| [O2–18–01]: TDP‐43 PATHOLOGY DISRUPTS NUCLEAR PORE COMPLEXES AND NUCLEOCYTOPLASMIC TRANSPORT IN ALS/FTD CC Chou, Y Zhang, M Umoh, NT Seyfried, M Powers, T Kukar, K Boylan, ... Alzheimer's & Dementia 13 (7S_Part_12), P602-P602, 2017 | | 2017 |
| [P1–254]: CHARACTERISTICS AND PROGRESS ON THE INITIAL 209 SUBJECTS IN THE LONGITUDINAL EVALUATION OF FAMILIAL FRONTOTEMPORAL DEMENTIA SUBJECTS (LEFFTDS) PROTOCOL CM Dheel, BF Boeve, HJ Rosen, AL Boxer, G Coppola, BC Dickerson, ... Alzheimer's & Dementia 13 (7S_Part_7), P345-P345, 2017 | | 2017 |
| [P2–140]: ABNORMAL CHROMOSOME COPY NUMBER AND ASSOCIATED NEURONAL CELL DEATH IN FRONTOTEMPORAL LOBAR DEGENERATION J Caneus, A Granic, R Rademakers, DW Dickson, CM Coughlan, ... Alzheimer's & Dementia 13 (7S_Part_13), P661-P661, 2017 | | 2017 |
| [P2–303]: ADVANCING RESEARCH AND TREATMENT IN FRONTOTEMPORAL LOBAR DEGENERATION (ARTFL) NORTH AMERICAN RARE DISEASE CLINICAL RESEARCH CONSORTIUM: PROGRESS AND CHARACTERIZATION … AL Boxer, HJ Rosen, BF Boeve, H Heuer, M Grossman, G Coppola, ... Alzheimer's & Dementia 13 (7S_Part_15), P733-P734, 2017 | | 2017 |
| [P2–317]: PHENOCONVERSION FROM ASYMPTOMATIC TO MINIMALLY SYMPTOMATIC FTLD: PRELIMINARY DATA IN THE LEFFTDS COHORT BF Boeve, H Rosen, A Boxer, G Coppola, C Dheel, BC Dickerson, ... Alzheimer's & Dementia 13 (7S_Part_15), P739-P739, 2017 | | 2017 |
| 1H MR Spectroscopy in Presymptomatic MAPT mutation carriers: A Biomarker for Tau Mediated Pathology K Kantarci, BF Boeve, ZK Wszolek, R Rademakers, JL Whitwell, ... Alzheimer's and Dementia 6 (4), 4, 2010 | | 2010 |
| 413 Reconsolidation: maintaining memory relevance G Perea, M Navarrete, A Araque, B Knöll, A Nordheim, VS Caviness Jr, ... | | |
| 647 On the origin of genomes and cells within inorganic compartments EV Koonin, W Martin, D Leister, B Dermaut, S Kumar-Singh, ... Genetics 21 (12), 633-692, 2005 | | 2005 |
| 756 Schymick, Yang, Andersen, et al W Robberecht, BOM Leuven, A Goate, RJ Caselli, M Hutton, J Gass, ... Brain 126, 2016-22, 2003 | | 2003 |
| A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD J Van Der Zee, R Rademakers, S Engelborghs, I Gijselinck, V Bogaerts, ... Brain 129 (4), 841-852, 2006 | 108 | 2006 |
| A belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD. Commentary J HARDY, P MOMENI, J CAEKEBEKE, T DE POOTER, K PEELERS, ... Brain 129, 2006 | | 2006 |
| A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories C Akimoto, AE Volk, M van Blitterswijk, M Van den Broeck, CS Leblond, ... Journal of medical genetics 51 (6), 419-424, 2014 | 149 | 2014 |
| A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers M Zhang, R Ferrari, MC Tartaglia, J Keith, EI Surace, U Wolf, C Sato, ... Brain 141 (10), 2895-2907, 2018 | 48 | 2018 |
| A Clinicopathological Report of Five Cases of FTLD-TDP Type E with Motor Neuron Disease X Zhou, S Koga, N Ghayal, M Baker, M DeTure, CF De Castro, S Roemer, ... JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY 79 (6), 697-697, 2020 | | 2020 |
| A familial form of parkinsonism, dementia, and motor neuron disease: A longitudinal study S Fujioka, BF Boeve, JE Parisi, P Tacik, N Aoki, AJ Strongosky, M Baker, ... Parkinsonism & related disorders 20 (11), 1129-1134, 2014 | 7 | 2014 |
| A Family With Corticobasal Degeneration, Parkinson’s Disease, Amyotrophic Lateral Sclerosis, and Dementia (P3. 085) S Fujioka, M Sanchez Contreras, A Strongosky, P Tacik, B Boeve, ... Neurology 82 (10_supplement), P3. 085, 2014 | | 2014 |
| A genome-wide search for novel early-onset Alzheimer disease genes M Cruts, R Rademakers, M Van den Broeck, CM van Duijn, ... Neurobiology of Aging, 128, 2000 | 1 | 2000 |
| A Kindred with Familial Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis Associated with the GGGGCC Repeat Expansion in C9ORF72 (P05.058) B Boeve, J Daube, M DeJesus-Hernandez, J Parisi, D Dickson, ... Neurology 78 (1_supplement), P05. 058-P05. 058, 2012 | | 2012 |
| A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech KA Josephs, JR Duffy, HM Clark, RL Utianski, EA Strand, MM Machulda, ... Nature communications 12 (1), 3452, 2021 | 52 | 2021 |
| A new subtype of frontotemporal lobar degeneration with FUS pathology M Neumann, R Rademakers, S Roeber, M Baker, HA Kretzschmar, ... Brain 132 (11), 2922-2931, 2009 | 888 | 2009 |
