N. Essid

A de novo 10p11.23‐p12.1 deletion recapitulates the phenotype observed in WAC mutations and strengthens the role of WAC in intellectual disability and behavior disorders

L. E. El Khattabi, J. Dupont, G. Viot, 2016, American journal of medical genetics. Part A.

A simple blood test expedites the diagnosis of glucose transporter type 1 deficiency syndrome

S. Auvin, L. D. Da Costa, O. Boespflug-Tanguy, 2017, Annals of neurology.

Sleep-disordered breathing in children with congenital muscular dystrophies.

S. Quijano-roy, E. Azabou, J. Pinard, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency Syndrome

M. Sitbon, O. Boespflug-Tanguy, F. Mochel, 2023, Neurology.

Sleep architecture impairment in epileptic children and putative role of anti epileptic drugs

E. Azabou, J. Pinard, F. Chéliout-Héraut, 2012, Neurological Sciences.