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Isabelle Le Ber

Showing results (41-50 of 211) with videos related to

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JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
Neurobiology of Aging|June 10, 2014
Homozygous TREM2 mutation in a family with atypical frontotemporal dementiaIsabelle Le Ber, Anne De Septenville, Rita Guerreiro, et al.
Journal of Alzheimer'S Disease : JAD|August 17, 2013
Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389RMarie-Pierre Chaunu, Vincent Deramecourt, Valérie Buée-Scherrer, et al.
Brain : a Journal of Neurology|February 16, 2013
C9orf72 repeat expansions are a rare genetic cause of parkinsonismSuzanne Lesage, Isabelle Le Ber, Christel Condroyer, et al.
Scientific Reports|March 3, 2018
Author Correction: Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substratesFernando Bartolome, Noemi Esteras, Angeles Martin-Requero, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Neurobiology of Aging|August 16, 2020
Does amnesia specifically predict Alzheimer's pathology? A neuropathological studyMaxime Bertoux, Pascaline Cassagnaud, Thibaud Lebouvier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 26, 2018
Neurite density is reduced in the presymptomatic phase of <i>C9orf72</i> diseaseJunhao Wen, Hui Zhang, Daniel C Alexander, et al.
Neurobiology of Aging|October 15, 2013
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypesIsabelle Le Ber, Inge Van Bortel, Gael Nicolas, et al.
Archives of Neurology|April 11, 2007
Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-upPascale Ribaï, Françoise Pousset, Marie-Laure Tanguy, et al.
Pageof 22

Showing results (41-50 of 211) with videos related to

Sort By:
Pageof 22
JAMA Neurology|October 16, 2014
Extensive white matter involvement in patients with frontotemporal lobar degeneration: think progranulinPaola Caroppo, Isabelle Le Ber, Agnès Camuzat, et al.
Neurobiology of Aging|June 10, 2014
Homozygous TREM2 mutation in a family with atypical frontotemporal dementiaIsabelle Le Ber, Anne De Septenville, Rita Guerreiro, et al.
Journal of Alzheimer'S Disease : JAD|August 17, 2013
Juvenile frontotemporal dementia with parkinsonism associated with tau mutation G389RMarie-Pierre Chaunu, Vincent Deramecourt, Valérie Buée-Scherrer, et al.
Brain : a Journal of Neurology|February 16, 2013
C9orf72 repeat expansions are a rare genetic cause of parkinsonismSuzanne Lesage, Isabelle Le Ber, Christel Condroyer, et al.
Scientific Reports|March 3, 2018
Author Correction: Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substratesFernando Bartolome, Noemi Esteras, Angeles Martin-Requero, et al.
Neurobiology of Aging|August 27, 2014
Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patientsAnnabelle Chaussenot, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.
Neurobiology of Aging|August 16, 2020
Does amnesia specifically predict Alzheimer's pathology? A neuropathological studyMaxime Bertoux, Pascaline Cassagnaud, Thibaud Lebouvier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 26, 2018
Neurite density is reduced in the presymptomatic phase of <i>C9orf72</i> diseaseJunhao Wen, Hui Zhang, Daniel C Alexander, et al.
Neurobiology of Aging|October 15, 2013
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypesIsabelle Le Ber, Inge Van Bortel, Gael Nicolas, et al.
Archives of Neurology|April 11, 2007
Neurological, cardiological, and oculomotor progression in 104 patients with Friedreich ataxia during long-term follow-upPascale Ribaï, Françoise Pousset, Marie-Laure Tanguy, et al.
Pageof 22