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Revue Neurologique|April 1, 2005
[Creatine deficiency syndromes]D Cheillan, S Cognat, N Vandenberghe, et al.Neuropediatrics|December 19, 2009
Neurological outcome and risk of recurrence depending on the anterior vs. posterior arterial distribution in children with strokeA Touré, S Chabrier, M D Plagne, et al.American Journal of Medical Genetics|August 18, 2000
Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardationT Bienvenu, V des Portes, N McDonell, et al.Nature|May 15, 1998
Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.Human Molecular Genetics|July 21, 1998
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitorT Bienvenu, V des Portes, A Saint Martin, et al.Neurology|July 23, 2003
Herpes simplex encephalitis relapses in children: differentiation of two neurologic entitiesX De Tiège, F Rozenberg, V Des Portes, et al.European Journal of Medical Genetics|October 10, 2022
STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genesZ Gokce-Samar, J de Bellescize, A Arzimanoglou, et al.Neuropediatrics|August 12, 2003
Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defectsN Deconinck, T Duprez, V des Portes, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 21, 2012
[Diagnosis and care of Wilson disease with neurological revelation]S Wagner, A-S Brunet, M Bost, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 25, 2007
[Acute hemiparesis revealing a neuroborreliosis in a child]C Rénard, S Marignier, Y Gillet, et al.Pageof 11