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I E Scheffer

Showing results (41-50 of 75) with videos related to

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Neurology|December 28, 2006
Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adultsF E Jansen, L G Sadleir, L A Harkin, et al.
Annals of Neurology|December 16, 1998
Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2I E Scheffer, H A Phillips, C E O'Brien, et al.
Neuroscience Letters|May 12, 2009
The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsiesL M Dibbens, L A Harkin, M Richards, et al.
Neurology|September 29, 2004
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsyN C K Tan, S E Heron, I E Scheffer, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Neurology|October 26, 1999
Motor cortex localization using functional MRI and transcranial magnetic stimulationR A Macdonell, G D Jackson, J M Curatolo, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology|September 27, 2006
A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1AJ C Mulley, P Nelson, S Guerrero, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Neurology|December 28, 2006
Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adultsF E Jansen, L G Sadleir, L A Harkin, et al.
Annals of Neurology|December 16, 1998
Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2I E Scheffer, H A Phillips, C E O'Brien, et al.
Neuroscience Letters|May 12, 2009
The role of neuronal GABA(A) receptor subunit mutations in idiopathic generalized epilepsiesL M Dibbens, L A Harkin, M Richards, et al.
Neurology|September 29, 2004
Failure to confirm association of a polymorphism in ABCB1 with multidrug-resistant epilepsyN C K Tan, S E Heron, I E Scheffer, et al.
Epilepsy Research|November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locusI Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology|February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Journal of Medical Genetics|August 7, 2007
Deletions or duplications in KCNQ2 can cause benign familial neonatal seizuresS E Heron, K Cox, B E Grinton, et al.
Neurology|October 26, 1999
Motor cortex localization using functional MRI and transcranial magnetic stimulationR A Macdonell, G D Jackson, J M Curatolo, et al.
Lancet (London, England)|February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorderI E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology|September 27, 2006
A new molecular mechanism for severe myoclonic epilepsy of infancy: exonic deletions in SCN1AJ C Mulley, P Nelson, S Guerrero, et al.
Pageof 8