Browsing by Author Neumann, Manuela

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Issue DateTitleAuthor(s)Citation
2010FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degenerationKril, Jillian; Authier, Astrid; Brown, Jeremy; Dickson, Dennis W.; et, al; Graff-Radford, Neill R.; Holm, Ida; Johannsen, Peter; Josephs, Keith; Mackenzie, Ian R. A.; Neumann, Manuela; Nielsen, Jorgen; Rademakers, Rosa; Rohrer, Jonathan; Seelaar, Harro; Urwin, Hazel; Van Swieten, John; Central Clinical School: MedicineFUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration, Acta Neuropathologica, vol.120, 1,pp 33-41
2013Mutations in protein N-arginine methyltransferases are not the cause of FTLD-FUSKril, Jillian; Baker, Matt; Boeve, Bradley; Dickson, Dennis; Halliday, Glenda; Josephs, Keith; Mackenzie, Ian; Neumann, Manuela; Petersen, Ronald; Rademakers, Rosa; Ravenscroft, Thomas; Rutherford, Nicola; Seeley, William; van Swieten, John; Central Clinical School: MedicineMutations in protein N-arginine methyltransferases are not the cause of FTLD-FUS, Neurobiology of Aging, vol.34, 9, 2013,pp 2235.e11-2235.e13
2015Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortiumGraeber, Manuel; Alafuzoff, I; Al-Saraj, S; Arzberger, Thomas; Bodi, Istvan; Bogdanovic, Nenad; Bugiani, Orso; et al, Various; Ferrer, I; Gelpi, Ellen; Neumann, Manuela; Pikkarainen, Maria; School of Medical Sciences: Brain and Mind CentreNeuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium, Journal of Neural Transmission, vol.122, 7, 2015,pp 957-972
2014TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansionsKril, Jillian; Al‑Sarraj, Safa; Elman, Lauren; et al, Various; Gallagher, Michael D; Gelpi, Ellen; Ghetti, Bernardino; Grossman, Murray; McCluskey, Leo; Neumann, Manuela; Suh, Eunran; van Swieten, John; Central Clinical School: MedicineTMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions, Acta Neuropathologica, vol.127, 3, 2014,pp 407-418