White matter pathology and disconnection in the frontal lobe in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Craggs, Lucinda J. L., Yamamoto, Yumi, Ihara, Masafumi, Fenwick, Richard, Burke, Matthew, Oakley, Arthur E., Roeber, Sigrun, Duering, Marco, Kretzschmar, Hans, Kalaria, Raj N.
Published in Neuropathology and applied neurobiology (01.08.2014)
Published in Neuropathology and applied neurobiology (01.08.2014)
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Cerebral angiitis in four patients with chronic GVHD
Sostak, P, Padovan, C S, Eigenbrod, S, Roeber, S, Segerer, S, Schankin, C, Siegert, S, Saam, T, Theil, D, Kolb, H-J, Kretzschmar, H, Straube, A
Published in Bone marrow transplantation (Basingstoke) (01.07.2010)
Published in Bone marrow transplantation (Basingstoke) (01.07.2010)
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A Pair of Siblings with a rare R5H-Mutation in Exon 1 of the MAPT-Gene
Henz, S, Ackl, N, Knels, C, Rominger, A, Flatz, W, Teipel, S, Huppertz, H J, Roeber, S, Neumann, M, Danek, A
Published in Fortschritte der Neurologie-Psychiatrie (01.07.2015)
Published in Fortschritte der Neurologie-Psychiatrie (01.07.2015)
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A new subtype of frontotemporal lobar degeneration with FUS pathology
Neumann, Manuela, Rademakers, Rosa, Roeber, Sigrun, Baker, Matt, Kretzschmar, Hans A., Mackenzie, Ian R. A.
Published in Brain (London, England : 1878) (01.11.2009)
Published in Brain (London, England : 1878) (01.11.2009)
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Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD
Pottier, Cyril, Ren, Yingxue, Perkerson, Ralph B., Baker, Matt, Jenkins, Gregory D., van Blitterswijk, Marka, DeJesus-Hernandez, Mariely, van Rooij, Jeroen G. J., Murray, Melissa E., Christopher, Elizabeth, McDonnell, Shannon K., Fogarty, Zachary, Batzler, Anthony, Tian, Shulan, Vicente, Cristina T., Matchett, Billie, Karydas, Anna M., Hsiung, Ging-Yuek Robin, Seelaar, Harro, Mol, Merel O., Finger, Elizabeth C., Graff, Caroline, Öijerstedt, Linn, Neumann, Manuela, Heutink, Peter, Synofzik, Matthis, Wilke, Carlo, Prudlo, Johannes, Rizzu, Patrizia, Simon-Sanchez, Javier, Edbauer, Dieter, Diehl-Schmid, Janine, Evers, Bret M., King, Andrew, Mesulam, M. Marsel, Weintraub, Sandra, Geula, Changiz, Bieniek, Kevin F., Petrucelli, Leonard, Ahern, Geoffrey L., Reiman, Eric M., Woodruff, Bryan K., Caselli, Richard J., Huey, Edward D., Farlow, Martin R., Grafman, Jordan, Mead, Simon, Grinberg, Lea T., Spina, Salvatore, Irwin, David J., Lee, Edward B., Suh, EunRan, Snowden, Julie, Mann, David, Ertekin-Taner, Nilufer, Uitti, Ryan J., Wszolek, Zbigniew K., Josephs, Keith A., Parisi, Joseph E., Knopman, David S., Petersen, Ronald C., Hodges, John R., Piguet, Olivier, Geier, Ethan G., Yokoyama, Jennifer S., Rissman, Robert A., Rogaeva, Ekaterina, Keith, Julia, Zinman, Lorne, Tartaglia, Maria Carmela, Cairns, Nigel J., Cruchaga, Carlos, Kofler, Julia, Lopez, Oscar L., Beach, Thomas G., Arzberger, Thomas, Herms, Jochen, Honig, Lawrence S., Vonsattel, Jean Paul, Halliday, Glenda M., Kwok, John B., White, Charles L., Gearing, Marla, Glass, Jonathan, Rollinson, Sara, Pickering-Brown, Stuart, Rohrer, Jonathan D., Trojanowski, John Q., Van Deerlin, Vivianna, Bigio, Eileen H., Troakes, Claire, Asmann, Yan, Miller, Bruce L., Boeve, Bradley F., Seeley, William W., Mackenzie, Ian R. A., van Swieten, John C., Dickson, Dennis W., Biernacka, Joanna M., Rademakers, Rosa
Published in Acta neuropathologica (01.06.2019)
Published in Acta neuropathologica (01.06.2019)
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MRI characteristics and scoring in HDLS due to CSF1R gene mutations
Sundal, Christina, Van Gerpen, Jay A, Nicholson, Alexandra M, Wider, Christian, Shuster, Elizabeth A, Aasly, Jan, Spina, Salvatore, Ghetti, Bernardino, Roeber, Sigrun, Garbern, James, Borjesson-Hanson, Anne, Tselis, Alex, Swerdlow, Russell H, Miller, Bradley B, Fujioka, Shinsuke, Heckman, Michael G, Uitti, Ryan J, Josephs, Keith A, Baker, Matt, Andersen, Oluf, Rademakers, Rosa, Dickson, Dennis W, Broderick, Daniel, Wszolek, Zbigniew K
Published in Neurology (07.08.2012)
Published in Neurology (07.08.2012)
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"Hybrid tracheostomy": a low risk procedure for tracheostomy in COVID-19 patients
Nibbe, L, Jungehülsing, M, Röber, S, Ripberger, G, Oppert, M
Published in Medizinische Klinik, Intensivmedizin und Notfallmedizin (01.10.2020)
Published in Medizinische Klinik, Intensivmedizin und Notfallmedizin (01.10.2020)
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Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations
Sundal, Christina, Fujioka, Shinsuke, Van Gerpen, Jay A, Wider, Christian, Nicholson, Alexandra M, Baker, Matt, Shuster, Elizabeth A, Aasly, Jan, Spina, Salvatore, Ghetti, Bernardino, Roeber, Sigrun, Garbern, James, Tselis, Alex, Swerdlow, Russell H, Miller, Bradley B, Borjesson-Hanson, Anne, Uitti, Ryan J, Ross, Owen A, Stoessl, A. Jon, Rademakers, Rosa, Josephs, Keith A, Dickson, Dennis W, Broderick, Daniel, Wszolek, Zbigniew K
Published in Parkinsonism & related disorders (01.10.2013)
Published in Parkinsonism & related disorders (01.10.2013)
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Characterization of the human primary visual cortex and cerebellum proteomes using shotgun mass spectrometry-data-independent analyses
Martins-de-Souza, Daniel, Guest, Paul C., Guest, Francesca L., Bauder, Corinna, Rahmoune, Hassan, Pietsch, Sandra, Roeber, Sigrum, Kretzschmar, Hans, Mann, David, Baborie, Atik, Bahn, Sabine
Published in Proteomics (Weinheim) (01.02.2012)
Published in Proteomics (Weinheim) (01.02.2012)
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Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment
Roeber, Sigrun, Krebs, Bjarne, Neumann, Manuela, Windl, Otto, Zerr, Inga, Grasbon-Frodl, Eva-Maria, Kretzschmar, Hans A
Published in Acta neuropathologica (01.04.2005)
Published in Acta neuropathologica (01.04.2005)
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Identification of a second major locus for neurodegeneration with brain iron accumulation
Hartig, MB, Iuso, A, Kmiec, T, Jurkiewicz, E, Heim, K, Roeber, S, Krajewska-Walasek, M, Jozwiak, S, Hempel, M, Winkelmann, J, Haack, T, Elstner, M, Oexle, K, Klopstock, T, Mueller-Felber, W, Kretzschmar, H, Strom, TM, Meitinger, T, Prokisch, H
Published in Neuropediatrics (28.03.2011)
Published in Neuropediatrics (28.03.2011)
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Conference Proceeding
P117 Atypical clinical presentation in postmortem validated PSP
Respondek, G., Roeber, S., Apfelbacher, M., Gelpi, E., Gaig, C., Troakes, C., Chiu, W., van Swieten, J., Rajput, A., Kretzschmar, H., Oertel, W.H., Höglinger, G.
Published in Basal ganglia (01.03.2011)
Published in Basal ganglia (01.03.2011)
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Fatale familiäre Insomnie – Eine seltene Differentialdiagnose in der Demenzabklärung
Friedrich, M., Körte, R., Zerr, I., Roeber, S., Nacimiento, W.
Published in Aktuelle Neurologie (27.09.2006)
Published in Aktuelle Neurologie (27.09.2006)
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Conference Proceeding
Analysis and proposals for the management of a forest district with cupressus plantation in south Dafur (Sudan)
Roeber, S, Uibrig, H. (Technische Univ. Dresden, Tharandt (Germany). Fakultaet fuer Forst-, Geo- und Hydrowissenschaften. Inst. fuer Internationale Forst- und Holzwirtschaft)
Published in Beitraege fuer Forstwirtschaft und Landschaftsoekologie, Berlin (Germany) (1997)
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Published in Beitraege fuer Forstwirtschaft und Landschaftsoekologie, Berlin (Germany) (1997)
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