The Heritability of Frontotemporal Lobar Degeneration: Validation of Pedigree Classification Criteria in a Northern Italy Cohort
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Title
The Heritability of Frontotemporal Lobar Degeneration: Validation of Pedigree Classification Criteria in a Northern Italy Cohort
Authors
Keywords
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Journal
JOURNAL OF ALZHEIMERS DISEASE
Volume 61, Issue 2, Pages 753-760
Publisher
IOS Press
Online
2017-12-09
DOI
10.3233/jad-170661
References
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Note: Only part of the references are listed.- Genetic Counseling and Testing for Alzheimer’s Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol
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- (2013) Clement T Loy et al. LANCET
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- (2013) Elisabeth M. Wood et al. JAMA Neurology
- A Pan-European Study of theC9orf72Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats
- (2012) Julie van der Zee et al. HUMAN MUTATION
- Motor Neuron dysfunction in frontotemporal dementia
- (2011) James R. Burrell et al. BRAIN
- Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
- (2011) Katya Rascovsky et al. BRAIN
- Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study
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- The heritability and genetics of frontotemporal lobar degeneration
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- Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide
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- Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
- (2008) R. Ghidoni et al. NEUROLOGY
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