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Results:
1-11
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Results: 11
Authors:
Neumann, M
Schulz-Schaeffer, W
Crowther, RA
Smith, MJ
Spillantini, MG
Goedert, M
Kretzschmar, HA
Citation: M. Neumann et al., Pick's disease associated with the novel Tau gene mutation K369I, ANN NEUROL, 50(4), 2001, pp. 503-513
Authors:
Bruck, W
Herms, J
Brockmann, K
Schulz-Schaeffer, W
Hanefeld, F
Citation: W. Bruck et al., Myelinopathia centralis diffusa (vanishing white matter disease): Evidenceof apoptotic oligodendrocyte degeneration in early lesion development, ANN NEUROL, 50(4), 2001, pp. 532-536
Authors:
Tschampa, HJ
Schulz-Schaeffer, W
Wiltfang, J
Poser, S
Otto, M
Neumann, M
Kretzschmar, HA
Citation: Hj. Tschampa et al., Decreased CSF amyloid beta 42 and normal tau levels in dementia with Lewy bodies, NEUROLOGY, 56(4), 2001, pp. 576-576
Authors:
Koike, M
Nakanishi, H
Saftig, P
Ezaki, J
Isahara, K
Ohsawa, Y
Schulz-Schaeffer, W
Watanabe, T
Waguri, S
Kametaka, S
Shibata, M
Yamamoto, K
Kominami, E
Peters, C
von Figura, K
Uchiyama, Y
Citation: M. Koike et al., Cathepsin D deficiency induces lysosomal storage with ceroid lipofuscin inmouse CNS neurons, J NEUROSC, 20(18), 2000, pp. 6898-6906
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:
Bieschke, J
Giese, A
Schulz-Schaeffer, W
Zerr, I
Poser, S
Eigen, M
Kretzschmar, H
Citation: J. Bieschke et al., Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets, P NAS US, 97(10), 2000, pp. 5468-5473
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:
Kohlhase, J
Hausmann, S
Stojmenovic, G
Dixkens, C
Bink, K
Schulz-Schaeffer, W
Altmann, M
Engel, W
Citation: J. Kohlhase et al., SALL3, a New member of the human spalt-like gene family, maps to 18q23, GENOMICS, 62(2), 1999, pp. 216-222
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:
Kropp, S
Finkenstaedt, M
Laske, C
Schulz-Schaeffer, W
Zerr, I
Kretschmar, A
Poser, S
Citation: S. Kropp et al., Value of diffusion-weighted magnetic resonance image in Creutzfeldt-Jakob disease (vol 245, pg 395, 1998), J NEUROL, 246(1), 1999, pp. 66-66
Risultati:
1-11
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