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- W2085383807 abstract "European Journal of NeurologyVolume 15, Issue 5 p. 435-436 Creutzfeldt-Jakob disease: hopes for therapy M. Pocchiari, M. Pocchiari Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorA. Ladogana, A. Ladogana Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorS. Graziano, S. Graziano Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorM. Puopolo, M. Puopolo Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this author M. Pocchiari, M. Pocchiari Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorA. Ladogana, A. Ladogana Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorS. Graziano, S. Graziano Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this authorM. Puopolo, M. Puopolo Department of Cell Biology and Neurosciences, Istituto Superiore di Sanità, Roma, ItalySearch for more papers by this author First published: 03 April 2008 https://doi.org/10.1111/j.1468-1331.2008.02109.xCitations: 6Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. References 1 Al-Shahi R, Will RG, Warlow CP. Amount of research interest in rare and common neurological conditions: bibliometric study. BMJ 2001; 323: 1461– 1462. 2 Trevitt CR, Collinge J. A systematic review of prion therapeutics in experimental models. Brain 2006; 129: 2241– 2265. 3 Brown P. Drug therapy in human and experimental transmissible spongiform encephalopathy. Neurology 2002; 58: 1720– 1725. 4 Ladogana A, Casaccia P, Ingrosso L, et al. Sulphate polyanions prolong the incubation period of scrapie-infected hamsters. Journal of General Virology 1992; 73: 661– 665. 5 Doh-ura K, Ishikawa K, Murakami-Kubo I, Sasaki K, Mohri S, Race R, Iwaki T. Treatment of transmissible spongiform encephalopathy by intraventricular drug infusion in animal models. Journal of Virology 2004; 78: 4999– 5006. 6 Bone I, Belton L, Walker AS, Darbyshire J. Intraventricular pentosan polysulfate in human prion diseases: an observational study in the UK. European Journal of Neurology 2008; 15: 458– 464. 7 Parry A, Baker I, Stacey R, Wimalaratna S. Long term survival in a patient with variant Creutzfeldt-Jakob disease treated with intraventricular pentosan polysulphate. Journal of Neurology, Neurosurgery and Psychiatry 2007; 78: 733– 734. 8 Rainov NG, Tsuboi Y, Krolak-Salmon P, Vighetto A, Doh-Ura K. Experimental treatments for human transmissible spongiform encephalopathies: is there a role for pentosan polysulfate? Expert Opinion of Biological Therapy 2007; 7: 713– 726. 9 Pocchiari M, Puopolo M, Croes EA, et al. Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain 2004; 127: 2348– 2359. 10 MRC Clinical Trial Unit. Prion-1 Trial: Quinacrine for human prion disease. A partially randomised patient preference trial to evaluate the activity and safety of quinacrine in human prion disease. Available at http://www.ctu.mrc.ac.uk/studies/cjd.asp (accessed 28/01/2008). 11 Kovács GG, Puopolo M, Ladogana A, et al. Genetic prion disease: the EUROCJD experience. Human Genetics 2005; 118: 166– 174. 12 Kocisko DA, Caughey B, Morrey JD, Race RE. Enhanced antiscrapie effect using combination drug treatment. Antimicrobial Agents and Chemotherapy 2006; 50: 3447– 3449. 13 Kocisko DA, Caughey B. Mefloquine, an antimalaria drug with antiprion activity in vitro, lacks activity in vivo. Journal of Virology 2006; 80: 1044– 1046. Citing Literature Volume15, Issue5May 2008Pages 435-436 ReferencesRelatedInformation" @default.
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