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American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.Epilepsia|October 3, 2001
Surgical resection for intractable epilepsy in "double cortex" syndrome yields inadequate resultsA Bernasconi, V Martinez, P Rosa-Neto, et al.Human Molecular Genetics|March 21, 1998
Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic depositsH M Mitchison, S L Hofmann, C H Becerra, et al.Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, et al.Nature Genetics|March 1, 1997
Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1R G Lafrenière, D L Rochefort, N Chrétien, et al.Physical Review Letters|April 6, 2001
Precise half-life measurement for the superallowed 0(+)-->0(+) beta emitter (74)Rb: first results from the new radioactive beam facility (ISAC) at TRIUMFG C Ball, S Bishop, J A Behr, et al.Physical Review Letters|February 3, 2004
Determination of the 8B neutrino spectrumW T Winter, S J Freedman, K E Rehm, et al.Epilepsy Research|August 27, 1999
Intrauterine growth in the offspring of epileptic women: a prospective multicenter studyD Battino, S Kaneko, E Andermann, et al.Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, et al.Pageof 34