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E Scheffer

Showing results (211-220 of 740) with videos related to

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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.
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.
Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Human Mutation|May 10, 2005
SCN1A mutations and epilepsyJohn C Mulley, Ingrid E Scheffer, Steven Petrou, et al.
Virchows Archiv. B, Cell Pathology|September 17, 1976
Further evidence for the T-cell nature of the atypical mononuclear cells in mycosis fungoidesA W van Leeuwen, C J Meijer, W A van Vloten, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Epilepsia|July 12, 2008
Factors influencing clinical features of absence seizuresLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Pageof 74

Showing results (211-220 of 740) with videos related to

Sort By:
Pageof 74
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.
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.
Epilepsia|February 22, 2023
Genes4Epilepsy: An epilepsy gene resourceKaren L Oliver, Ingrid E Scheffer, Mark F Bennett, et al.
Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (IALP)|July 23, 2019
Looking to the Future: Speech, Language, and Academic Outcomes in an Adolescent with Childhood Apraxia of SpeechSamantha J Turner, Adam P Vogel, Bronwyn Parry-Fielder, et al.
Human Mutation|May 10, 2005
SCN1A mutations and epilepsyJohn C Mulley, Ingrid E Scheffer, Steven Petrou, et al.
Virchows Archiv. B, Cell Pathology|September 17, 1976
Further evidence for the T-cell nature of the atypical mononuclear cells in mycosis fungoidesA W van Leeuwen, C J Meijer, W A van Vloten, et al.
Annals of Neurology|August 12, 2000
A de novo mutation in sporadic nocturnal frontal lobe epilepsyH A Phillips, C Marini, I E Scheffer, et al.
Epilepsia|July 12, 2008
Factors influencing clinical features of absence seizuresLynette G Sadleir, Ingrid E Scheffer, Sherry Smith, et al.
Pageof 74