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Number of items: 6.

Meissner, B; Kallenberg, K; Sanchez-Juan, P; Collie, D; Summers, D M; Almonti, S; Collins, S J; Smith, P; Cras, P; Jansen, G H; Brandel, J P; Coulthart, M B; Roberts, H; Van Everbroeck, B; Galanaud, D; Mellina, V; Will, R G; Zerr, I (2009). MRI lesion profiles in sporadic Creutzfeldt-Jakob disease. Neurology, 72(23):1994-2001.

Zerr, I; Kallenberg, K; Summers, D M; Romero, C; Taratuto, A; Heinemann, U; Breithaupt, M; Varges, D; Meissner, B; Ladogana, A; Schuur, M; Haik, S; Collins, S J; Jansen, G H; Stokin, G B; Pimentel, J; Hewer, E; Collie, D; Smith, P; Roberts, H; Brandel, J P; van Duijn, C; Pocchiari, M; Begue, C; Cras, P; Will, R G; Sanchez-Juan, P (2009). Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease. Brain: A Journal of Neurology, 132(Pt 10):2659-2668.

Krasnianski, A; Kallenberg, K; Collie, D A; Meissner, B; Schulz-Schaeffer, W J; Heinemann, U; Varges, D; Summers, D M; Kretzschmar, H A; Talbot, T; Will, R G; Zerr, I (2008). MRI in the classical MM1 and the atypical MV2 subtypes of sporadic CJD: an inter-observer agreement study. European Journal of Neurology, 15(8):762-771.

Ladogana, A; Puopolo, M; Croes, E A; Budka, H; Jarius, C; Collins, S; Klug, G M; Sutcliffe, T; Giulivi, A; Alperovitch, A; Delasnerie-Laupretre, N; Brandel, J-P; Poser, S; Kretzschmar, H A; Rietveld, I; Mitrova, E; Cuesta, J de Pedro; Martinez-Martin, P; Glatzel, M; Aguzzi, A; Knight, R; Ward, H; Pocchiari, M; van Duijn, C M; Will, R G; Zerr, I (2005). Mortality from Creutzfeldt-Jakob disease and related disorders in Europe, Australia, and Canada. Neurology, 64(9):1586-1591.

Pocchiari, M; Puopolo, M; Croes, E A; Budka, H; Gelpi, E; Collins, S; Lewis, V; Sutcliffe, T; Guilivi, A; Delasnerie-Laupretre, N; Brandel, J-P; Alperovitch, A; Zerr, I; Poser, S; Kretzschmar, H A; Ladogana, A; Rietvald, I; Mitrova, E; Martinez-Martin, P; de Pedro-Cuesta, J; Glatzel, M; Aguzzi, A; Cooper, S; Mackenzie, J; van Duijn, C M; Will, R G (2004). Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Brain: A Journal of Neurology, 127(10):2348-2359.

Budka, H; Aguzzi, A; Brown, P; Brucher, J M; Bugiani, O; Collinge, J; Diringer, H; Gullotta, F; Haltia, M; Hauw, J J; Ironside, J W; Kretzschmar, H A; Lantos, P L; Masullo, C; Pocchiari, M; Schlote, W; Tateishi, J; Will, R G (1996). [Consensus report: tissue handling in suspected Creutzfeldt-Jakob disease and other spongiform encephalopathies (prion diseases) in the human. European Union Biomed-1 Concerted Action]. Der Pathologe, 17(2):171-175.

This list was generated on Sat Oct 21 06:25:18 2017 CEST.