Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images
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C. Jack | J. Gunter | R. Petersen | B. Boeve | M. Senjem | S. Weigand | D. Knopman | J. Whitwell | Z. Wszolek | M. Baker | K. Josephs | C. Jack | S. D. Weigand | J. L. Whitwell | B. F. Boeve | R. C. Petersen | M. L. Senjem | J. L. Gunter | M. C. Baker | M. DeJesus‐Hernandez | D. S. Knopman | Z. K. Wszolek | R. Rademakers | C. R. Jack | K. A. Josephs | J. Whitwell | R. Rademakers | M. Dejesus‐Hernandez
[1] Emma B. Lewis,et al. Correction of differential intensity inhomogeneity in longitudinal MR images , 2004, NeuroImage.
[2] Sébastien Ourselin,et al. Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations☆ , 2010, NeuroImage.
[3] Nick C. Fox,et al. The boundary shift integral: an accurate and robust measure of cerebral volume changes from registered repeat MRI , 1997, IEEE Transactions on Medical Imaging.
[4] C. Jack,et al. 11C PiB and structural MRI provide complementary information in imaging of Alzheimer's disease and amnestic mild cognitive impairment. , 2008, Brain : a journal of neurology.
[5] Brian B. Avants,et al. Symmetric diffeomorphic image registration with cross-correlation: Evaluating automated labeling of elderly and neurodegenerative brain , 2008, Medical Image Anal..
[6] C. Duijn,et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 , 2006, Nature.
[7] 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.
[8] V. Carey,et al. Mixed-Effects Models in S and S-Plus , 2001 .
[9] C R Jack,et al. Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN , 2009, Neurology.
[10] B. Boeve,et al. Frontotemporal Dementia Treatment: Current Symptomatic Therapies and Implications of Recent Genetic, Biochemical, and Neuroimaging Studies , 2007, Alzheimer disease and associated disorders.
[11] Armando Manduca,et al. Methodological considerations for measuring rates of brain atrophy , 2003, Journal of magnetic resonance imaging : JMRI.
[12] C R Jack,et al. Atrophy patterns in IVS10+16, IVS10+3, N279K, S305N, P301L, and V337M MAPT mutations , 2009, Neurology.
[13] C. Jack,et al. Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics , 2012, Brain : a journal of neurology.
[14] Nick C Fox,et al. Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features , 2012, Alzheimer's & Dementia.
[15] S. Melquist,et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 , 2006, Nature.
[16] J. Gunter,et al. Trajectories of brain and hippocampal atrophy in FTD with mutations in MAPT or GRN , 2011, Neurology.
[17] Clifford R. Jack,et al. Rates of β-amyloid accumulation are independent of hippocampal neurodegeneration , 2014, Neurology.
[18] B. Miller,et al. Classification of primary progressive aphasia and its variants , 2011, Neurology.
[19] Ronald C Petersen,et al. Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease. , 2006, Archives of neurology.
[20] David Heckerman,et al. A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD , 2011, Neuron.
[21] Bruce L. Miller,et al. Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS , 2011, Neuron.
[22] S. Melquist,et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. , 2006, Human molecular genetics.
[23] D. Geschwind,et al. Frontotemporal dementia due to C9ORF72 mutations , 2012, Neurology.
[24] R. Faber,et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. , 1999, Neurology.
[25] Ronald C. Petersen,et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 , 1998, Nature.
[26] M. Folstein,et al. Clinical diagnosis of Alzheimer's disease: Report of the NINCDS—ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease , 2011, Neurology.