, Gambetti P. Sci Rep; 2020 Jan 30; 10(1):1503. PubMed ID: 32001774 [Abstract] [Full Text] [Related]
28. MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan. Fukushima R, Shiga Y, Nakamura M, Fujimori J, Kitamoto T, Yoshida Y. J Neurol Neurosurg Psychiatry; 2004 Mar 30; 75(3):485-7. PubMed ID: 14966171 [Abstract] [Full Text] [Related]
30. PrP mRNA and protein expression in brain and PrP(c) in CSF in Creutzfeldt-Jakob disease MM1 and VV2. Llorens F, Ansoleaga B, Garcia-Esparcia P, Zafar S, Grau-Rivera O, López-González I, Blanco R, Carmona M, Yagüe J, Nos C, Del Río JA, Gelpí E, Zerr I, Ferrer I. Prion; 2013 Mar 30; 7(5):383-93. PubMed ID: 24047819 [Abstract] [Full Text] [Related]
32. Absence of Evidence for a Causal Link between Bovine Spongiform Encephalopathy Strain Variant L-BSE and Known Forms of Sporadic Creutzfeldt-Jakob Disease in Human PrP Transgenic Mice. Jaumain E, Quadrio I, Herzog L, Reine F, Rezaei H, Andréoletti O, Laude H, Perret-Liaudet A, Haïk S, Béringue V. J Virol; 2016 Dec 01; 90(23):10867-10874. PubMed ID: 27681129 [Abstract] [Full Text] [Related]
33. Clinicopathologic characteristics of sporadic Japanese Creutzfeldt-Jakob disease classified according to prion protein gene polymorphism and prion protein type. Iwasaki Y, Yoshida M, Hashizume Y, Kitamoto T, Sobue G. Acta Neuropathol; 2006 Nov 01; 112(5):561-71. PubMed ID: 16847689 [Abstract] [Full Text] [Related]