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Showing results (41-50 of 47) with videos related to

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Acta Neuropathologica|March 9, 2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementiaJennifer S Yokoyama, Celeste M Karch, Chun C Fan, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
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Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Acta Neuropathologica|March 9, 2017
Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementiaJennifer S Yokoyama, Celeste M Karch, Chun C Fan, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Brain : a Journal of Neurology|September 26, 2018
A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriersMing Zhang, Raffaele Ferrari, Maria Carmela Tartaglia, et al.
Neurology|September 18, 2020
<i>C9orf72</i>, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohortsBeatrice Costa, Claudia Manzoni, Manuel Bernal-Quiros, et al.
The Lancet. Neurology|May 5, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association studyCyril Pottier, Xiaolai Zhou, Ralph B Perkerson, et al.
American Journal of Human Genetics|June 18, 2024
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementiaClaudia Manzoni, Demis A Kia, Raffaele Ferrari, et al.
The Lancet. Neurology|June 20, 2014
Frontotemporal dementia and its subtypes: a genome-wide association studyRaffaele Ferrari, Dena G Hernandez, Michael A Nalls, et al.
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