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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 Hits 1 – 20 of 22 1 Plasma tau is increased in frontotemporal dementia Foiani, Martha S; Woollacott, Ione OC; Heller, Carolin. - : BMJ Publishing Group Ltd, 2018 BASE Show details 2 Prevalence of Amyloid-β Pathology in Distinct Variants of Primary Progressive Aphasia Bergeron, David; Gorno-Tempini, Maria L.; Rabinovici, Gil D.. - 2018 BASE Show details 3 Prevalence of amyloid-β pathology in distinct variants of primary progressive aphasia: Amyloid-β Pathology in PPA Bergeron, David; Gorno-Tempini, Maria L.; Rabinovici, Gil D.... In: Annals of Neurology. - 84, 5 (2018) , 729-740, ISSN: 0364-5134 (2018) BASE Show details 4 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) Tang, Mengxuan; Ryman, Davis C.; McDade, Eric M.... In: Research outputs 2014 to 2021 (2016) BASE Show details 5 Patterns of longitudinal brain atrophy in the logopenic variant of primary progressive aphasia Rohrer, Jonathan D.; Caso, Francesca; Mahoney, Colin... In: Brain & language. - Orlando, Fla. [u.a.] : Elsevier 127 (2013) 2, 121-126 OLC Linguistik Show details 6 Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia Rohrer, Jonathan D; Beck, Jonathan; Plagnol, Vincent. - : BMJ Publishing Group Ltd, 2013 BASE Show details 7 Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia Rohrer, Jonathan D; Beck, Jonathan; Plagnol, Vincent. - : BMJ Publishing Group, 2013 BASE Show details 8 White matter tract signatures of the progressive aphasias Mahoney, Colin J.; Malone, Ian B.; Ridgway, Gerard R.. - : Elsevier, 2013 BASE Show details 9 Patterns of longitudinal brain atrophy in the logopenic variant of primary progressive aphasia Rohrer, Jonathan D.; Caso, Francesca; Mahoney, Colin. - : Academic Press, 2013 BASE Show details 10 Rates of hemispheric and lobar atrophy in the language variants of frontotemporal lobar degeneration Rohrer, Jonathan D.; Clarkson, Matthew J.; Kittus, Raivo. - 2012 BASE Show details 11 Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia Rascovsky, Katya; Hodges, John R.; Knopman, David. - : Oxford University Press, 2011 BASE Show details 12 Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia Rascovsky, Katya; Hodges, John R.; Knopman, David. - : Oxford University Press, 2011 BASE Show details 13 Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia Rascovsky, Katya; Hodges, John R.; Knopman, David. - : Oxford University Press, 2011 BASE Show details 14 Revising the definition of Alzheimer's disease: a new lexicon Dubois, Bruno; Feldman, Howard H; Jacova, Claudia. - 2010 BASE Show details 15 Revising the definition of Alzheimer's disease: a new lexicon ... Dubois, Bruno; Feldman, Howard H; Jacova, Claudia. - : Columbia University, 2010 BASE Show details 16 Word-finding difficulty: a clinical analysis of the progressive aphasias Rohrer, Jonathan D.; Knight, William D.; Warren, Jane E.... In: Brain. - Oxford : Oxford Univ. Press 131 (2008) 1, 8-38 BLLDB Show details 17 A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series Beck, Jonathan; Rohrer, Jonathan D.; Campbell, Tracy. - : Oxford University Press, 2008 BASE Show details 18 A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series Beck, Jonathan; Rohrer, Jonathan D.; Campbell, Tracy. - : Oxford University Press, 2008 BASE Show details 19 Word-finding difficulty: a clinical analysis of the progressive aphasias Rohrer, Jonathan D.; Knight, William D.; Warren, Jane E.. - : Oxford University Press, 2008 BASE Show details 20 A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series Beck, Jonathan; Rohrer, Jonathan D.; Campbell, Tracy. - 2008 BASE Show details Page: 1 2

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