H. Isnard

Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature

I. Scheffer, H. Mefford, A. Munnich, 2019, Human mutation.

[Generalized idiopathic epilepsy in older children and adolescents].

C. Berger, N. Badinand-Hubert, M. Revol, 1994, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Benign Myoclonic Epilepsy in Infants: Electroclinical Features and Long‐term Follow‐up of 34 Patients

L. Vallée, S. Auvin, J. Motte, 2006, Epilepsia.

Developmental and epilepsy spectrum of KCNB1 encephalopathy with long‐term outcome

I. Scheffer, H. Mefford, A. Munnich, 2020, Epilepsia.

Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy

Anne de Saint Martin, A. Afenjar, P. Berquin, 2021, Epilepsy & Behavior.

ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate

S. Rheims, P. Berquin, S. Auvin, 2016, Epilepsia.

[Transitory EEG asymmetry at the start of quiet sleep in the newborn infant: 75 cases].

A. Brunon, M. Challamel, H. Isnard, 1984, Revue d'electroencephalographie et de neurophysiologie clinique.

Progressive Facial Hemiatrophy with Multiple Benign Tumors and Hamartomas

L. Derex, M. Revol, H. Isnard, 1995, Neuropediatrics.

Human Mutation

Anne de Saint Martin, I. Scheffer, H. Mefford, 2019 .