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Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|February 12, 2021
Increased worsening of amyotrophic lateral sclerosis patients during Covid-19-related lockdown in FranceFlorence Esselin, Elisa De La Cruz, Nicolas Pageot, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|November 26, 2021
Reversible sub-acute motor neuron syndrome after mushroom intoxication masquerading as amyotrophic lateral sclerosisEmmeline Lagrange, Elisa de la Cruz, Florence Esselin, et al.CNS Neuroscience & Therapeutics|June 25, 2022
Repeated neurofilament light chain measurements did not capture Riluzole therapeutic effect in amyotrophic lateral sclerosis patientsFlorence Esselin, Elisa De la Cruz, Christophe Hirtz, et al.Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|October 20, 2021
Compound heterozygous P67S/D91A SOD1 mutations in an ALS family with apparently sporadic caseElisa De La Cruz, Claire Guissart, Florence Esselin, et al.Frontiers in Neurology|June 18, 2020
Low 25OH Vitamin D Blood Levels Are Independently Associated With Higher Amyotrophic Lateral Sclerosis Severity Scores: Results From a Prospective StudyRaul Juntas-Morales, Nicolas Pageot, Gregory Marin, et al.Journal of Neurology|April 18, 2026
Correlations between peripheral neuropathy profiles and vascular skin lesionsMorgan Dornadic, Didier Bessis, Florence Esselin, et al.Bioanalysis|August 31, 2023
Ultrasensitive digital immunoassays for SOD1 conformation in amyotrophic lateral sclerosisLisa Morichon, Christophe Hirtz, Laurent Tiers, et al.European Journal of Neurology|April 8, 2023
Serum neurofilament light chain cut-off definition for clinical diagnosis and prognosis of amyotrophic lateral sclerosisMehdi Brousse, Constance Delaby, Elisa De La Cruz, et al.Stem Cell Research|August 30, 2025
Generation of three iPSC lines from patients with CACNA1S related congenital myopathyReem Bou Akar, Karine Giraud-Triboult, Lina El Kassar, et al.International Journal of Molecular Sciences|April 27, 2024
The Hexokinase 1 5'-UTR Mutation in Charcot-Marie-Tooth 4G Disease Alters Hexokinase 1 Binding to Voltage-Dependent Anion Channel-1 and Leads to Dysfunctional Mitochondrial Calcium BufferingMaria Ceprian, Raul Juntas-Morales, Graham Campbell, et al.Pageof 3