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Anne de Septenville

Showing results (11-20 of 15) with videos related to

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Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Neurobiology of Aging|October 18, 2015
TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohortsIsabelle Le Ber, Anne De Septenville, Stéphanie Millecamps, 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.
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.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Neurogenetics|January 29, 2014
Partial deletions of the GRN gene are a cause of frontotemporal lobar degenerationFabienne Clot, Anne Rovelet-Lecrux, Foudil Lamari, et al.
Neurobiology of Aging|October 18, 2015
TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohortsIsabelle Le Ber, Anne De Septenville, Stéphanie Millecamps, 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.
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.
Brain : a Journal of Neurology|June 18, 2014
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementSylvie Bannwarth, Samira Ait-El-Mkadem, Annabelle Chaussenot, et al.
Pageof 2