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F Andermann

Showing results (361-370 of 367) with videos related to

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Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, 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.
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.
Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, 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.
Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Pageof 37

Showing results (361-370 of 367) with videos related to

Sort By:
Pageof 37
You have reached the last page of results.This site can display upto 367 results.
Epilepsy Research|March 27, 1999
Congenital malformations due to antiepileptic drugsS Kaneko, D Battino, E Andermann, 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.
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.
Annals of Neurology|July 14, 2000
Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopmentM M Guerreiro, E Andermann, R Guerrini, 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.
Human Molecular Genetics|September 5, 2001
Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in femalesV L Sheen, P H Dixon, J W Fox, et al.
Neurology|January 26, 2005
Filamin A mutations cause periventricular heterotopia with Ehlers-Danlos syndromeV L Sheen, A Jansen, M H Chen, et al.
Pageof 37