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Number of items: 42.

Traber, G L; Pangalu, A; Neumann, M; Costa, J; Weller, M; Huna-Baron, R; Landau, K (2015). Malignant optic glioma - the spectrum of disease in a case series. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie, 253(7):1187-1194.

Jung, H H; Neumann, M; Bloch, K E (2012). Amyotrophic lateral sclerosis - diagnosis and treatment. Praxis, 101(14):907-914.

Martory, M D; Roth, S; Lövblad, K O; Neumann, M; Lobrinus, J A; Assal, F (2012). Creutzfeldt-Jakob disease revealed by a logopenic variant of primary progressive aphasia. European Neurology, 67(6):360-362.

Neumann, M (2012). Nicht-Alzheimer-Demenzen. In: Paulus, W; Schröder, J M. Pathologie. Neuropathologie (3., neubearb. Aufl.). Berlin, DE: Springer, 209-222.

Mackenzie, I R A; Neumann, M; Baborie, A; Sampathu, D M; Du Plessis, D; Jaros, E; Perry, R H; Trojanowski, J Q; Mann, D M A; Lee, V M Y (2011). A harmonized classification system for FTLD-TDP pathology. Acta Neuropathologica, 122(1):111-113.

Kellner, O; Sabova, K; Neumann, M; Jung, H H (2011). Die schwierige Diagnose der kortikobasalen Degeneration: Unterscheidung zwischen klinischem Syndrom und pathologischer Diagnose. Fortschritte der Neurologie, Psychiatrie, 79(11):660-667.

Mackenzie, I R A; Munoz, D G; Kusaka, H; Yokota, O; Ishihara, K; Roeber, S; Kretzschmar, H A; Cairns, N J; Neumann, M (2011). Distinct pathological subtypes of FTLD-FUS. Acta Neuropathologica, 121(2):207-218.

Neumann, M; Bentmann, E; Dormann, D; Jawaid, A; DeJesus-Hernandez, M; Ansorge, O; Roeber, S; Kretzschmar, H A; Munoz, D G; Kusaka, H; Yokota, O; Ang, L C; Bilbao, J; Rademakers, R; Haass, C; Mackenzie, I R A (2011). FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations. Brain: A Journal of Neurology, 134(9):2595-2609.

Neumann, M; Mackenzie, I R A (2011). Frontotemporal lobar degeneration with FUS immunoreactive inclusions. In: Dickson, D W; Weller, R O. Neurodegeneration: The molecular pathology of dementia and movement disorders (2nd ed.). Chicester, UK: Wiley-Blackwell, 412-417.

Mackenzie, I R A; Neumann, M (2011). Frontotemporal lobar degeneration with TDP-43 pathology. In: Dickson, D W; Weller, R O. Neurodegeneration: The molecular pathology of dementia and movement disorders (2nd ed.). Chicester, UK: Wiley-Blackwell, 393-403.

Otto, M; Ludolph, A C; Landwehrmeyer, B; Förstl, H; Diehl-Schmid, J; Neumann, M; Kretzschmar, H A; Schroeter, M; Kornhuber, J; Danek, A (2011). Konsortium zur Erforschung der frontotemporalen Lobärdegeneration. Der Nervenarzt, 82(8):1002-1005.

Josephs, K A; Hodges, J R; Snowden, J S; Mackenzie, I R A; Neumann, M; Mann, D M; Dickson, D W (2011). Neuropathological background of phenotypical variability in frontotemporal dementia. Acta Neuropathologica, 122(2):137-153.

Mackenzie, I R A; Neumann, M; Cairns, N J; Munoz, D G; Isaacs, A M (2011). Novel types of frontotemporal lobar degeneration: beyond tau and TDP-43. Journal of Molecular Neuroscience, 45(3):402-408.

Rieker, C; Engblom, D; Kreiner, G; Domanskyi, A; Schoberer, A; Stotz, S; Neumann, M; Yuan, X; Grummt, I; Schütz, G; Parlato, R (2011). Nucleolar disruption in dopaminergic neurons leads to oxidative damage and parkinsonism through repression of mammalian target of rapamycin signaling. Journal of Neuroscience, 31(2):453-460.

Mackenzie, I R A; Ansorge, O; Strong, M; Bilbao, J; Zinman, L; Ang, L C; Baker, M; Stewart, H; Eisen, A; Rademakers, R; Neumann, M (2011). Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation. Acta Neuropathologica, 122(1):87-98.

Garbern, J Y; Neumann, M; Trojanowski, J Q; Lee, V M Y; Feldman, G; Norris, J W; Friez, M J; Schwartz, C E; Stevenson, R; Sima, A A F (2010). A mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition. Brain: A Journal of Neurology, 133(Pt 5):1391-1402.

Dormann, D; Rodde, R; Edbauer, D; Bentmann, E; Fischer, I; Hruscha, A; Than, M E; Mackenzie, I R A; Capell, A; Schmid, B; Neumann, M; Haass, C (2010). ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import. The EMBO Journal, 29(16):2841-2857.

Van Deerlin, V M; Sleiman, P M A; Martinez-Lage, M; Chen-Plotkin, A; Wang, L S; Graff-Radford, N R; Dickson, D W; Rademakers, R; Boeve, B F; Grossman, M; Arnold, S E; Mann, D M A; Pickering-Brown, S M; Seelaar, H; Heutink, P; van Swieten, J C; Murrell, J R; Ghetti, B; Spina, S; Grafman, J; Hodges, J; Spillantini, M G; Gilman, S; Lieberman, A P; Kaye, J A; Woltjer, R L; Bigio, E H; Mesulam, M; Al-Sarraj, S; Troakes, C; Rosenberg, R N; White, C L; Ferrer, I; Lladó, A; Neumann, M; Kretzschmar, H A; Hulette, C M; Welsh-Bohmer, K A; Miller, B L; Alzualde, A; Lopez de Munain, A; McKee, A C; Gearing, M; Levey, A I; Lah, J J; Hardy, J; Rohrer, J D; Lashley, T; Mackenzie, I R A; Feldman, H H; Hamilton, R L; Dekosky, S T; van der Zee, J; Kumar-Singh, S; Van Broeckhoven, C; Mayeux, R; Vonsattel, J P G; Troncoso, J C; Kril, J J; Kwok, J B J; Halliday, G M; Bird, T D; Ince, P G; Shaw, P J; Cairns, N J; Morris, J C; McLean, C A; DeCarli, C; Ellis, W G; Freeman, S H; Frosch, M P; Growdon, J H; Perl, D P; Sano, M; Bennett, D A; Schneider, J A; Beach, T G; Reiman, E M; Woodruff, B K; Cummings, J; Vinters, H V; Miller, C A; Chui, H C; Alafuzoff, I; Hartikainen, P; Seilhean, D; Galasko, D; Masliah, E; Cotman, C W; Tuñón, M T; Martínez, M C C; Munoz, D G; Carroll, S L; Marson, D; Riederer, P F; Bogdanovic, N; Schellenberg, G D; Hakonarson, H; Trojanowski, J Q; Lee, V M Y (2010). Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Nature Genetics, 42(3):234-239.

Fiesel, F C; Voigt, A; Weber, S S; Van den Haute, C; Waldenmaier, A; Görner, K; Walter, M; Anderson, M L; Kern, J V; Rasse, T M; Schmidt, T; Springer, W; Kirchner, R; Bonin, M; Neumann, M; Baekelandt, V; Alunni-Fabbroni, M; Schulz, J B; Kahle, P J (2010). Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6. The EMBO Journal, 29(1):209-221.

Mackenzie, I R A; Neumann, M; Bigio, E H; Cairns, N J; Alafuzoff, I; Kril, J; Kovacs, G G; Ghetti, B; Halliday, G; Holm, I E; Ince, P G; Kamphorst, W; Revesz, T; Rozemuller, A J M; Kumar-Singh, S; Akiyama, H; Baborie, A; Spina, S; Dickson, D W; Trojanowski, J Q; Mann, D M A (2010). Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update. Acta Neuropathologica, 119(1):1-4.

Waibel, S; Neumann, M; Rabe, M; Meyer, T; Ludolph, A C (2010). Novel missense and truncating mutations in FUS/TLS in familial ALS. Neurology, 75(9):815-817.

Mackenzie, I R A; Rademakers, R; Neumann, M (2010). TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia. Lancet Neurology, 9(10):995-1007.

Ritson, G P; Custer, S K; Freibaum, B D; Guinto, J B; Geffel, D; Moore, J; Tang, W; Winton, M J; Neumann, M; Trojanowski, J Q; Lee, V M Y; Forman, M S; Taylor, J P (2010). TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97. Journal of Neuroscience, 30(22):7729-7739.

Yu, C E; Bird, T D; Bekris, L M; Montine, T J; Leverenz, J B; Steinbart, E; Galloway, N M; Feldman, H; Woltjer, R; Miller, C A; Wood, E; Grossman, M; McCluskey, L; Clark, C M; Neumann, M; Danek, A; Galasko, D R; Arnold, S E; Chen-Plotkin, A; Karydas, A; Miller, B L; Trojanowski, J Q; Lee, V M Y; Schellenberg, G D; Van Deerlin, V M (2010). The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Archives of Neurology, 67(2):161-170.

Custer, S K; Neumann, M; Lu, H; Wright, A C; Taylor, J P (2010). Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone. Human Molecular Genetics, 19(9):1741-1755.

Neumann, M; Tolnay, M; Mackenzie, I R A (2009). The molecular basis of frontotemporal dementia. Expert Reviews in Molecular Medicine, 11:e23.

Geser, F; Martinez-Lage, M; Robinson, J; Uryu, K; Neumann, M; Brandmeir, N J; Xie, S X; Kwong, L K; Elman, L; McCluskey, L; Clark, C M; Malunda, J; Miller, B L; Zimmerman, E A; Qian, J; Van Deerlin, V; Grossman, M; Lee, V M Y; Trojanowski, J Q (2009). Clinical and pathological continuum of multisystem TDP-43 proteinopathies. Archives of Neurology, 66(2):180-189.

Neumann, M (2009). Phenotypic heterogeneity and genetic modifiers in prion disease caused by a Pro102Leu mutation in the PRNP gene. Nature Clinical Practice Neurology, 5(2):68-69.

Neumann, M; Rademakers, R; Roeber, S; Baker, M; Kretzschmar, H A; Mackenzie, I R A (2009). A new subtype of frontotemporal lobar degeneration with FUS pathology. Brain: A Journal of Neurology, 132(Pt 11):2922-2931.

Neumann, M; Roeber, S; Kretzschmar, H A; Rademakers, R; Baker, M; Mackenzie, I R A (2009). Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease. Acta Neuropathologica, 118(5):605-616.

Wüllner, U; Schmitt, I; Kammal, M; Kretzschmar, H A; Neumann, M (2009). Definite multiple system atrophy in a German family. Journal of Neurology, Neurosurgery, and Psychiatry, 80(4):449-450.

Igaz, L M; Kwong, L K; Chen-Plotkin, A; Winton, M J; Unger, T L; Xu, Y; Neumann, M; Trojanowski, J Q; Lee, V M Y (2009). Expression of TDP-43 C-terminal fragments in vitro recapitulates pathological features of TDP-43 proteinopathies. Journal of Biological Chemistry, 284(13):8516-8524.

Munoz, D G; Neumann, M; Kusaka, H; Yokota, O; Ishihara, K; Terada, S; Kuroda, S; Mackenzie, I R A (2009). FUS pathology in basophilic inclusion body disease. Acta Neuropathologica, 118(5):617-627.

Danek, A; Diehl-Schmid, J; Grimmer, T; Laws, S M; Neumann, M; Perneczky, R; Riemenschneider, M; Kurz, A; Förstl, H (2009). Frontotemporale Lobärdegenerationen. Teil 1: Diagnose und Therapie. Fortschritte der Neurologie, Psychiatrie, 77(3):169-176; quiz 177-179.

Diehl-Schmid, J; Neumann, M; Laws, S M; Perneczky, R; Grimmer, T; Danek, A; Kurz, A; Riemenschneider, M; Förstl, H (2009). Frontotemporale Lobärdegenerationen. Teil 2: Bildgebung, Neuropathologie und Genetik. Fortschritte der Neurologie, Psychiatrie, 77(5):295-304.

Neumann, M (2009). Molecular neuropathology of TDP-43 proteinopathies. International Journal of Molecular Sciences, 10(1):232-246.

Mackenzie, I R A; Neumann, M; Bigio, E H; Cairns, N J; Alafuzoff, I; Kril, J; Kovacs, G G; Ghetti, B; Halliday, G; Holm, I E; Ince, P G; Kamphorst, W; Revesz, T; Rozemuller, A J M; Kumar-Singh, S; Akiyama, H; Baborie, A; Spina, S; Dickson, D W; Trojanowski, J Q; Mann, D M A (2009). Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations. Acta Neuropathologica, 117(1):15-18.

Schell, H; Hasegawa, T; Neumann, M; Kahle, P J (2009). Nuclear and neuritic distribution of serine-129 phosphorylated alpha-synuclein in transgenic mice. Neuroscience, 160(4):796-804.

Neumann, M; Kwong, L K; Lee, E B; Kremmer, E; Flatley, A; Xu, Y; Forman, M S; Troost, D; Kretzschmar, H A; Trojanowski, J Q; Lee, V M Y (2009). Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies. Acta Neuropathologica, 117(2):137-149.

Dormann, D; Capell, A; Carlson, A M; Shankaran, S S; Rodde, R; Neumann, M; Kremmer, E; Matsuwaki, T; Yamanouchi, K; Nishihara, M; Haass, C (2009). Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin. Journal of Neurochemistry, 110(3):1082-1094.

Lippa, C F; Rosso, A L; Stutzbach, L D; Neumann, M; Lee, V M Y; Trojanowski, J Q (2009). Transactive response DNA-binding protein 43 burden in familial Alzheimer disease and Down syndrome. Archives of Neurology, 66(12):1483-1488.

Güntert, G (2006). Alfieri e Bocage. Auto-retratos en forma de soneto. In: Neumann, M. Zwischen allen Stühlen : Manuel Maria de Barbosa du Bocage : Akten des Kolloquiums zum 200. Todesjahr des Dichters, Hamburg, 20.-22. Juni 2005. Bonn: Romanistischer Verlag, 55-77.

This list was generated on Tue Jul 25 21:50:56 2017 CEST.