Laurence Lion‐François

Phenotype and genotype in 101 males with X-linked creatine transporter deficiency

Jiddeke M. van de Kamp, Ofir T. Betsalel, Saadet Mercimek‐Mahmutoglu et al. · Journal of Medical Genetics · 2013 · 159 citations · Full text

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene

Domitille Gras, Laurence Jonard, Emmanuel Roze et al. · Journal of Neurology Neurosurgery & Psychiatry · 2012 · 124 citations

High frequency of creatine deficiency syndromes in patients with unexplained mental retardation

Laurence Lion‐François, David Cheillan, G. Pitelet et al. · Neurology · 2006 · 100 citations

Systematic MRI in NF1 children under six years of age for the diagnosis of optic pathway gliomas. Study and outcome of a French cohort

Gaëlle Blanchard, Marie-Pierre Lafforgue, Laurence Lion‐François et al. · European Journal of Paediatric Neurology · 2015 · 79 citations · Full text

Neuro-oncology, Pediatric Brain Tumors, Optic Pathway Gliomas +10

Liver transplantation as a rescue therapy for severe neurologic forms of Wilson disease

Aurélia Poujois, Rodolphe Sobesky, Wassilios G. Meissner et al. · Neurology · 2020 · 61 citations