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Isabelle Le Ber

Showing results (71-80 of 211) with videos related to

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Neurobiology of Aging|October 20, 2018
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriersClémence Fournier, Mathieu Barbier, Agnès Camuzat, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|April 14, 2021
Frontotemporal dementia subtypes based on behavioral inhibition deficitsValérie Godefroy, Delphine Tanguy, Arabella Bouzigues, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 31, 2016
Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriersPaola Caroppo, Agnès Camuzat, Anne De Septenville, et al.
Acta Neuropathologica Communications|July 21, 2016
Reduced Tau protein expression is associated with frontotemporal degeneration with progranulin mutationAnthony Papegaey, Sabiha Eddarkaoui, Vincent Deramecourt, et al.
JAMA Neurology|September 18, 2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosisIsabelle Le Ber, Agnès Camuzat, Rita Guerreiro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 26, 2020
Plasma microRNA signature in presymptomatic and symptomatic subjects with <i>C9orf72</i>-associated frontotemporal dementia and amyotrophic lateral sclerosisVirgilio Kmetzsch, Vincent Anquetil, Dario Saracino, et al.
European Journal of Human Genetics : EJHG|June 2, 2016
Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencingStéphanie David, Joana Ferreira, Olivier Quenez, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Nature Neuroscience|July 25, 2022
Neurovascular dysfunction in GRN-associated frontotemporal dementia identified by single-nucleus RNA sequencing of human cerebral cortexEmma Gerrits, Lucia A A Giannini, Nieske Brouwer, et al.
Archives of Neurology|April 12, 2012
Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegiaSophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, et al.
Pageof 22

Showing results (71-80 of 211) with videos related to

Sort By:
Pageof 22
Neurobiology of Aging|October 20, 2018
Relations between C9orf72 expansion size in blood, age at onset, age at collection and transmission across generations in patients and presymptomatic carriersClémence Fournier, Mathieu Barbier, Agnès Camuzat, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|April 14, 2021
Frontotemporal dementia subtypes based on behavioral inhibition deficitsValérie Godefroy, Delphine Tanguy, Arabella Bouzigues, et al.
Alzheimer'S & Dementia (Amsterdam, Netherlands)|May 31, 2016
Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriersPaola Caroppo, Agnès Camuzat, Anne De Septenville, et al.
Acta Neuropathologica Communications|July 21, 2016
Reduced Tau protein expression is associated with frontotemporal degeneration with progranulin mutationAnthony Papegaey, Sabiha Eddarkaoui, Vincent Deramecourt, et al.
JAMA Neurology|September 18, 2013
SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosisIsabelle Le Ber, Agnès Camuzat, Rita Guerreiro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 26, 2020
Plasma microRNA signature in presymptomatic and symptomatic subjects with <i>C9orf72</i>-associated frontotemporal dementia and amyotrophic lateral sclerosisVirgilio Kmetzsch, Vincent Anquetil, Dario Saracino, et al.
European Journal of Human Genetics : EJHG|June 2, 2016
Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencingStéphanie David, Joana Ferreira, Olivier Quenez, et al.
Annals of Neurology|April 8, 2009
TARDBP mutations in motoneuron disease with frontotemporal lobar degenerationLina Benajiba, Isabelle Le Ber, Agnès Camuzat, et al.
Nature Neuroscience|July 25, 2022
Neurovascular dysfunction in GRN-associated frontotemporal dementia identified by single-nucleus RNA sequencing of human cerebral cortexEmma Gerrits, Lucia A A Giannini, Nieske Brouwer, et al.
Archives of Neurology|April 12, 2012
Factors influencing disease progression in autosomal dominant cerebellar ataxia and spastic paraplegiaSophie Tezenas du Montcel, Perrine Charles, Cyril Goizet, et al.
Pageof 22