Reviews And Selected Updates

Brown P, Cathala F, Raubertas RF, et al: The epidemiology of Creutzfeldt- Jakob disease: Conclusion of a 15-year investigation in France and review of the world literature. Neurology 1987;37:895-904.

Brown P: A therapeutic panorama of the spongiform encephalopathies. Antiviral Chem Chemother 1990;1:75-83.

Brown P: Transmissible human spongiform encephalopathy (infectious cerebral amyloidosis): Creutzfeldt-Jakob disease, Gerstmann-Straussler- Scheinker syndrome, and kuru. In Calne D (ed): Neurodegenerative Diseases. Philadelphia, WB Saunders, 1994, pp 839-876.

Finkenstaedt M, Szudra A, Zerr I, et al: MR imaging of Creutzfeldt- Jakob disease. Radiology 1996;199:793-798.

Gajdusek DC: Infectious and noninfectious amyloidoses of the brain: Systemic amyloidoses as predictive models in transmissible and nontransmissible amyloidotic neurodegeneration of Creutzfeldt-Jakob disease and aging brain and Alzheimer's disease. In Calne DB (ed): Neurodegenerative Diseases. Philadelphia, Wb Saunders, 1994, pp 301-317.

Gambetti P, Parchi P, Petersen RB, et al: Fatal familial insomnia and familial Creutzfeldt-Jakob disease: Clinical, pathological and molecular features. Brain Pathol 1995;5:43-51.

Prusiner SB: Prions. In Fields BM, Knipe DM, Howley PM (eds): Fields Virology. Philadelphia, Lippincott-Raven, 1996, pp 2901-2950. Will RG, Ironside JW, Zeidler M, et al: A new variant of Creutzfeldt- Jakob disease in the UK. Lancet 1996;347:921-925.

Zerr I, Bodemer M, Gefeller O, et al: Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease. Ann Neurol 1998;43:32-40.


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