M. Bru

Health-Related Quality of Life for Children and Adolescents with Specific Language Impairment: A Cohort Study by a Learning Disabilities Reference Center

A. Roy, Gaëlle Hubert‐Dibon, M. Bru, 2016, PloS one.

Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females

F. Rivier, C. Depienne, P. Berquin, 2011, Human mutation.

Delineation of cryptogenic Lennox–Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis

G. Dellatolas, O. Dulac, A. Kaminska, 1999, Epilepsy Research.

Baseline Characteristics of a National French E-Cohort of Hidradenitis Suppurativa in ComPaRe and Comparison with Other Large Hidradenitis Suppurativa Cohorts

P. Ravaud, M. Richard, A. Nassif, 2021, Dermatology.

Praxis skills and executive function in children with neurofibromatosis type 1

D. Le Gall, Chrystelle Remigereau, A. Roy, 2018, Applied neuropsychology. Child.