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Results:
1-12
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Results: 12
Authors:
Oehmichen, M
Schulz-Schaffer, W
Kretzschmar, H
Theuerkauf, I
Gerling, I
Windl, O
Meissner, C
Citation: M. Oehmichen et al., Creutzfeldt-Jakob disease (CJD) in a case of suspected chronic heavy metalpoisoning, J FOREN SCI, 46(3), 2001, pp. 702-707
Authors:
Kramer, ML
Kratzin, HD
Schmidt, B
Romer, A
Windl, O
Liemann, S
Hornemann, S
Kretzschmar, H
Citation: Ml. Kramer et al., Prion protein binds copper within the physiological concentration range, J BIOL CHEM, 276(20), 2001, pp. 16711-16719
Authors:
Zerr, I
Schulz-Schaeffer, WJ
Giese, A
Bodemer, M
Schroter, A
Henkel, K
Tschampa, HJ
Windl, O
Pfahlberg, A
Steinhoff, BJ
Gefeller, O
Kretzschmar, HA
Poser, S
Citation: I. Zerr et al., Current clinical diagnosis in Creutzfeldt-Jakob disease: Identification ofuncommon variants, ANN NEUROL, 48(3), 2000, pp. 323-329
Authors:
Otto, M
Esselmann, H
Schulz-Schaeffer, W
Neumann, M
Schroter, A
Ratzka, P
Cepek, L
Zerr, I
Steinacker, P
Windl, O
Kornhuber, J
Kretzschmar, HA
Poser, S
Wiltfang, J
Citation: M. Otto et al., Decreased beta-amyloid(1-42) in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease, NEUROLOGY, 54(5), 2000, pp. 1099-1102
Authors:
Skworc, KH
Windl, O
Schulz-Schaeffer, WJ
Giese, A
Bergk, J
Nagele, A
Vieregge, P
Zerr, I
Poser, S
Kretzschmar, HA
Citation: Kh. Skworc et al., Familial Creutzfeldt-Jakob disease with a novel 120-bp insertion in the prion protein gene, ANN NEUROL, 46(5), 1999, pp. 693-700
Authors:
Parchi, P
Giese, A
Capellari, S
Brown, P
Schulz-Schaeffer, W
Windl, O
Zerr, I
Budka, H
Kopp, N
Piccardo, P
Poser, S
Rojiani, A
Streichemberger, N
Julien, J
Vital, C
Ghetti, B
Gambetti, P
Kretzschmar, H
Citation: P. Parchi et al., Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects, ANN NEUROL, 46(2), 1999, pp. 224-233
Authors:
Windl, O
Giese, A
Schulz-Schaeffer, W
Zerr, I
Skworc, K
Arendt, S
Oberdieck, C
Bodemer, M
Poser, S
Kretzschmar, HA
Citation: O. Windl et al., Molecular genetics of human prion diseases in Germany, HUM GENET, 105(3), 1999, pp. 244-252
Authors:
Herms, J
Tings, T
Gall, S
Madlung, A
Giese, A
Siebert, H
Schurmann, P
Windl, O
Brose, N
Kretzschmar, H
Citation: J. Herms et al., Evidence of presynaptic location and function of the prion protein, J NEUROSC, 19(20), 1999, pp. 8866-8875
Authors:
Harder, A
Jendroska, K
Kreuz, F
Wirth, T
Schafranka, C
Karnatz, N
Theallier-Janko, A
Kreier, J
Lohan, K
Emmerich, D
Cervos-Navarro, J
Windl, O
Kretzschmar, HA
Nurnberg, P
Witkowski, R
Citation: A. Harder et al., Novel twelve-generation kindred of fatal familial insomnia from Germany representing the entire spectrum of disease expression, AM J MED G, 87(4), 1999, pp. 311-316
Authors:
Windl, O
Lorenz, H
Behrens, C
Romer, A
Kretzschmar, HA
Citation: O. Windl et al., Construction and characterization of murine neuroblastoma cell clones allowing inducible and high expression of the prion protein, J GEN VIROL, 80, 1999, pp. 15-21
Authors:
Almer, G
Hainfellner, JA
Brucke, T
Jellinger, K
Kleinert, R
Bayer, G
Windl, O
Kretzschmar, HA
Hill, A
Sidle, K
Collinge, J
Budka, H
Citation: G. Almer et al., Fatal familial insomnia: a new Austrian family, BRAIN, 122, 1999, pp. 5-16
Authors:
Kropp, S
Schulz-Schaeffer, WJ
Finkenstaedt, M
Riedemann, C
Windl, O
Steinhoff, BJ
Zerr, I
Kretzschmar, HA
Poser, S
Citation: S. Kropp et al., The Heidenhain variant of Creutzfeldt-Jakob disease, ARCH NEUROL, 56(1), 1999, pp. 55-61
Risultati:
1-12
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