Domitille Gras

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 · 126 citations

Life Sciences, Genetics, Molecular Genetics +17

<i>ADCY5</i> -related dyskinesia

Donghui Chen, Aurélie Méneret, Jennifer Friedman et al. · Neurology · 2015 · 119 citations · Full text

Life Sciences, Genetics, Neurology +13

<i>PRRT2</i> mutations

Aurélie Méneret, David Grabli, Christel Depienne et al. · Neurology · 2012 · 106 citations

Life Sciences, Genetics, Molecular Genetics +16

Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2

Mathieu Milh, Nadia Boutry‐Kryza, Julie Sutera-Sardo et al. · Orphanet Journal of Rare Diseases · 2013 · 92 citations · Full text

Medicine, Genetics, Neurology +17

Triheptanoin dramatically reduces paroxysmal motor disorder in patients with GLUT1 deficiency

Fanny Mochel, Élodie Hainque, Domitille Gras et al. · Journal of Neurology Neurosurgery & Psychiatry · 2015 · 90 citations · Full text

Medicine, Neurology, Pharmacology +14