M. Barthez-Carpentier

A case of Lennox‐Gastaut syndrome in a patient with FOXG1‐related disorder

C. Delanoé, S. Auvin, D. Germanaud, 2014, Epilepsia.

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

C. Adam, S. Dupont, C. Depienne, 2010, Journal of Medical Genetics.

A case of childhood Kufs' disease.

C. Billard, M. Barthez-Carpentier, M. Ruchoux, 1991, Journal of neurology, neurosurgery, and psychiatry.

Relapse of Herpes Simplex Encephalitis

P. Lebon, F. Rozenberg, M. Tardieu, 1995, Journal of child neurology.

[DRESS syndrome, a drug reaction which remains bad known from paediatricians].

M. Barthez-Carpentier, E. Saliba, L. Bensouda-Grimaldi, 2007, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Cognitive functions in duchenne muscular dystrophy: A reappraisal and comparison with spinal muscular atrophy

J. Signoret, M. Fardeau, C. Billard, 1992, Neuromuscular Disorders.

Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome

C. Adam, S. Dupont, C. Depienne, 2010, Journal of Medical Genetics.