A. Le Moing

Molecular characterization of a cohort of 73 patients with infantile spasms syndrome.

R. Touraine, E. Bourel-ponchel, D. Ville, 2015, European journal of medical genetics.

Phenotype–genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature

E. Bourel-ponchel, C. Rooryck, D. Lacombe, 2015, American journal of medical genetics. Part A.

Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy

L. Servais, J. Hogrel, P. Carlier, 2016, Neurology.

Upper Limb Strength and Function Changes during a One-Year Follow-Up in Non-Ambulant Patients with Duchenne Muscular Dystrophy: An Observational Multicenter Trial

L. Servais, J. Hogrel, S. Quijano-roy, 2015, PloS one.

Effects of Methylphenidate on Default-Mode Network/Task-Positive Network Synchronization in Children With ADHD

M. Boucart, C. Gondry-Jouet, P. Berquin, 2017, Journal of attention disorders.

Should isolated fetal ventriculomegaly measured below 12 mm be viewed as a variant of the norm? Results of a 5-year experience in a prenatal referral center

P. Tourneux, C. Gondry-Jouet, J. Gondry, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype

L. Servais, J. Hogrel, F. Leturcq, 2015, Journal of neuromuscular diseases.

Prospective follow-up of a cohort of preterm infants<33 WG receiving ketamine for tracheal intubation in the delivery room: Neurological outcome at 1 and 2 years.

P. Tourneux, A. Léké, G. Kongolo, 2018, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

EML1‐associated brain overgrowth syndrome with ribbon‐like heterotopia

M. Lequin, G. Mancini, S. Mandelstam, 2019, American journal of medical genetics. Part C, Seminars in medical genetics.

A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment

Thomas Voit, David Vissière, Jean-Yves Hogrel, 2016, PloS one.

Kleefstra syndrome: Recurrence in siblings due to a paternal mosaic mutation

A. Piton, M. Mathieu-Dramard, A. Le Moing, 2021, American journal of medical genetics. Part A.

[Familial and non-familial benign infantile seizures: A homogeneous entity?].

F. Wallois, P. Berquin, A. Delignières, 2011, Revue neurologique (Paris).

Contribution of Whole-Genome Sequencing and Transcript Analysis to Decipher Retinal Diseases Associated with MFSD8 Variants

H. Dollfus, D. Schorderet, M. Todorova, 2022, International journal of molecular sciences.

Upper Limb Evaluation and One-Year Follow Up of Non-Ambulant Patients with Spinal Muscular Atrophy: An Observational Multicenter Trial

L. Servais, J. Hogrel, S. Quijano-roy, 2015, PloS one.

Maturation of response time and attentional control in ADHD: evidence from an attentional capture paradigm.

P. Berquin, L. Querné, A. Delignières, 2011, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Vagus nerve stimulation in the treatment of drug-resistant epilepsy in 29 children.

P. Berquin, L. Querné, P. Toussaint, 2016, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.