E. Caietta

Cerebral 18FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-d-aspartate receptor encephalitis: A case series

E. Guedj, M. Milh, S. Lagarde, 2016, Brain and Development.

Large in-frame intragenic deletion of OPHN1 in a male patient with a normal intelligence quotient score

N. Philip, N. Girard, B. Chabrol, 2017, Clinical dysmorphology.

Recurrent mutations in the CDKL5 gene: Genotype–phenotype relationships

H. Van Esch, G. Matthijs, T. Bienvenu, 2012, American journal of medical genetics. Part A.

Diagnosis and Outcome of SCN4A-Related Severe Neonatal Episodic Laryngospasm (SNEL): 2 New Cases

A. McGonigal, M. Milh, D. Sternberg, 2013, Pediatrics.

Primary Leptomeningeal Gliomatosis in Children and Adults: A Morphological and Molecular Comparative Study With Literature Review.

P. Varlet, J. Grill, A. Laquérriere, 2016, Neurosurgery.

Cerebral 18FluoroDeoxy-Glucose Positron Emission Tomography in paediatric anti N-methyl-d-aspartate receptor encephalitis: A case series

E. Guedj, M. Milh, S. Lagarde, 2016, Brain and Development.