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I E Scheffer

Showing results (11-20 of 75) with videos related to

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Developmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M Brett
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Genetics of temporal lobe epilepsyL Vadlamudi, I E Scheffer, S F Berkovic
Annals of Neurology|January 23, 1999
Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndromeR Singh, I E Scheffer, K Crossland, et al.
Brain & Development|November 10, 2001
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)I E Scheffer, R Wallace, J C Mulley, et al.
Annals of Neurology|June 14, 2000
Locus for febrile seizuresI E Scheffer, R H Wallace, J C Mulley, et al.
Neuropediatrics|February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardationI E Scheffer, M Baraitser, J Wilson, et al.
Neurology|August 9, 2006
Electroclinical features of absence seizures in childhood absence epilepsyL G Sadleir, K Farrell, S Smith, et al.
Neurology|October 27, 1997
Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variationM Hayman, I E Scheffer, Y Chinvarun, et al.
Stem Cell Research|August 19, 2023
Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Na<sub>v</sub>1.2 protein encoded by the SCN2A geneD A Ovchinnikov, S Jong, C Cuddy, et al.
Epilepsia|May 10, 2000
Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsyO K Steinlein, J Stoodt, J Mulley, et al.
Pageof 8

Showing results (11-20 of 75) with videos related to

Sort By:
Pageof 8
Developmental Medicine and Child Neurology|October 1, 1991
Severe microcephaly associated with congenital varicella infectionI E Scheffer, M Baraitser, E M Brett
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Genetics of temporal lobe epilepsyL Vadlamudi, I E Scheffer, S F Berkovic
Annals of Neurology|January 23, 1999
Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndromeR Singh, I E Scheffer, K Crossland, et al.
Brain & Development|November 10, 2001
Clinical and molecular genetics of myoclonic-astatic epilepsy and severe myoclonic epilepsy in infancy (Dravet syndrome)I E Scheffer, R Wallace, J C Mulley, et al.
Annals of Neurology|June 14, 2000
Locus for febrile seizuresI E Scheffer, R H Wallace, J C Mulley, et al.
Neuropediatrics|February 1, 1992
Autosomal recessive microcephaly with severe psychomotor retardationI E Scheffer, M Baraitser, J Wilson, et al.
Neurology|August 9, 2006
Electroclinical features of absence seizures in childhood absence epilepsyL G Sadleir, K Farrell, S Smith, et al.
Neurology|October 27, 1997
Autosomal dominant nocturnal frontal lobe epilepsy: demonstration of focal frontal onset and intrafamilial variationM Hayman, I E Scheffer, Y Chinvarun, et al.
Stem Cell Research|August 19, 2023
Generation of an iPSC line (FINi001-A) from a girl with developmental and epileptic encephalopathy due to a heterozygous gain-of-function p.R1882Q variant in the voltage-gated sodium channel Na<sub>v</sub>1.2 protein encoded by the SCN2A geneD A Ovchinnikov, S Jong, C Cuddy, et al.
Epilepsia|May 10, 2000
Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsyO K Steinlein, J Stoodt, J Mulley, et al.
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