| P50 | author | David S Knopman | Q63967707 |
| | Zbigniew K Wszolek | Q64754704 |
| | Bradley F Boeve | Q67501037 |
| | Jonathan Graff-Radford | Q83230600 |
| | Kejal Kantarci | Q83230766 |
| | Adam L Boxer | Q87489100 |
| | Howard J Rosen | Q87844143 |
| | Maria I Lapid | Q90817729 |
| | Neill R Graff-Radford | Q91360658 |
| | Julie Fields | Q96196870 |
| | Timothy G Lesnick | Q114336660 |
| | Ralitza H Gavrilova | Q114336668 |
| | Christina M Dheel | Q114336731 |
| | Debra J Gearhart | Q114336732 |
| | Jeremy A Syrjanen | Q114336736 |
| | Leah K Forsberg | Q114336766 |
| | Danielle E Brushaber | Q114336772 |
| | LEFFTDS Consortium | Q114336885 |
| | Rosa Rademakers | Q28777946 |
| | Matthew L Senjem | Q30505707 |
| | Clifford Jack | Q30505709 |
| P2093 | author name string | David T Jones | |
| | Qin Chen | |
| | Walter K Kremers | |
| | Nirubol Tosakulwong | |
| P2860 | cites work | Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia | Q46080645 |
| | Alzheimer disease brain atrophy subtypes are associated with cognition and rate of decline | Q47588927 |
| | Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study | Q47952076 |
| | Frontotemporal dementia and Parkinsonism linked to chromosome 17 with the N279K tau mutation | Q48263968 |
| | Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation). | Q48323127 |
| | Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17. | Q48422650 |
| | Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene | Q49124703 |
| | Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation. | Q50720109 |
| | Frontotemporal dementia. | Q53268278 |
| | Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales. | Q55317633 |
| | Longitudinal multimodal MRI as prognostic and diagnostic biomarker in presymptomatic familial frontotemporal dementia | Q60923357 |
| | Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene | Q73766415 |
| | Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration | Q74300563 |
| | Gray and white matter changes in presymptomatic genetic frontotemporal dementia: a longitudinal MRI study | Q91317752 |
| | Automated Anatomical Labeling of Activations in SPM Using a Macroscopic Anatomical Parcellation of the MNI MRI Single-Subject Brain | Q25855787 |
| | Closing the tau loop: the missing tau mutation | Q27303641 |
| | Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17 | Q28274687 |
| | Unified segmentation | Q29616050 |
| | Antemortem MRI based STructural Abnormality iNDex (STAND)-scores correlate with postmortem Braak neurofibrillary tangle stage | Q33345777 |
| | MRS in presymptomatic MAPT mutation carriers: a potential biomarker for tau-mediated pathology | Q34125535 |
| | Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations | Q34134801 |
| | Tau gene mutations: dissecting the pathogenesis of FTDP-17. | Q34163214 |
| | Time-to-event voxel-based techniques to assess regional atrophy associated with MCI risk of progression to AD. | Q34380374 |
| | Symmetric diffeomorphic image registration with cross-correlation: evaluating automated labeling of elderly and neurodegenerative brain | Q34656983 |
| | Longitudinal diffusion tensor imaging in frontotemporal dementia. | Q35008632 |
| | Altered functional connectivity in asymptomatic MAPT subjects: a comparison to bvFTD | Q35183555 |
| | Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images | Q35327928 |
| | Assessing atrophy measurement techniques in dementia: Results from the MIRIAD atrophy challenge | Q36251868 |
| | Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia. | Q36687146 |
| | Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN | Q37180625 |
| | The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family | Q37243415 |
| | The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study | Q37251058 |
| | MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodies | Q37265436 |
| | Patterns of atrophy differ among specific subtypes of mild cognitive impairment | Q37326509 |
| | Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations | Q37368352 |
| | Phenotypic signatures of genetic frontotemporal dementia | Q37944092 |
| | Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis. | Q39041947 |
| | Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration | Q39100355 |
| | Longitudinal white matter change in frontotemporal dementia subtypes and sporadic late onset Alzheimer's disease | Q42364423 |
| | FTDP-17 mutations compromise the ability of tau to regulate microtubule dynamics in cells | Q43519306 |
| P304 | page(s) | 338-346 | |
| P577 | publication date | 2019-07-30 | |
| P1433 | published in | Alzheimer's & dementia (New York, N. Y.) | Q27726239 |
| P1476 | title | Rates of lobar atrophy in asymptomatic MAPT mutation carriers | |
| P478 | volume | 5 | |