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C Bruni

Showing results (191-200 of 199) with videos related to

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Biological Psychiatry|March 12, 2013
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentationDaniela Galimberti, Chiara Fenoglio, Maria Serpente, et al.
Neurobiology of Aging|September 25, 2020
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementiaIrene Rosas, Carmen Martínez, Eliecer Coto, et al.
JAMA Neurology|July 19, 2021
Global Prevalence of Young-Onset Dementia: A Systematic Review and Meta-analysisStevie Hendriks, Kirsten Peetoom, Christian Bakker, et al.
Brain : a Journal of Neurology|October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degenerationMathieu Barbier, Agnès Camuzat, Khalid El Hachimi, 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.
Pageof 20

Showing results (191-200 of 199) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 199 results.
Biological Psychiatry|March 12, 2013
Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentationDaniela Galimberti, Chiara Fenoglio, Maria Serpente, et al.
Neurobiology of Aging|September 25, 2020
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementiaIrene Rosas, Carmen Martínez, Eliecer Coto, et al.
JAMA Neurology|July 19, 2021
Global Prevalence of Young-Onset Dementia: A Systematic Review and Meta-analysisStevie Hendriks, Kirsten Peetoom, Christian Bakker, et al.
Brain : a Journal of Neurology|October 23, 2021
SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degenerationMathieu Barbier, Agnès Camuzat, Khalid El Hachimi, 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.
Pageof 20