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Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes
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Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS)
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Local feature suppression effect in face and non-face stimuli
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Facilitation of word retrieval in primary progressive aphasia
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The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration
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In: 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. (2010)
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Frontotemporale Lobardegenerationen, Teil 2: Bildgebung, Neuropathologie und Genetik
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In: Research outputs pre 2011 (2009)
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Frontotemporale Lobardegenerationen, Teil 1: Diagnose und Therapie
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In: Research outputs pre 2011 (2009)
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