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The Lancet Neurology, ISSN 1474-4422, 2015, Volume 14, Issue 3, pp. 253 - 262
Journal Article
Nature Communications, ISSN 2041-1723, 10/2018, Volume 9, Issue 1, pp. 4273 - 16
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 02/2015, Volume 23, Issue 2, pp. 224 - 228
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 867 - 876
Journal Article
Genetics in medicine : official journal of the American College of Medical Genetics, ISSN 1098-3600, 03/2019, Volume 21, Issue 3, pp. 764 - 765
A correction has been published to this Article. The PDF and HTML have been updated accordingly. 
Journal Article
Journal Article
NeuroImage: Clinical, ISSN 2213-1582, 2017, Volume 15, pp. 171 - 180
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 02/2018, Volume 62, pp. 191 - 196
Frontotemporal dementia (FTD) is a highly heritable condition with multiple genetic causes. In this study, similarities and differences of gray matter (GM)... 
Atrophy | Magnetic resonance imaging | Frontotemporal dementia | Voxel-based morphometry | Preclinical dementia | LOBAR DEGENERATION | ALZHEIMERS-DISEASE | MUTATION CARRIERS | TAU | PROGRANULIN | C9ORF72 | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | NETWORK CONNECTIVITY | BEHAVIORAL VARIANT | Gene mutations | Genetic research
Journal Article