Rates of lobar atrophy in asymptomatic MAPT mutation carriers

[1]  Rogier A. Feis,et al.  Gray and white matter changes in presymptomatic genetic frontotemporal dementia: a longitudinal MRI study , 2019, Neurobiology of Aging.

[2]  S. Rombouts,et al.  Longitudinal multimodal MRI as prognostic and diagnostic biomarker in presymptomatic familial frontotemporal dementia , 2018, Brain : a journal of neurology.

[3]  Nick C Fox,et al.  Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales , 2018, Alzheimer's research & therapy.

[4]  S. Ourselin,et al.  Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study , 2018, Neurobiology of Aging.

[5]  Shannon L. Risacher,et al.  Alzheimer disease brain atrophy subtypes are associated with cognition and rate of decline , 2017, Neurology.

[6]  J. Kramer,et al.  Longitudinal white matter change in frontotemporal dementia subtypes and sporadic late onset Alzheimer's disease , 2017, NeuroImage: Clinical.

[7]  Knut Engedal,et al.  Frontotemporal Dementia , 2016, Journal of geriatric psychiatry and neurology.

[8]  D. Louis Collins,et al.  Assessing atrophy measurement techniques in dementia: Results from the MIRIAD atrophy challenge , 2015, NeuroImage.

[9]  S. Fahn,et al.  Closing the tau loop: the missing tau mutation. , 2015, Brain : a journal of neurology.

[10]  C. Jack,et al.  Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images , 2015, European journal of neurology.

[11]  Veronica Redaelli,et al.  Presymptomatic cognitive and neuroanatomical changes in genetic frontotemporal dementia in the Genetic Frontotemporal dementia Initiative (GENFI) study: a cross-sectional analysis , 2015, The Lancet Neurology.

[12]  Nick C Fox,et al.  Longitudinal Diffusion Tensor Imaging in Frontotemporal Dementia , 2014, Annals of neurology.

[13]  C. Jack,et al.  MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodies , 2013, Neurology.

[14]  Andrew J. Saykin,et al.  The pattern of atrophy in familial Alzheimer disease , 2013, Neurology.

[15]  Ilya M. Veer,et al.  Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia , 2013, Neurology.

[16]  J. Rohrer,et al.  Phenotypic signatures of genetic frontotemporal dementia. , 2011, Current opinion in neurology.

[17]  David T. Jones,et al.  Altered functional connectivity in asymptomatic MAPT subjects , 2011, Neurology.

[18]  Clifford R. Jack,et al.  Time-to-event voxel-based techniques to assess regional atrophy associated with MCI risk of progression to AD , 2011, NeuroImage.

[19]  Sébastien Ourselin,et al.  Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations☆ , 2010, NeuroImage.

[20]  C. Jack,et al.  MRS in presymptomatic MAPT mutation carriers , 2010, Neurology.

[21]  C R Jack,et al.  Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations , 2009, Neurology.

[22]  C R Jack,et al.  Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN , 2009, Neurology.

[23]  Clifford R. Jack,et al.  Antemortem MRI based STructural Abnormality iNDex (STAND)-scores correlate with postmortem Braak neurofibrillary tangle stage , 2008, NeuroImage.

[24]  Brian B. Avants,et al.  Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain , 2008, Medical Image Anal..

[25]  D. Kareken,et al.  The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family , 2007, Brain : a journal of neurology.

[26]  C. Jack,et al.  Patterns of atrophy differ among specific subtypes of mild cognitive impairment. , 2007, Archives of neurology.

[27]  B. Boeve,et al.  Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation). , 2007, Parkinsonism & related disorders.

[28]  R. Uitti,et al.  Frontotemporal dementia and parkinsonism linked to chromosome 17 with the N279K tau mutation , 2007, Neuropathology : official journal of the Japanese Society of Neuropathology.

[29]  S. Feinstein,et al.  FTDP-17 Mutations Compromise the Ability of Tau to Regulate Microtubule Dynamics in Cells* , 2006, Journal of Biological Chemistry.

[30]  Karl J. Friston,et al.  Unified segmentation , 2005, NeuroImage.

[31]  T. Ferman,et al.  Early and pre-symptomatic neuropsychological dysfunction in the PPND family with the N279K tau mutation. , 2003, Parkinsonism & Related Disorders.

[32]  M. Spillantini,et al.  Tau gene mutations: dissecting the pathogenesis of FTDP-17. , 2002, Trends in molecular medicine.

[33]  Z. Wszolek,et al.  Physiologic assessment of autonomic dysfunction in pallidopontonigral degeneration with N279K mutation in the tau gene on chromosome 17 , 2002, Autonomic Neuroscience.

[34]  N. Tzourio-Mazoyer,et al.  Automated Anatomical Labeling of Activations in SPM Using a Macroscopic Anatomical Parcellation of the MNI MRI Single-Subject Brain , 2002, NeuroImage.

[35]  R. Kardon,et al.  Frontotemporal dementia and parkinsonism linked to chromosome 17. , 2011, Folia neuropathologica.

[36]  R. Uitti,et al.  Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene , 2000, Neurology.

[37]  S. Deprima,et al.  Pseudoulnar palsy from a small infarct of the precentral knob , 2000, Neurology.

[38]  K. Arima,et al.  Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene , 2000, Neurology.

[39]  Ronald C. Petersen,et al.  Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.

[40]  B. Snow,et al.  Rapidly progressive autosomal dominant parkinsonism and dementia with pallido‐ponto‐nigral degeneration , 1992, Annals of neurology.