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Dietl, T; Zentner, J; Ramantani, G; Schulze-Bonhage, A; Hethey, S; Kruse, B; Reutlinger, C; Mayer, H; Steinhoff, B J; Bast, T (2016). Erfolgreiche Resektion einer fokalen kortikalen Dysplasie (FCD) der Zentralregion bei einem 6 Monate alten Säugling mit nur sehr milder postoperativer Parese. Zeitschrift für Epileptologie, 29(3):161-167.

Budka, Herbert; Kallenberg, K; Steinhoff, B J; Sturzenegger, M; Urbach, H; Weber, J R; Zerr, I (2012). Creutzfeldt-Jakob-Krankheit. In: Diener, H C; Weimar, C. Leitlinien für Diagnostik und Therapie in der Neurologie. Stuttgart: Thieme, 570-576.

Kasperaviciūte, D; Catarino, C B; Heinzen, E L; Depondt, C; Cavalleri, G L; Caboclo, L O; Tate, S K; Jamnadas-Khoda, J; Chinthapalli, K; Clayton, L M S; Shianna, K V; Radtke, R A; Mikati, M A; Gallentine, W B; Husain, A M; Alhusaini, S; Leppert, D; Middleton, L T; Gibson, R A; Johnson, M R; Matthews, P M; Hosford, D; Heuser, K; Amos, L; Ortega, M; Zumsteg, D; Wieser, H G; Steinhoff, B J; Krämer, G; Hansen, J; Dorn, T; Kantanen, A M; Gjerstad, L; Peuralinna, T; Hernandez, D G; Eriksson, K J; Kälviäinen, R K; Doherty, C P; Wood, N W; Pandolfo, M; Duncan, J S; Sander, J W; Delanty, N; Goldstein, D B; Sisodiya, S M (2010). Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Brain: A Journal of Neurology, 133(Pt 7):2136-2147.

Heinzen, E L; Radtke, R A; Urban, T J; Cavalleri, G L; Depondt, C; Need, A C; Walley, N M; Nicoletti, P; Ge, D; Catarino, C B; Duncan, J S; Kasperaviciūte, D; Tate, S K; Caboclo, L O; Sander, J W; Clayton, L; Linney, K N; Shianna, K V; Gumbs, C E; Smith, J; Cronin, K D; Maia, J M; Doherty, C P; Pandolfo, M; Leppert, D; Middleton, L T; Gibson, R A; Johnson, M R; Matthews, P M; Hosford, D; Kälviäinen, R; Eriksson, K; Kantanen, A M; Dorn, T; Hansen, J; Krämer, G; Steinhoff, B J; Wieser, H G; Zumsteg, D; Ortega, M; Wood, N W; Huxley-Jones, J; Mikati, M; Gallentine, W B; Husain, A M; Buckley, P G; Stallings, R L; Podgoreanu, M V; Delanty, N; Sisodiya, S M; Goldstein, D B (2010). Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. American Journal of Human Genetics, 86(5):707-718.

This list was generated on Thu Jul 27 06:24:40 2017 CEST.