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Number of items: 6.

Stahl, S; Gaetzner, S; Voss, K; Brackertz, B; Schleider, E; Sürücü, O; Kunze, E; Netzer, C; Korenke, C; Finckh, U; Habek, M; Poljakovic, Z; Elbracht, M; Rudnik-Schöneborn, S; Bertalanffy, H; Sure, U; Felbor, U (2008). Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex. Human Mutation, 29(5):709-717.

Finckh, U; Hock, C; Nitsch, R M (2004). Die Alzheimer-Krankheit: Molekulare Grundlagen und Therapieansätzte. In: Ganten, D; Ruckpaul, K; Ruiz-Torres, A. Molekularmedizinische Grundlagen von altersspezifischen Erkrankungen. Heidelberg: Springer Verlag, 148-179.

Günther, C; von Hadeln, K; Müller-Thomsen, T; Alberici, A; Binetti, G; Hock, C; Nitsch, R M; Stoppe, G; Reiss, J; Gal, A; Finckh, U (2004). Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease. Neuroscience Letters, 369(3):219-223.

Benussi, L; Ghidoni, R; Steinhoff, T; Alberici, A; Villa, A; Mazzoli, F; Nicosia, F; Barbiero, L; Broglio, L; Feudatari, E; Signorini, S; Finckh, U; Nitsch, R M; Binetti, G (2003). Alzheimer disease-associated cystatin C variant undergoes impaired secretion. Neurobiology of Disease, 13(1):15-21.

Finckh, U; van Hadeln, K; Müller-Thomsen, T; Alberici, A; Binetti, G; Hock, C; Nitsch, R M; Stoppe, G; Reiss, J; Gal, A (2003). Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2. Neurogenetics, 4(4):213-217.

Finckh, U; Müller-Thomsen, T; Mann, U; Eggers, C; Marksteiner, J; Meins, W; Binetti, G; Alberici, A; Sonderegger, P; Hock, C; Nitsch, R M; Gal, A (2000). High frequency of mutations in four different disease genes in early-onset dementia. Annals of the New York Academy of Sciences, 920:100-106.

This list was generated on Wed Jul 26 13:11:17 2017 CEST.