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I E Scheffer

Showing results (51-60 of 75) with videos related to

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Pediatric Radiology|December 2, 2000
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findingsT Y Poussaint, J W Fox, W B Dobyns, et al.
AJNR. American Journal of Neuroradiology|January 26, 2013
Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalitiesS A Mandelstam, R J Leventer, A Sandow, et al.
Epilepsia|August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?R Singh, E Andermann, W P Whitehouse, et al.
Neuropediatrics|June 21, 2001
Near-total absence of the cerebellumR J Gardner, L T Coleman, L A Mitchell, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Neurology|April 27, 2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutationsL M Dibbens, R Kneen, M A Bayly, et al.
Brain : a Journal of Neurology|April 8, 2004
Longitudinal study of MRS metabolites in Rasmussen encephalitisR M Wellard, R S Briellmann, J C Wilson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 31, 2000
Phenotypic characterization of an alpha 4 neuronal nicotinic acetylcholine receptor subunit knock-out mouseS A Ross, J Y Wong, J J Clifford, et al.
AJNR. American Journal of Neuroradiology|October 13, 2022
Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim SyndromeB J Halliday, G Baynam, L Ewans, et al.
Nature Genetics|April 28, 2001
Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizuresR H Wallace, C Marini, S Petrou, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Pediatric Radiology|December 2, 2000
Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findingsT Y Poussaint, J W Fox, W B Dobyns, et al.
AJNR. American Journal of Neuroradiology|January 26, 2013
Bilateral posterior periventricular nodular heterotopia: a recognizable cortical malformation with a spectrum of associated brain abnormalitiesS A Mandelstam, R J Leventer, A Sandow, et al.
Epilepsia|August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?R Singh, E Andermann, W P Whitehouse, et al.
Neuropediatrics|June 21, 2001
Near-total absence of the cerebellumR J Gardner, L T Coleman, L A Mitchell, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Neurology|April 27, 2011
Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutationsL M Dibbens, R Kneen, M A Bayly, et al.
Brain : a Journal of Neurology|April 8, 2004
Longitudinal study of MRS metabolites in Rasmussen encephalitisR M Wellard, R S Briellmann, J C Wilson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 31, 2000
Phenotypic characterization of an alpha 4 neuronal nicotinic acetylcholine receptor subunit knock-out mouseS A Ross, J Y Wong, J J Clifford, et al.
AJNR. American Journal of Neuroradiology|October 13, 2022
Distinctive Brain Malformations in Zhu-Tokita-Takenouchi-Kim SyndromeB J Halliday, G Baynam, L Ewans, et al.
Nature Genetics|April 28, 2001
Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizuresR H Wallace, C Marini, S Petrou, et al.
Pageof 8