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Number of items: 9.

Jung, H H; Bremer, J; Streffer, J; Virdee, K; Spillantini, M G; Crowther, R A; Brugger, P; van Broekhoven, C; Aguzzi, A; Tolnay, M (2012). Phenotypic variation of autosomal-dominant corticobasal degeneration. European Neurology, 67(3):142-150.

Polymenidou, M; Prokop, S; Jung, H H; Hewer, E; Peretz, D; Moos, R; Tolnay, M; Aguzzi, A (2011). Atypical prion protein conformation in familial prion disease with PRNP P105T mutation. Brain Pathology, 21(2):209-214.

Neumann, M; Tolnay, M; Mackenzie, I R A (2009). The molecular basis of frontotemporal dementia. Expert Reviews in Molecular Medicine, 11:e23.

Baumann, F; Pahnke, J; Radovanovic, I; Rülicke, T; Bremer, J; Tolnay, M; Aguzzi, A (2009). Functionally relevant domains of the prion protein identified in vivo. PLoS ONE, 4(9):e6707.

Baumann, C R; Bassetti, C L; Valko, P O; Haybaeck, J; Keller, M; Clark, E; Stocker, R; Tolnay, M; Scammell, T E (2009). Loss of hypocretin (orexin) neurons with traumatic brain injury. Annals of Neurology, 66(4):555-559.

Poretti, Andrea; Huisman, Thierry A G M; Tolnay, M; Brehmer, U; Schmitt, B; Boltshauser, E (2008). Beteiligung der Pons bei schwerer hypoxisch-ischämischer Enzephalopathie bei Termingeborenen. Aktuelle Neuropädiatrie:257-261.

Geser, F; Tolnay, M; Jung, H H (2008). The neuropathology of McLeod syndrome. In: Walker, R; Sano, A; Danek, A. Neuroacanthocytosis Syndromes II. Berlin Heidelberg: Springer, 197-203.

Baumann, F; Tolnay, M; Brabeck, C; Pahnke, J; Kloz, U; Niemann, H H; Heikenwalder, M; Rülicke, T; Bürkle, A; Aguzzi, A (2007). Lethal recessive myelin toxicity of prion protein lacking its central domain. EMBO Journal, 26(2):538-547.

Schoch, G; Seeger, H; Bogousslavsky, J; Tolnay, M; Janzer, R C; Aguzzi, A; Glatzel, M (2006). Analysis of prion strains by PrPSc profiling in sporadic Creutzfeldt-Jakob disease. PLoS Medicine, 3(2):e14.

This list was generated on Tue Jul 25 17:06:01 2017 CEST.