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Kouri-Kapsampeli Ε, Politis Τ, Vorou-Papavassiliou R:
"The human transmissible spongiform encephalopathies (tse) implications in dentistry. a recent review of the literature ",
STOMATOLOGIA 61 (4) : 183-187 (Dec 2004)


References included in article: 27 records found.

Order of appearence Full citation SRCosmos Link 
1Porter S, Scully C, Ridgway GL, Bell J,
2000. The human transmissible spongiform encephalopathies (TSEs): implications for dental practicioners. Br Dent J, 188: 432-436
 
2Daljit GS, Tredwin CJ, Gill SK,
2001. The transmissible spongiform encephalopathies (prion disease): a review for dental surgeons. Int Dent J, 51: 439-446
 
3Chan SWY, Collins S, Masters CL, Walker DM,
2001. Classical and variant Creutzfeldt-Jakob diseases and their potential impact of the practice of clinical dentistry in Australia. Aus Dent J, 46: 251-257
 
4Bagg J, Sweeney CP, Roy KM, Sharp T, Smith A,
2001. Cross infection control measures and the treatment of patients at risk of Creutzfeldt-Jakob disease in UK general dental practice. Br Dent J, 191: 87-90
 
5Gonzales TS, Rushing EJ,
1998. Bad and good news: what the dentist needs to know about transmissible spongiform encephalopathies. Quintessence Int, 29: 319-321
 
6Prusiner SB,
1993. Prion encephalopathies of animals and humans. Dev Biol Stand, 80: 31-44
 
7Goldman W,
1993. PrP gene and its association with spongiform encephalopathies. Br Med Bull, 49: 839-859
 
8Mertz PA,
SOMERVILLE RA, WISNIEWSKI H.M., MANUELIDIS L, MANUELIDIS E.E., 1983. Scarpieassociated fibrils in Creutzfeldt-Jakob disease. Nature, 306: 474-476
 
9Taylor DM,
1991. Inactivation of the unconventional agents of scarpic, bone spongiform encephalopathy and Creutzfeldt-Jakob disease. J Hosp Infect, 18: 141-146
 
10Cousens SN, Zeidler M, Esmonde TF,
De -ILVA R., WILESMITH J.W., SMITH P.G. et al., 1997. Sporadic Creutzfeldt-Jakob disease in UK: analysis of epidemiological surveillance data for 1970-1996. µr Med J, 315: 389-396
 
11Collinge J, Palmer MS,
1997. Prion Diseases. Oxford University Press, Oxford: 30-32
 
12Lantos PL,
1992. From slow virus to prion protein: a review of transmissible spongiform encephalopathies. Histopathology, 20: 1-11
 
13Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN,
et al. 1990. Prion dementia without characteristic pathology. Lancet, 336: 7-9
 
14Brown P, Gibbs CJ, Rodgers-Johnson P,
et al., 1994. Human spongiform encephalopathy: the national institutes of health series of 300 cases of experimentally transmitted disease. An Neurol, 35: 5l3-529
 
15Bernoulli C, Siegfried J, Baumgartner G,
et al., 1977. Danger of accidental person-to-person transmission of Greutzfeldt-Jakob disease by surgery. Lancet, 1: 478-479
 
16Masters CL, Harris JO, Gajdusek DC,
et al., 1978. Creutzfeldt-Jakob disease: patterns of worldwide occurrence and the significance of familial and sporadic clustering. Αnn Neurol, 5: 177-188
 
17Cousens SN, Linsell L, Smith PG, Chandrakumar M, Wilesmith JW,
et al., 1999. Geographical distribution of variant GJD in the UK. Lancet, 353: 18-21
 
18Will RG, Ironside JW, Zeidler M, Cousens SN, Estibeiro K, Alperovitch A,
et al., 1996. A new Σariant of Creutzfeldt-Jakob disease in the UK. Lancet, 347: 921-925
 
19Deslys JP, Lasmezas CI, Streichenberger N, Hilla A, Collinge J, Dormont D,
et al., 1997. New variant Creutzfeldt-Jakob disease in France. Lancet, 349: 30-31
 
20Zeidler M,
JOHNSTONE EC, BAMBER RW et al. 1997. New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet, 350: 908-910
 
21Hill AF, Butterworth RJ, Joiner S, Jackson G, Rossor MN, Thomas DJ,
et al., 1999. Investigation Τf variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples. Lancet, 353: 183-189
 
22Zeidler M, Johnstone EC, Bamber RW, Dickens CM, Fischer CJ, Francis AF,
et al., 1997. New variant Creutzfeldt-Jakob disease: psychiatric features. Lancet, 350: 908-910
 
23Prusiner SB,
1998. The prion diseases. Brain Pathol 8: 499-513
 
24Weber T, Aguzzi A,
1997. The spectrum of transmissible spongiform encephalopathies. Intervirology, 40: 198-212
 
25Patterson WJ, Painter MJ,
1999. Bovine spongiform encephalopathy and new variant Creutzfeldt-Jakob disease: an overview. Commun Dis Publ Health, 2: 5-13
 
26Porter RP,
2002. Prions and dentistry. J R Soc Med, 95: 178-181
 
27WORLD HEALTH ORGANISATION. 1999. WHO Infection Control Quidelines for Transmissible Spongiform Encephalopathies. Report of a WHO Consultation. Geneva, WHO: 1-35