Area of research
Neurology · Genetics
Research interest
Research interests include Amyotrophic lateral sclerosis, Biology, Medicine, Neurodegeneration, Neuroscience, and Internal medicine.
In‐depth analysis of data from the RAS‐ALS study reveals new insights in rasagiline treatment for amyotrophic lateral sclerosis
Skeletal muscle in amyotrophic lateral sclerosis
Integrative genetic analysis illuminates ALS heritability and identifies risk genes
Loss of hypothalamic MCH decreases food intake in amyotrophic lateral sclerosis
Integrative genetic analyses illuminates ALS heritability and identifies novel risk genes
Integrative genetic analyses illuminates ALS heritability and identifies novel risk genes
Integrative genetic analyses illuminates ALS heritability and identifies novel risk genes
Hypothalamus and weight loss in amyotrophic lateral sclerosis
Effect of high-caloric nutrition on serum neurofilament light chain levels in amyotrophic lateral sclerosis
Effect of High‐Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis
Safety and efficacy of rasagiline as an add-on therapy to riluzole in patients with amyotrophic lateral sclerosis: a randomised, double-blind, parallel-group, placebo-controlled, phase 2 trial
Hypertonic Stress Causes Cytoplasmic Translocation of Neuronal, but Not Astrocytic, FUS due to Impaired Transportin Function
Motor neuron intrinsic and extrinsic mechanisms contribute to the pathogenesis of FUS-associated amyotrophic lateral sclerosis
Could Conservative Iron Chelation Lead to Neuroprotection in Amyotrophic Lateral Sclerosis?© Caroline Moreau <i>et al</i> . 2018; Published by Mary Ann Liebert, Inc. This Open Access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Toxic gain of function from mutant <scp>FUS</scp> protein is crucial to trigger cell autonomous motor neuron loss
Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis
Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis
Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study
Mechanisms, models and biomarkers in amyotrophic lateral sclerosis
VAPB/ALS8 MSP Ligands Regulate Striated Muscle Energy Metabolism Critical for Adult Survival in Caenorhabditis elegans
A Randomized, Double Blind, Placebo-Controlled Trial of Pioglitazone in Combination with Riluzole in Amyotrophic Lateral Sclerosis