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C BRUNI

Showing results (141-150 of 152) with videos related to

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Neurobiology of Aging|December 8, 2019
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's diseaseIrene Rosas, Carmen Martínez, Jordi Clarimón, et al.
Nature|June 29, 1995
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's diseaseR Sherrington, E I Rogaev, Y Liang, et al.
Nature|September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorderP H St George-Hyslop, J L Haines, L A Farrer, et al.
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.
Pageof 16

Showing results (141-150 of 152) with videos related to

Sort By:
Pageof 16
Neurobiology of Aging|December 8, 2019
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's diseaseIrene Rosas, Carmen Martínez, Jordi Clarimón, et al.
Nature|June 29, 1995
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's diseaseR Sherrington, E I Rogaev, Y Liang, et al.
Nature|September 13, 1990
Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorderP H St George-Hyslop, J L Haines, L A Farrer, et al.
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.
Pageof 16