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I E Scheffer

Showing results (31-40 of 75) with videos related to

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Neurology|August 24, 2005
Familial clustering of seizure types within the idiopathic generalized epilepsiesM R Winawer, C Marini, B E Grinton, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Neurology|August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD responseP W Carney, R A J Masterton, A S Harvey, et al.
Neurology|April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequenceK M Klein, S C Yendle, A S Harvey, et al.
Journal of Paediatrics and Child Health|November 25, 2003
The health-related quality of life of childhood epilepsy syndromesM Sabaz, D R Cairns, A F Bleasel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Journal of Medical Genetics|February 27, 2004
Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interactionM C Richards, S E Heron, H E Spendlove, et al.
Neurology|May 16, 2002
Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1BR H Wallace, I E Scheffer, G Parasivam, et al.
Neurology|August 8, 2008
Reduced striatal D1 receptor binding in autosomal dominant nocturnal frontal lobe epilepsyM Fedi, S F Berkovic, I E Scheffer, et al.
Nature Genetics|October 1, 1995
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, J C Mulley, P Propping, et al.
Pageof 8

Showing results (31-40 of 75) with videos related to

Sort By:
Pageof 8
Neurology|August 24, 2005
Familial clustering of seizure types within the idiopathic generalized epilepsiesM R Winawer, C Marini, B E Grinton, et al.
Nature Genetics|May 1, 1995
Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q 13.2H A Phillips, I E Scheffer, S F Berkovic, et al.
Neurology|August 13, 2010
The core network in absence epilepsy. Differences in cortical and thalamic BOLD responseP W Carney, R A J Masterton, A S Harvey, et al.
Neurology|April 20, 2011
A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequenceK M Klein, S C Yendle, A S Harvey, et al.
Journal of Paediatrics and Child Health|November 25, 2003
The health-related quality of life of childhood epilepsy syndromesM Sabaz, D R Cairns, A F Bleasel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 18, 2005
Superior verbal ability and nonverbal learning disability in a child with a novel 17p12p13.1 deletionD L Steele, A K Chisholm, J D R McGhie, et al.
Journal of Medical Genetics|February 27, 2004
Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interactionM C Richards, S E Heron, H E Spendlove, et al.
Neurology|May 16, 2002
Generalized epilepsy with febrile seizures plus: mutation of the sodium channel subunit SCN1BR H Wallace, I E Scheffer, G Parasivam, et al.
Neurology|August 8, 2008
Reduced striatal D1 receptor binding in autosomal dominant nocturnal frontal lobe epilepsyM Fedi, S F Berkovic, I E Scheffer, et al.
Nature Genetics|October 1, 1995
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, J C Mulley, P Propping, et al.
Pageof 8