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Results 1 to 25 of 72

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Implications of prion diseases for neurosurgery. CommentaryBLÄTTLER, Thomas; SIEGEL, Adrian M.Neurosurgical review. 2002, Vol 25, Num 4, pp 195-204, issn 0344-5607, 10 p.Article

The allograft inflammatory factor-1 in Creutzfeldt-Jakob disease brainsDEININGER, M. H; WEINSCHENK, T; MEYERMANN, R et al.Neuropathology and applied neurobiology (Print). 2003, Vol 29, Num 4, pp 389-399, issn 0305-1846, 11 p.Article

Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathiesPOCCHIARI, M; PUOPOLO, M; BRANDEL, J.-P et al.Brain. 2004, Vol 127, pp 2348-2359, issn 0006-8950, 12 p., 10Article

Soil-mediated prion transmission: Is local soil-type a key determinant of prion disease incidence?SAUNDERS, Samuel E; BARTZ, Jason C; BARTELT-HUNT, Shannon L et al.Chemosphere (Oxford). 2012, Vol 87, Num 7, pp 661-667, issn 0045-6535, 7 p.Article

De la formation à l'autoformation: le «forme-toi toi-même» du CJD = From training to self-training: the CJD's method teach yourselfGRANDJEAN, H.Education permanente. 1993, Num 114, pp 169-174, issn 0339-7513Article

Prion disease geneticsMEAD, Simon.European journal of human genetics. 2006, Vol 14, Num 3, pp 273-281, issn 1018-4813, 9 p.Article

Variant CJD: the present position and future possibilitiesKNIGHT, Richard.International journal of pediatric otorhinolaryngology. 2003, Vol 67, pp S81-S84, issn 0165-5876, SUP1Conference Paper

Correlating DWI MRI With Pathologic and Other Features of Jakob-Creutzfeldt DiseaseGESCHWIND, Michael D; POTTER, Christopher A; SATTAVAT, Mamta et al.Alzheimer disease and associated disorders. 2009, Vol 23, Num 1, pp 82-87, issn 0893-0341, 6 p.Article

Molecular subtype-specific clinical diagnosis of prion diseasesHEINEMANN, Uta; KRASNIANSKI, Anna; MEISSNER, Bettina et al.Veterinary microbiology (Amsterdam). 2007, Vol 123, Num 4, pp 328-335, issn 0378-1135, 8 p.Conference Paper

Current limitations about the cleaning of luminal endoscopesHERVE, R; KEEVIL, C. W.The Journal of hospital infection. 2013, Vol 83, Num 1, pp 22-29, issn 0195-6701, 8 p.Article

An immunoassay for the pathological form of the prion protein based on denaturation and time resolved fluorometryDABAGHIAN, Reza H; BARNARD, Geoff; MCCONNELL, Ian et al.Journal of virological methods. 2006, Vol 132, Num 1-2, pp 85-91, issn 0166-0934, 7 p.Article

The role of the cellular prion protein in the immune systemISAACS, J. D; JACKSON, G. S; ALTMANN, D. M et al.Clinical and experimental immunology (Print). 2006, Vol 146, Num 1, pp 1-8, issn 0009-9104, 8 p.Article

White matter involvement in sporadic Creutzfeldt-Jakob diseaseCAVERZASI, Eduardo; MANDELLI, Maria Luisa; GESCHWIND, Michael D et al.Brain. 2014, Vol 137, pp 3339-3354, issn 0006-8950, 16 p., 12Article

Sporadic Creutzfeldt-Jakob disease: a description of two casesDAS, Kavita; DAVIS, Rebecca; DUTOIT, Brett et al.International psychogeriatrics. 2012, Vol 24, Num 7, pp 1183-1185, issn 1041-6102, 3 p.Article

The Prion DiseasesBROWN, Khalilah; MASTRIANNI, James A.Journal of geriatric psychiatry and neurology. 2010, Vol 23, Num 4, pp 277-298, issn 0891-9887, 22 p.Article

Enhanced geographically restricted surveillance simulates sporadic Creutzfeldt-Jakob disease clusterKLUG, Genevieve M; WAND, Handan; BOYD, Alison et al.Brain. 2009, Vol 132, pp 493-501, issn 0006-8950, 9 p., 2Article

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob diseaseZERR, I; KALLENBERG, K; SCHUUR, M et al.Brain. 2009, Vol 132, pp 2659-2668, issn 0006-8950, 10 p., 10Article

Creutzfeldt-Jakob disease in Germany : a prospective 12-year surveillanceHEINEMANN, U; KRASNIANSKI, A; MEISSNER, B et al.Brain. 2007, Vol 130, pp 1350-1359, issn 0006-8950, 10 p., 5Article

Patients' perception of infection prevention in dental practiceSMITH, Andrew J; WILSON, Sarah L; READ, Sarah et al.American journal of infection control. 2014, Vol 42, Num 3, pp 337-339, issn 0196-6553, 3 p.Article

Analysis of PRNP gene codon 129 polymorphism in the greek populationSAETTA, Angelica A; M ICHALOPOULOS, Nikolaos V; MALAMIS, George et al.European journal of epidemiology. 2006, Vol 21, Num 3, pp 211-215, issn 0393-2990, 5 p.Article

Rapid method for the sensitive detection of protein contamination on surgical instrumentsLIPSCOMB, I. P; SIHOTA, A. K; BOTHAM, M et al.The Journal of hospital infection. 2006, Vol 62, Num 2, pp 141-148, issn 0195-6701, 8 p.Article

Regional brain metabolite abnormalities in inherited prion disease and asymptomatic gene carriers demonstrated in vivo by quantitative proton magnetic resonance spectroscopyWALDMAN, A. D; CORDERY, R. J; MACMANUS, D. G et al.Neuroradiology (Berlin. Print). 2006, Vol 48, Num 6, pp 428-433, issn 0028-3940, 6 p.Article

Plasminogen activities and concentrations in patients with sporadic Creutzfeldt-Jakob diseaseZERR, Inga; BODEMER, Monika; KABOTH, Ulrich et al.Neuroscience letters. 2004, Vol 371, Num 2-3, pp 163-166, issn 0304-3940, 4 p.Article

Prion protein polymerisation triggered by manganese-generated prion protein seedsHESKETH, Shirley; THOMPSETT, Andrew R; BROWN, David R et al.Journal of neurochemistry. 2012, Vol 120, Num 1-2, pp 177-189, issn 0022-3042, 13 p.Article

Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob diseaseSATOH, Katsuya; TOBIUME, Minoru; MATSUI, Yuki et al.Laboratory investigation. 2010, Vol 90, Num 11, pp 1637-1644, issn 0023-6837, 8 p.Article

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