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Revue Neurologique|November 26, 2013
GLUT1 deficiency syndrome: an updateD Gras, E Roze, S Caillet, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 20, 2007
[Human herpes virus type 6, etiology of an acute encephalitis in childhood: case report]A Afenjar, D Rodriguez, F Rozenberg, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 3, 2004
[Management of acute visual loss in children]D Doummar, B Roussat, B Pelosse, et al.
Revue Neurologique|September 1, 2018
Monoamine neurotransmitters and movement disorders in children and adultsD Doummar, F Moussa, M-C Nougues, et al.
Journal Francais D'Ophtalmologie|March 10, 2001
[Acute optic neuritis in children: clinical features and treatment. A study of 28 eyes in 20 children]B Roussat, P Gohier, D Doummar, et al.
American Journal of Medical Genetics. Part A|September 27, 2014
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formationJ Milosevic, L El Khattabi, A Roubergue, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|August 31, 2015
Advances in the metabolic profiling of acidic compounds in children's urines achieved by comprehensive two-dimensional gas chromatographyN Pérez Vasquez, M Crosnier de Bellaistre-Bonose, N Lévêque, et al.
Journal of Medical Genetics|October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromesS Tezenas du Montcel, F Clot, M Vidailhet, et al.
Neurology|March 26, 2008
Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutationsE Roze, E Apartis, F Clot, et al.
Clinical Genetics|July 15, 2017
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patientsE Chérot, B Keren, C Dubourg, et al.
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