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Garrison-Morton-Norman History of Medicine

Prion Diseases

Exhibiting 19 entries found in the GMN corpus.

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YearTitle & TagsAuthor(s)
1996 CEA new variant of Creutzfeldt-Jakob disease in the UK.
WILL, R. G.
WILL, R. G.
IRONSIDE, J. W.
IRONSIDE, J. W.
ZEIDLER, M.
ZEIDLER, M. & et al.
2013 CEA novel prion disease associated with diarrhea and autonomic neuropathy.
MEAD, S.
MEAD, S.
GANDHI, Sonia
GANDHI, Sonia BECK, Jon
COLLINGE, John
COLLINGE, John & et al.
1965 CEAttempts to demonstrate a transmissible agent in Kuru, Amyotrophic Lateral Sclerosis, and other subacute and chronic progressive nervous system degenerations in man. Addendum p. 46 in: Slow, latent, and temperate virus infections. NINDB Monograph No. 2. Edited by D. Carleton Gajdusek, Clarence J. Gibbs, Jr., and Michael Alpers.
GAJDUSEK, Daniel Carleton (1923 – 2008)
GAJDUSEK, Daniel Carleton (1923 – 2008) GIBBS, Clarence Joseph Jr. (1924 – 2001) ALPERS, Michael
1957 CEDegenerative disease of the central nervous system in New Guinea. The endemic occurrence of “Kuru” in the native population.
GAJDUSEK, Daniel Carleton (1923 – 2008)
GAJDUSEK, Daniel Carleton (1923 – 2008) ZIGAS, Vincent (1920 – 1983)
1923 CEDie Extrapyramidalen Erkrankungen: Mit Besonderer Berücksichtigung der pathologischen Anatomie und Histologie und der Pathophysiologie der Bewegungsstörungen.
JAKOB, Afons Maria (1884 – 1931)
1967 CEDoes the agent of scrapie replicate without nucleic acids?
ALPER, Tikvah (1909 – 1995)
ALPER, Tikvah (1909 – 1995)
CRAMP, W. A.
CRAMP, W. A.
HAIG, D. A.
HAIG, D. A. & et al.
1996 CEEvidence for the conformation of the pathologic isoform of the prion protein enciphering and propagating prion diversity.
PRUSINER, Stanley Benjamin (1942 – )
PRUSINER, Stanley Benjamin (1942 – ) TELLING, Glenn C. PARCHI, Piero (1951 – ) DE ARMOND, Stephen J. & et al.
1986 CEFatal familial insomnia and dysautonomia with selective degeneration of thalamic nuclei.
LUGARESI, Elio (1926 – 2015) MEDORI, Rosella GAMBETTI, Pierluigi & et al.
1982 CEIdentification of a protein that purifies with the Scrapie prion.
PRUSINER, Stanley Benjamin (1942 – )
PRUSINER, Stanley Benjamin (1942 – ) BOLTON, David C.
MCKINLEY, Michael P.
MCKINLEY, Michael P.
1968 CEKuru and cannibalism.
MATTHEWS, John D.
MATTHEWS, John D. GLASSE, Robert M. (1930 – 1993) LINDENBAUM, Shirley
2014 CEMadness and memory: The discovery of prions- a new biological principle of disease.
PRUSINER, Stanley Benjamin (1942 – )
PRUSINER, Stanley Benjamin (1942 – )
1982 CENovel proteinaceous infectious particles cause Scrapie.
PRUSINER, Stanley Benjamin (1942 – )
PRUSINER, Stanley Benjamin (1942 – )
1959 CEScrapie and Kuru.
HADLOW, W. J.
HADLOW, W. J.
1967 CESelf replication and scrapie.
GRIFFITH, John Stanley (1928 – 1972)
GRIFFITH, John Stanley (1928 – 1972)
2004 CESynthetic mammalian prions.
PRUSINER, Stanley Benjamin (1942 – )
PRUSINER, Stanley Benjamin (1942 – ) LEGNAME, Giuseppe BASKAKOV, Ilia V. NGUYEN, Hoang-Oanh B. & et al.
1982 CEThe spectrum of Creutzfeldt-Jakob disease and the virus-induced subacute spongiform encephalopathies. IN: Smith & Cavanagh, editors, Recent advances in neuropathology, Vol. 2., Chapter 6, pp. 129-163.
GAJDUSEK, Daniel Carleton (1923 – 2008)
GAJDUSEK, Daniel Carleton (1923 – 2008) MASTERS, Colin Louis (1947 – )
1971 CETransmission of two subacute spongiform encephalopathies of man (Kuru and Creutzfeldt–Jakob disease) to New World monkeys.
GAJDUSEK, Daniel Carleton (1923 – 2008)
GAJDUSEK, Daniel Carleton (1923 – 2008) GIBBS, Clarence Joseph Jr. (1924 – 2001)
1921 CEUeber eigenartige Erkrankungen der Zentralnervensystems mit bemerkenswertem anatomischem Befunde. (Spastische Pseudosklerose — Encephalomyclopathie mit disseminirrten Degenerationsherden.)
JAKOB, Afons Maria (1884 – 1931)
1920 CEUeber eine eigenartige herdförmige Erkrankung des Zentralnervensystems.
CREUTZFELD, Hans Gerhard (1885 – 1964)