References

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References

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Belay ED, Schonberger LB. The public health impact of prion diseases. Annu Rev Pub Hlth. 2005; 26:191. Available at: https://www.cdc.gov/prions/pdfs/public-health-impact.pdf. Accessed April 29, 2020.
Brown P, Brunk C, Budka H, Cervenakova L, Collie D, et al. WHO manual for surveillance of human transmissible spongiform encephalopathies including variant Creutzfeldt-Jakob disease, World Health Organization, Geneva, Switzerland; 2003. Available at: http://whqlibdoc.who.int/publications/2003/9241545887.pdf. Accessed April 29, 2020.
Collins S, McLean CA, Masters CL. Gerstmann-Sträussler-Scheinker syndrome, fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies. J Clin Neuro. 2001; 8(5):387.
Johnson RT. Prion diseases. Lancet Neurol. 2005; 4:635.
Kovacs GG, Budka H. Molecular Pathology of Human Prion Diseases. Int J Mol Sci. 2009; 10:976. Available at:http://www.mdpi.com/1422-0067/10/3/976. Accessed April 29, 2020.
McKintosh E, Tabrizi SJ, Collinge J. Prion diseases. J Neuro Virol. 2003; 9:183. Available at:http://www.jneurovirol.com/o_pdf/9(2)/183-193.pdf. Accessed April 29, 2020.
Soundarya S, Usha V, Bhuvaneshwari S. Prion diseases of human: A review. Inter J Oral and Maxillofacial Path. 2013; 4(1):43.
World Health Organization. Infection Control Guidelines for Transmissible Spongiform Encephalopathies. WHO, Geneva, Switzerland; 1999. Available at:http://www.who.int/csr/resources/publications/bse/whocdscsraph2003.pdf. Accessed April 29, 2020.
World Health Organization. Understanding the BSE Threat. WHO, Geneva, Switzerland; 2002. Available at:http://whqlibdoc.who.int/hq/2002/WHO_CDS_CSR_EPH_2002.6.pdf?ua=1. Accessed April 29, 2020.