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Isabelle Le Ber

Showing results (121-130 of 211) with videos related to

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Neurobiology of Aging|March 16, 2020
Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experienceLeila Sellami, Benoît Rucheton, Imen Ben Younes, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
Nature Medicine|May 14, 2024
Progranulin AAV gene therapy for frontotemporal dementia: translational studies and phase 1/2 trial interim resultsJeffrey Sevigny, Olga Uspenskaya, Laura Dean Heckman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 6, 2021
Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohortGeorgia Peakman, Lucy L Russell, Rhian S Convery, et al.
Journal of Neurology|November 28, 2022
Loss of brainstem white matter predicts onset and motor neuron symptoms in C9orf72 expansion carriers: a GENFI studyAgnès Pérez-Millan, Sergi Borrego-Écija, John C van Swieten, et al.
JAMA Network Open|September 24, 2021
Effect of the Histone Deacetylase Inhibitor FRM-0334 on Progranulin Levels in Patients With Progranulin Gene Haploinsufficiency: A Randomized Clinical TrialPeter A Ljubenkov, Lauren Edwards, Leonardo Iaccarino, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Nature Genetics|February 11, 2004
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2Maria-Céu Moreira, Sandra Klur, Mitsunori Watanabe, et al.
Neurology. Genetics|July 24, 2025
Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI StudyLucy Louise Russell, Arabella Bouzigues, Rhian S Convery, et al.
JAMA Neurology|February 27, 2018
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia GenesMarie Coutelier, Monia B Hammer, Giovanni Stevanin, et al.
Pageof 22

Showing results (121-130 of 211) with videos related to

Sort By:
Pageof 22
Neurobiology of Aging|March 16, 2020
Plasma progranulin levels for frontotemporal dementia in clinical practice: a 10-year French experienceLeila Sellami, Benoît Rucheton, Imen Ben Younes, et al.
Brain : a Journal of Neurology|September 26, 2013
Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, Camille Charbonnier, et al.
Nature Medicine|May 14, 2024
Progranulin AAV gene therapy for frontotemporal dementia: translational studies and phase 1/2 trial interim resultsJeffrey Sevigny, Olga Uspenskaya, Laura Dean Heckman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 6, 2021
Comparison of clinical rating scales in genetic frontotemporal dementia within the GENFI cohortGeorgia Peakman, Lucy L Russell, Rhian S Convery, et al.
Journal of Neurology|November 28, 2022
Loss of brainstem white matter predicts onset and motor neuron symptoms in C9orf72 expansion carriers: a GENFI studyAgnès Pérez-Millan, Sergi Borrego-Écija, John C van Swieten, et al.
JAMA Network Open|September 24, 2021
Effect of the Histone Deacetylase Inhibitor FRM-0334 on Progranulin Levels in Patients With Progranulin Gene Haploinsufficiency: A Randomized Clinical TrialPeter A Ljubenkov, Lauren Edwards, Leonardo Iaccarino, et al.
Annals of Clinical and Translational Neurology|August 11, 2022
The CBI-R detects early behavioural impairment in genetic frontotemporal dementiaAnnabel Nelson, Lucy L Russell, Georgia Peakman, et al.
Nature Genetics|February 11, 2004
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2Maria-Céu Moreira, Sandra Klur, Mitsunori Watanabe, et al.
Neurology. Genetics|July 24, 2025
Executive Function Deficits in Genetic Frontotemporal Dementia: Results From the GENFI StudyLucy Louise Russell, Arabella Bouzigues, Rhian S Convery, et al.
JAMA Neurology|February 27, 2018
Efficacy of Exome-Targeted Capture Sequencing to Detect Mutations in Known Cerebellar Ataxia GenesMarie Coutelier, Monia B Hammer, Giovanni Stevanin, et al.
Pageof 22