{"id":"W2138190873","doi":"10.1212/wnl.0b013e31821103e6","title":"Classification of primary progressive aphasia and its variants","year":2011,"lang":"en","type":"article","venue":"Neurology","topic":"Genomics and Rare Diseases","field":"Biochemistry, Genetics and Molecular Biology","cited_by":5112,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"National Center for Research Resources; National Institute on Deafness and Other Communication Disorders; National Institute on Aging; Australian Research Council; National Institutes of Health; University of Oxford; Vlaamse regering; KU Leuven; Bristol-Myers Squibb; Forest Laboratories; Canadian Institutes of Health Research; Fonds Wetenschappelijk Onderzoek; Elan; Eisai; National Institute of Neurological Disorders and Stroke; University of Cambridge; Natural Sciences and Engineering Research Council of Canada; Baxter International; Pfizer; Heart and Stroke Foundation of Canada; Canadian Stroke Network; Wellcome Trust; GlaxoSmithKline; Alzheimer Society; H. Lundbeck A/S; Myriad Genetics; Eli Lilly and Company; Sanofi; Alzheimer's Association; U.S. Department of Veterans Affairs","keywords":"Primary progressive aphasia; Consistency (knowledge bases); Operationalization; Natural language processing; Computer science; Reliability (semiconductor); Aphasia; Medicine; Psychology; Artificial intelligence; Pathology; Frontotemporal dementia; Cognitive psychology; Disease; Dementia","routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":true},"retraction":null,"screen":null}