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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 10, 2009
Sleep disorders in succinic semialdehyde dehydrogenase deficiency: a family reportValentina M Racaru, Jean-Marc Pinard, Fawzia Cheliout-HerautJournal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|January 18, 2006
Protein depletion from blood plasma using a volatile bufferDmitri Sitnikov, Donovan Chan, Eric Thibaudeau, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 20, 2012
Sleep-disordered breathing in children with congenital muscular dystrophiesJean-Marc Pinard, Eric Azabou, Nouha Essid, et al.Neurosurgery|January 18, 2007
Subependymal giant-cell astrocytomas in pediatric tuberous sclerosis disease: when should we operate?Sandrine de Ribaupierre, Georg Dorfmüller, Christine Bulteau, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 14, 2012
Sleep architecture impairment in epileptic children and putative role of anti epileptic drugsValentina M Racaru, Fawzia Cheliout-Heraut, Eric Azabou, et al.Epilepsy & Behavior : E&B|May 16, 2016
Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutationsDelphine Breuillard, Dorothée Leunen, Nicole Chemaly, et al.European Journal of Human Genetics : EJHG|January 12, 2012
Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brotherAnne-Claude Tabet, Marion Pilorge, Richard Delorme, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|December 12, 2018
Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutationNicole Chemaly, Emma Losito, Jean Marc Pinard, et al.Endocrinology|November 5, 2005
Organ messenger ribonucleic acid and plasma proteome changes in the adjuvant-induced arthritis model: responses to disease induction and therapy with the estrogen receptor-beta selective agonist ERB-041Maximillian T Follettie, Marc Pinard, James C Keith, et al.Brain & Development|December 22, 2005
Brain MRI abnormalities in muscular dystrophy due to FKRP mutationsSusana Quijano-Roy, Itxaso Martí-Carrera, Samira Makri, et al.Pageof 3