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Results: 1-25 | 26-45 |
Results: 26-45/45

Authors: Herms, JW Korte, S Gall, S Schneider, I Dunker, S Kretzschmar, HA
Citation: Jw. Herms et al., Altered intracellular calcium homeostasis in cerebellar granule cells of prion protein-deficient mice, J NEUROCHEM, 75(4), 2000, pp. 1487-1492

Authors: Qin, KF Yang, DS Yang, Y Chishti, MA Meng, LJ Kretzschmar, HA Yip, CM Fraser, PE Westaway, D
Citation: Kf. Qin et al., Copper(II)-induced conformational changes and protease resistance in recombinant and cellular PrP - Effect of protein age and deamidation, J BIOL CHEM, 275(25), 2000, pp. 19121-19131

Authors: Herms, J Neidt, I Luscher, B Sommer, A Schurmann, P Schroder, T Bergmann, M Wilken, B Probst-Cousin, S Hernaiz-Driever, P Behnke, J Hanefeld, F Pietsch, T Kretzschmar, HA
Citation: J. Herms et al., c-myc expression in medulloblastoma and its prognostic value, INT J CANC, 89(5), 2000, pp. 395-402

Authors: Durig, J Giese, A Schulz-Schaeffer, W Rosenthal, C Schmucker, U Bieschke, J Duhrsen, U Kretzschmar, HA
Citation: J. Durig et al., Differential constitutive and activation-dependent expression of prion protein in human peripheral blood leucocytes, BR J HAEM, 108(3), 2000, pp. 488-496

Authors: Schulz-Schaeffer, WJ Tschoke, S Kranefuss, N Drose, W Hause-Reitner, D Giese, A Groschup, MH Kretzschmar, HA
Citation: Wj. Schulz-schaeffer et al., The paraffin-embedded tissue blot detects PrPSC early in the incubation time in prion diseases, AM J PATH, 156(1), 2000, pp. 51-56

Authors: Neumann, M Adler, S Schluter, O Kremmer, E Benecke, R Kretzschmar, HA
Citation: M. Neumann et al., alpha-Synuclein accumulation in a case of neurodegeneration with brain iron accumulation type 1 (NBIA-1, formerly Hallervorden-Spatz syndrome) with widespread cortical and brainstem-type Lewy bodies, ACT NEUROP, 100(5), 2000, pp. 568-574

Authors: Bleich, S Kropp, S Degner, D Zerr, I Pilz, J Gleiter, CH Otto, M Ruther, E Kretzschmar, HA Wiltfang, J Kornhuber, J Poser, S
Citation: S. Bleich et al., Creutzfeldt-Jakob disease and oxidative stress, ACT NEUR SC, 101(5), 2000, pp. 332-334

Authors: Kretzschmar, HA
Citation: Ha. Kretzschmar, Molecular pathogenesis of prion diseases, EUR ARCH PS, 249, 1999, pp. 56-63

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: 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: Kropp, S Zerr, I Schulz-Schaeffer, WJ Riedemann, C Bodemer, M Laske, C Kretzschmar, HA Poser, S
Citation: S. Kropp et al., Increase of neuron-specific enolase in patients with Creutzfeldt-Jakob disease, NEUROSCI L, 261(1-2), 1999, pp. 124-126

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: Herms, JW von Loewenich, FD Behnke, J Markakis, E Kretzschmar, HA
Citation: Jw. Herms et al., C-myc oncogene family expression in glioblastoma and survival, SURG NEUROL, 51(5), 1999, pp. 536-542

Authors: Samman, I Schulz-Schaeffer, WJ Wohrle, JC Sommer, A Kretzschmar, HA Hennerici, M
Citation: I. Samman et al., Clinical range and MRI in Creutzfeldt-Jakob disease with heterozygosity atcodon 129 and prion protein type 2, J NE NE PSY, 67(5), 1999, pp. 678-681

Authors: Wiltfang, J Otto, M Baxter, HC Bodemer, M Steinacker, P Bahn, E Zerr, I Komhuber, J Kretzschmar, HA Poser, S Ruther, E Aitken, A
Citation: J. Wiltfang et al., Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease, J NEUROCHEM, 73(6), 1999, pp. 2485-2490

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: Burkle, A Kretzschmar, HA Brown, DR
Citation: A. Burkle et al., Poly(ADP-ribose) immunostaining to detect apoptosis induced by a neurotoxic fragment of prion protein, HISTOCHEM J, 31(11), 1999, pp. 711-716

Authors: Poser, S Mollenhauer, B Krauss, A Zerr, I Steinhoff, BJ Schroeter, A Finkenstaedt, M Schulz-Schaeffer, WJ Kretzschmar, HA Felgenhauer, K
Citation: S. Poser et al., How to improve the clinical diagnosis of Creutzfeldt-Jakob disease, BRAIN, 122, 1999, pp. 2345-2351

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: 1-25 | 26-45 |