A. Lacour

Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7

Asma Ammar, François Petit, Nektaria Alexandri et al. · Journal of Neurology · 2009 · 78 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

Acute aphasia in multiple sclerosis

A. Lacour, J. de Sèze, E. Revenco et al. · Neurology · 2004 · 66 citations

Neuropsychology, Ms Patients, Acute Aphasia +15

Relapsing demyelinating disease affecting both the central and peripheral nervous systems

Hélène Zéphir, Tanya Stojkovic, Philippe Latour et al. · Journal of Neurology Neurosurgery & Psychiatry · 2008 · 58 citations

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

Pascal Laforêt, K. Laloui, Benjamin Granger et al. · Revue Neurologique · 2013 · 57 citations

Adult Pompe Disease, Global Health, Clinical Epidemiology +5

Central nervous system abnormalities in patients with PMP22 gene mutations: a prospective study

Jean‐Baptiste Chanson, Andoni Echaniz‐Laguna, Frédéric Blanc et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 42 citations