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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.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.Annales De Genetique|May 26, 1998
A gene for non-specific X-linked mental retardation (MRX55) is located in Xp11S C Deqaqi, M N'Guessan, J Forner, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Type 2 neurofibromatosis: intergenerational differences in genetic and clinical expression]A Drouet, F Le Moigne, D Salamé, et al.American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.American Journal of Medical Genetics|July 9, 1999
Refined 2.7 centimorgan locus in Xp21.3-22.1 for a nonspecific X-linked mental retardation gene (MRX54)L B Jemaa, V des Portes, R Zemni, et al.Pageof 5