Bruno Eymard

Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification.

G. Bassez, D. Hamroun, B. Eymard, 2016, Revue neurologique.

The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease.

F. Chapon, D. Orlikowski, J. Hogrel, 2013, Revue neurologique.

Consensus on cerebral involvement in myotonic dystrophy Workshop report: May 24–27, 2013, Ferrere (AT), Italy

G. Meola, G. Bassez, L. Ranum, 2014, Neuromuscular Disorders.

Late-onset cervicoscapular muscle atrophy and weakness after radiotherapy for Hodgkin disease: a case series

J. Lefaucheur, G. Bassez, B. Eymard, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

Childhood-onset form of myotonic dystrophy type 1 and autism spectrum disorder: Is there comorbidity?

L. Servais, D. Cohen, J. Xavier, 2017, Neuromuscular Disorders.