Cortical degeneration in frontotemporal lobar degeneration with TDP-43 proteinopathy caused byprogranulingene mutation
Author:
Publisher
Informa UK Limited
Subject
General Medicine,General Neuroscience
Link
http://www.tandfonline.com/doi/pdf/10.3109/00207454.2014.890620
Reference44 articles.
1. Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration
2. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
3. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
4. HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin
5. Neuropathologic Heterogeneity in HDDD1: A Familial Frontotemporal Lobar Degeneration With Ubiquitin-positive Inclusions and Progranulin Mutation
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1. What causes neurodegenerative disease?;Folia Neuropathologica;2020
2. A Possible Explanation For Neurodegenerative Disease;EMJ Neurology;2019-08-13
3. Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease;Brain;2017-08-18
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