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Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla 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 Spectrum
Kristy L Kolc, Rikke S Møller, Lynette G Sadleir, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
March 15, 2021
The aetiologies of epilepsy
Simona 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 phenotype
Cherie 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 genes
Karen L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Molecular Psychiatry
|
February 17, 2024
Genetic architecture of childhood speech disorder: a review
Angela 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 epilepsy
Smriti 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 impairment
Alison 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 release
Marco Fedi, Leon A Bach, Samuel F Berkovic, et al.
Page
of 59
Search research articles
Search
Showing results (121-130 of 586) with videos related to
Sort By:
Page
of 59
Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla 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 Spectrum
Kristy L Kolc, Rikke S Møller, Lynette G Sadleir, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
March 15, 2021
The aetiologies of epilepsy
Simona 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 phenotype
Cherie 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 genes
Karen L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Molecular Psychiatry
|
February 17, 2024
Genetic architecture of childhood speech disorder: a review
Angela 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 epilepsy
Smriti 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 impairment
Alison 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 release
Marco Fedi, Leon A Bach, Samuel F Berkovic, et al.
Page
of 59