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Behavioural Neurology|December 18, 2012
Decrease of mutual information in brain electrical activity of patients with relapsing-remitting multiple sclerosisBruno Lenne, Jean-Luc Blanc, Jean-Louis Nandrino, et al.
Multiple Sclerosis International|August 27, 2016
EVASEP: A Noninterventional Study Describing the Perception of Neurologists, Patients, and Caregivers on Caregivers' Role in the Support of Patients Suffering from Multiple Sclerosis Treated with Subcutaneous Interferon Beta 1aCécile Donzé, Bruno Lenne, Anne-Sophie Jean Deleglise, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|June 2, 2026
Temporal perception, attentional bias, and moral reasoning in multiple sclerosis: a moderated mediation analysisLaurent Zikos, Antonio Pinti, Stéphane Ranfaing, et al.
Multiple Sclerosis Journal - Experimental, Translational and Clinical|June 14, 2017
Treatment discontinuation in multiple sclerosis: The French Web-based survey ALLIANCECécile Donzé, Lucie Malapel, Arnaud Kwiatkowski, et al.
Frontiers in Psychology|August 2, 2024
Distinguishing the role of positivity bias, cognitive impairment and emotional reactivity in the deontological preference in multiple sclerosis during moral dilemmas: a social cognition study protocolLaurent Zikos, Béatrice Degraeve, Antonio Pinti, et al.
European Journal of Medical Genetics|December 15, 2010
A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delaySonia Bouquillon, Joris Andrieux, Emilie Landais, et al.
European Journal of Human Genetics : EJHG|December 16, 2018
Holt-Oram syndrome: clinical and molecular description of 78 patients with TBX5 variantsClémence Vanlerberghe, Anne-Sophie Jourdain, Jamal Ghoumid, et al.
Molecular Metabolism|May 23, 2018
CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disabilityLouise Montagne, Mehdi Derhourhi, Amélie Piton, et al.
Human Mutation|May 27, 2015
Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental RetardationLaura Addis, Joo Wook Ahn, Richard Dobson, et al.
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