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Collins, S J; Sanchez-Juan, P; Masters, C L; Klug, G M; van Duijn, C; Poleggi, A; Pocchiari, M; Almonti, S; Cuadrado-Corrales, N; de Pedro-Cuesta, J; Budka, H; Gelpi, E; Glatzel, M; Tolnay, M; Hewer, Ekkehard; Zerr, I; Heinemann, U; Kretszchmar, H A; Jansen, G H; Olsen, E; ... (2006). Determinants of diagnostic investigation sensitivities across the clinical spectrum of sporadic Creutzfeldt-Jakob disease. Brain, 129(Pt 9), pp. 2278-2287. Oxford University Press 10.1093/brain/awl159
Ramelli, G P; Joncourt, F; Luetschg, J; Weis, J; Tolnay, M; Burgunder, J M (2006). Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss medical weekly, 136(11-12), pp. 189-93. Muttenz: EMH Schweizerischer Ärzteverlag