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Neurology|July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancyP Striano, A Coppola, M Pezzella, et al.Molecular Psychiatry|July 9, 2008
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1L Palmieri, V Papaleo, V Porcelli, et al.The Journal of Nutrition, Health & Aging|February 23, 2007
IANA (International Academy on Nutrition and Aging) Expert Group: weight loss and Alzheimer's diseaseS Gillette Guyonnet, G Abellan Van Kan, E Alix, et al.European Journal of Neurology|October 2, 2012
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolutionS Agostinelli, M Traverso, P Accorsi, et al.The Journal of Nutrition, Health & Aging|September 24, 2008
Prevention of progression to dementia in the elderly: rationale and proposal for a health-promoting memory consultation (an IANA Task Force)S Gillette Guyonnet, G Abellan Van Kan, S Andrieu, et al.Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.European Journal of Neurology|October 10, 2018
Management of psychogenic non-epileptic seizures: a multidisciplinary approachS Gasparini, E Beghi, E Ferlazzo, et al.Reumatologia Clinica|March 12, 2013
Different clinical expression of patients with ankylosing spondylitis according to gender in relation to time since onset of disease. Data from REGISPONSERRafaela Ortega Castro, Pilar Font Ugalde, M Carmen Castro Villegas, et al.Journal of Medical Genetics|April 18, 2009
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeB W M van Bon, H C Mefford, B Menten, et al.Pageof 59