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Prion
Citations 21-30 of 61 total displayed.
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Past content
(since Aug 2001):
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- ARTICLES
Australian sporadic CJD analysis supports endogenous determinants of molecular-clinical profiles
- V. Lewis, A. F. Hill, G. M. Klug, A. Boyd, C. L. Masters, and S. J. Collins
Neurology 2005; 65: 113-118.
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- BRIEF COMMUNICATIONS
Evaluation of urinary PrPSc as a diagnostic test for sporadic, variant, and familial CJD
- M. W. Head, E. Kouverianou, L. Taylor, A. Green, and R. Knight
Neurology 2005; 64: 1794-1796.
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- ARTICLES
Mortality from Creutzfeldt–Jakob disease and related disorders in Europe, Australia, and Canada
- A. Ladogana, M. Puopolo, E. A. Croes, H. Budka, C. Jarius, S. Collins, G. M. Klug, T. Sutcliffe, A. Giulivi, A. Alperovitch, N. Delasnerie-Laupretre, J. -P. Brandel, S. Poser, H. Kretzschmar, I. Rietveld, E. Mitrova, J. de Pedro Cuesta, P. Martinez-Martin, M. Glatzel, A. Aguzzi, R. Knight, H. Ward, M. Pocchiari, C. M. van Duijn, R. G. Will, and I. Zerr
Neurology 2005; 64: 1586-1591.
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High incidence of genetic human transmissible spongiform encephalopathies in Italy
- A. Ladogana, M. Puopolo, A. Poleggi, S. Almonti, V. Mellina, M. Equestre, and M. Pocchiari
Neurology 2005; 64: 1592-1597.
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PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia
- D. A. Hall, M. A. Leehey, C. M. Filley, E. Steinbart, T. Montine, G. D. Schellenberg, P. Bosque, R. Nixon, and T. Bird
Neurology 2005; 64: 1304-1306.
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- ARTICLES
Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease
- T. Hamaguchi, T. Kitamoto, T. Sato, H. Mizusawa, Y. Nakamura, M. Noguchi, Y. Furukawa, C. Ishida, I. Kuji, K. Mitani, S. Murayama, T. Kohriyama, S. Katayama, M. Yamashita, T. Yamamoto, F. Udaka, A. Kawakami, Y. Ihara, T. Nishinaka, S. Kuroda, N. Suzuki, Y. Shiga, H. Arai, M. Maruyama, and M. Yamada
Neurology 2005; 64: 643-648.
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Compassionate use of quinacrine in Creutzfeldt–Jakob disease fails to show significant effects
- S. Haïk, J. P. Brandel, D. Salomon, V. Sazdovitch, N. Delasnerie-Lauprêtre, J. L. Laplanche, B. A. Faucheux, C. Soubrié, E. Boher, C. Belorgey, J. J. Hauw, and A. Alpérovitch
Neurology 2004; 63: 2413-2415.
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Dissociation in circadian rhythms in a pseudohypersomnia form of fatal familial insomnia
- Y. Dauvilliers, K. Cervena, B. Carlander, F. Espa, C. Bassetti, B. Claustrat, J. L. Laplanche, M. Billiard, and J. Touchon
Neurology 2004; 63: 2416-2418.
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- ARTICLES
A case-control study of sporadic Creutzfeldt-Jakob disease in the United Kingdom: Analysis of clustering
- L. Linsell, S. N. Cousens, P. G. Smith, R. S.G. Knight, M. Zeidler, G. Stewart, R. de Silva, T. F.G. Esmonde, H. J.T. Ward, and R. G. Will
Neurology 2004; 63: 2077-2083.
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- ARTICLES
Cortical reorganization in malformations of cortical development: A magnetoencephalographic study
- Jorge G. Burneo, Ruben I. Kuzniecky, Martina Bebin, and Robert C. Knowlton
Neurology 2004; 63: 1818-1824.
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