Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images-Reference-Cited by-同舟云学术

Brain atrophy over time in genetic and sporadic frontotemporal dementia: a study of 198 serial magnetic resonance images

Published:2015-02-12 Issue:5 Volume:22 Page:745-752
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Eur J Neurol

Author:

Whitwell J. L.¹,Boeve B. F.²,Weigand S. D.³,Senjem M. L.¹⁴,Gunter J. L.¹⁴,Baker M. C.⁵,DeJesus-Hernandez M.⁵,Knopman D. S.³,Wszolek Z. K.⁶,Petersen R. C.²,Rademakers R.⁵,Jack C. R.¹,Josephs K. A.²

Affiliation:

1. Department of Radiology; Mayo Clinic; Rochester MN USA

2. Department of Neurology; Mayo Clinic; Rochester MN USA

3. Department of Biostatistics; Mayo Clinic; Rochester MN USA

4. Department of Information Technology; Mayo Clinic; Rochester MN USA

5. Department of Neuroscience; Mayo Clinic; Jacksonville FL USA

6. Department of Neurology; Mayo Clinic; Jacksonville FL USA

Funder

National Institutes of Health

Alzheimer's Association

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ene.12675/fullpdf

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3. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21;Cruts;Nature,2006

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5. A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD;Renton;Neuron,2011

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