Efficacy of flupirtine on cognitive function in patients with CJD: A double-blind study von Otto, M, Cepek, L, Ratzka, P, Doehlinger, S, Boekhoff, I, Wiltfang, J, Irle, E, Pergande, G, Ellers-Lenz, B, Windl, O, Kretzschmar, H A, Poser, S, Prange, H

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Concomitant TAR-DNA-Binding Protein 43 Pathology Is Present in Alzheimer Disease and Corticobasal Degeneration but Not in Other Tauopathies von Uryu, Kunihiro, Nakashima-Yasuda, Hanae, Forman, Mark S, Kwong, Linda K, Clark, Christopher M, Grossman, Murray, Miller, Bruce L, Kretzschmar, Hans A, Lee, Virginia M.-Y, Trojanowski, John Q, Neumann, Manuela

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Creutzfeldt-Jakob disease in Germany: a prospective 12-year surveillance von Heinemann, U., Krasnianski, A., Meissner, B., Varges, D., Kallenberg, K., Schulz-Schaeffer, W. J., Steinhoff, B. J., Grasbon-Frodl, E. M., Kretzschmar, H. A., Zerr, I.

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TDP-43 in the Ubiquitin Pathology of Frontotemporal Dementia With VCP Gene Mutations von Neumann, Manuela, Mackenzie, Ian R, Cairns, Nigel J, Boyer, Philip J, Markesbery, William R, Smith, Charles D, Taylor, J Paul, Kretzschmar, Hans A, Kimonis, Virginia E, Forman, Mark S

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Recruitment of neural precursor cells from circumventricular organs of patients with cerebral ischaemia von Sanin, V., Heeß, C., Kretzschmar, H. A., Schüller, U.

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14-3-3 CSF levels in sporadic Creutzfeldt–Jakob disease differ across molecular subtypes von Gmitterová, K, Heinemann, U, Bodemer, M, Krasnianski, A, Meissner, B, Kretzschmar, H.A, Zerr, I

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Diagnostic value of periodic complexes in Creutzfeldt-Jakob disease von Steinhoff, Bernhard J., Zerr, Inga, Glatting, Maya, Schulz-Schaeffer, Walter, Poser, Sigrid, Kretzschmar, Hans A.

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TDP-43-Positive White Matter Pathology in Frontotemporal Lobar Degeneration With Ubiquitin-Positive Inclusions von Neumann, Manuela, Kwong, Linda K, Truax, Adam C, Vanmassenhove, Ben, Kretzschmar, Hans A, Van Deerlin, Vivianna M, Clark, Chrisopher M, Grossman, Murray, Miller, Bruce L, Trojanowski, John Q, Lee, Virginia M.-Y

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Subcellular Localization of Wild-Type and Parkinson's Disease-Associated Mutant alpha -Synuclein in Human and Transgenic Mouse Brain von Kahle, Philipp J, Neumann, Manuela, Ozmen, Laurence, Muller, Veronika, Jacobsen, Helmut, Schindzielorz, Alice, Okochi, Masayasu, Leimer, Uwe, van der Putten, Herman, Probst, Alphonse, Kremmer, Elisabeth, Kretzschmar, Hans A, Haass, Christian

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Genetic prion disease : the EUROCJD experience von KOVACS, Gabor G, PUOPOLO, Maria, DELASNERIE-LAUPRETRE, Nicole, BRANDEL, Jean Philippe, ZERR, Inga, KRETZSCHMAR, Hans A, DE PEDRO-CUESTA, Jesus, CALERO-LARA, Miguel, GLATZEL, Markus, AGUZZI, Adriano, BISHOP, Matthew, KNIGHT, Richard, LADOGANA, Anna, BELAY, Girma, WILL, Robert, MITROVA, Eva, POCCHIARI, Maurizio, BUDKA, Herbert, VAN DUIJN, Cornelia, COLLINS, Steven J, BOYD, Alison, GIULIVI, Antonio, COULTHART, Mike

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Tau protein and 14-3-3 protein in the differential diagnosis of Creutzfeldt-Jakob disease von OTTO, M, WILTFANG, J, CEPEK, L, NEUMANN, M, MOLLENHAUER, B, STEINACKER, P, CIESIELCZYK, B, SCHULZ-SCHAEFFER, W, KRETZSCHMAR, H. A, POSER, S

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Pattern of Cortical Changes in Sporadic Creutzfeldt-Jakob Disease von Tschampa, H.J, Kallenberg, K, Kretzschmar, H.A, Meissner, B, Knauth, M, Urbach, H, Zerr, I

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Predictors of survival in sporadic Creutzfeldt–Jakob disease and other human transmissible spongiform encephalopathies von Pocchiari, M., Puopolo, M., Croes, E. A., Budka, H., Gelpi, E., Collins, S., Lewis, V., Sutcliffe, T., Guilivi, A., Delasnerie-Laupretre, N., Brandel, J.-P., Alperovitch, A., Zerr, I., Poser, S., Kretzschmar, H. A., Ladogana, A., Rietvald, I., Mitrova, E., Martinez-Martin, P., de Pedro-Cuesta, J., Glatzel, M., Aguzzi, A., Cooper, S., Mackenzie, J., van Duijn, C. M., Will, R. G.

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Early Spread of Scrapie from the Gastrointestinal Tract to the Central Nervous System Involves Autonomic Fibers of the Splanchnic and Vagus Nerves von McBride, P A, Schulz-Schaeffer, W J, Donaldson, M, Bruce, M, Diringer, H, Kretzschmar, H A, Beekes, M

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Role of microglia and host prion protein in neurotoxicity of a prion protein fragment von Brown, David R, Schmidt, Bernhard, Kretzschmar, Hans A

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Role of copper and manganese in prion disease progression von Mitteregger, Gerda, Korte, Stefan, Shakarami, Mehdi, Herms, Jochen, Kretzschmar, Hans A

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Identification of Differentially Expressed Genes in Scrapie-Infected Mouse Brains by Using Global Gene Expression Technology von Xiang, Wei, Windl, Otto, Wünsch, Gerda, Dugas, Martin, Kohlmann, Alexander, Dierkes, Nicola, Westner, Ingo M, Kretzschmar, Hans A

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Misfolded proteinase K–resistant hyperphosphorylated α-synuclein in aged transgenic mice with locomotor deterioration and in human α-synucleinopathies von Neumann, Manuela, Kahle, Philipp J., Giasson, Benoit I., Ozmen, Laurence, Borroni, Edilio, Spooren, Will, Müller, Veronika, Odoy, Sabine, Fujiwara, Hideo, Hasegawa, Masato, Iwatsubo, Takeshi, Trojanowski, John Q., Kretzschmar, Hans A., Haass, Christian

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Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob disease von Zerr, Inga, Bodemer, Monika, Gefeller, Olaf, Otto, Markus, Poser, Sigrid, Wiltfang, Jens, Windl, Otto, Kretzschmar, Hans A., Weber, Thomas

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Hyperphosphorylation and insolubility of α-synuclein in transgenic mouse oligodendrocytes von Kahle, Philipp J, Neumann, Manuela, Ozmen, Laurence, Müller, Veronika, Jacobsen, Helmut, Spooren, Will, Fuss, Babette, Mallon, Barbara, Macklin, Wendy B, Fujiwara, Hideo, Hasegawa, Masato, Iwatsubo, Takeshi, Kretzschmar, Hans A, Haass, Christian

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