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Ingrid E Scheffer

Showing results (121-130 of 586) with videos related to

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Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Advances in Experimental Medicine and Biology|August 28, 2020
PCDH19 Pathogenic Variants in Males: Expanding the Phenotypic SpectrumKristy L Kolc, Rikke S Møller, Lynette G Sadleir, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 15, 2021
The aetiologies of epilepsySimona Balestrini, Alexis Arzimanoglou, Ingmar Blümcke, et al.
Autism Research : Official Journal of the International Society for Autism Research|October 1, 2019
Cognitive processes predicting advanced theory of mind in the broader autism phenotypeCherie C Green, Natasha J Brown, Valerie M Z Yap, et al.
Plos One|July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genesKaren L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Molecular Psychiatry|February 17, 2024
Genetic architecture of childhood speech disorder: a reviewAngela T Morgan, David J Amor, Miya D St John, et al.
Brain Pathology (Zurich, Switzerland)|August 28, 2020
Medullary tyrosine hydroxylase catecholaminergic neuronal populations in sudden unexpected death in epilepsySmriti Patodia, Ian Tan, Matthew Ellis, et al.
Epilepsia|April 29, 2005
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?Nigel C K Tan, Sarah E Heron, Ingrid E Scheffer, et al.
European Journal of Medical Genetics|September 24, 2009
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairmentAlison Yeung, Damien Bruno, Ingrid E Scheffer, et al.
The Journal of Clinical Endocrinology and Metabolism|November 29, 2007
Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone releaseMarco Fedi, Leon A Bach, Samuel F Berkovic, et al.
Pageof 59

Showing results (121-130 of 586) with videos related to

Sort By:
Pageof 59
Epilepsia|April 6, 2011
The genetics of Dravet syndromeCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Advances in Experimental Medicine and Biology|August 28, 2020
PCDH19 Pathogenic Variants in Males: Expanding the Phenotypic SpectrumKristy L Kolc, Rikke S Møller, Lynette G Sadleir, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 15, 2021
The aetiologies of epilepsySimona Balestrini, Alexis Arzimanoglou, Ingmar Blümcke, et al.
Autism Research : Official Journal of the International Society for Autism Research|October 1, 2019
Cognitive processes predicting advanced theory of mind in the broader autism phenotypeCherie C Green, Natasha J Brown, Valerie M Z Yap, et al.
Plos One|July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genesKaren L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Molecular Psychiatry|February 17, 2024
Genetic architecture of childhood speech disorder: a reviewAngela T Morgan, David J Amor, Miya D St John, et al.
Brain Pathology (Zurich, Switzerland)|August 28, 2020
Medullary tyrosine hydroxylase catecholaminergic neuronal populations in sudden unexpected death in epilepsySmriti Patodia, Ian Tan, Matthew Ellis, et al.
Epilepsia|April 29, 2005
Is variation in the GABA(B) receptor 1 gene associated with temporal lobe epilepsy?Nigel C K Tan, Sarah E Heron, Ingrid E Scheffer, et al.
European Journal of Medical Genetics|September 24, 2009
4.45 Mb microduplication in chromosome band 14q12 including FOXG1 in a girl with refractory epilepsy and intellectual impairmentAlison Yeung, Damien Bruno, Ingrid E Scheffer, et al.
The Journal of Clinical Endocrinology and Metabolism|November 29, 2007
Association of a nicotinic receptor mutation with reduced height and blunted physostigmine-stimulated growth hormone releaseMarco Fedi, Leon A Bach, Samuel F Berkovic, et al.
Pageof 59