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Ingo Helbig

Showing results (51-60 of 292) with videos related to

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Annals of Neurology|December 27, 2016
ReplyKatherine L Helbig, Ulrike B S Hedrich, Ingrid E Scheffer, et al.
Molecular and Cellular Neurosciences|June 1, 2010
In vivo evidence for the involvement of the carboxy terminal domain in assembling connexin 36 at the electrical synapseIngo Helbig, Esther Sammler, Marina Eliava, et al.
Epilepsia|October 26, 2022
SCN1A gain-of-function mutation causing an early onset epileptic encephalopathyJérôme Clatot, Shridhar Parthasarathy, Stacey Cohen, et al.
Epilepsy Research|January 29, 2013
15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in BulgariaAndrey Kirov, Petia Dimova, Albena Todorova, et al.
Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.
Epilepsy Research|March 22, 2017
Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent patternMarkus von Deimling, Robert Häsler, Verena Steinbach, et al.
Epilepsy Research|November 20, 2013
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsiesJohanna A Jähn, Sarah von Spiczak, Hiltrud Muhle, et al.
Journal of Neurology|June 17, 2017
The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizuresKarl Martin Klein, Manuela Pendziwiat, Anda Eilam, et al.
Ebiomedicine|June 27, 2022
Predicting the functional effects of voltage-gated potassium channel missense variants with multi-task learningChristian Malte Boßelmann, Ulrike B S Hedrich, Peter Müller, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Pageof 30

Showing results (51-60 of 292) with videos related to

Sort By:
Pageof 30
Annals of Neurology|December 27, 2016
ReplyKatherine L Helbig, Ulrike B S Hedrich, Ingrid E Scheffer, et al.
Molecular and Cellular Neurosciences|June 1, 2010
In vivo evidence for the involvement of the carboxy terminal domain in assembling connexin 36 at the electrical synapseIngo Helbig, Esther Sammler, Marina Eliava, et al.
Epilepsia|October 26, 2022
SCN1A gain-of-function mutation causing an early onset epileptic encephalopathyJérôme Clatot, Shridhar Parthasarathy, Stacey Cohen, et al.
Epilepsy Research|January 29, 2013
15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in BulgariaAndrey Kirov, Petia Dimova, Albena Todorova, et al.
Epilepsia|November 5, 2011
Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndromeHiltrud Muhle, Heather C Mefford, Tanja Obermeier, et al.
Epilepsy Research|March 22, 2017
Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent patternMarkus von Deimling, Robert Häsler, Verena Steinbach, et al.
Epilepsy Research|November 20, 2013
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsiesJohanna A Jähn, Sarah von Spiczak, Hiltrud Muhle, et al.
Journal of Neurology|June 17, 2017
The phenotypic spectrum of ARHGEF9 includes intellectual disability, focal epilepsy and febrile seizuresKarl Martin Klein, Manuela Pendziwiat, Anda Eilam, et al.
Ebiomedicine|June 27, 2022
Predicting the functional effects of voltage-gated potassium channel missense variants with multi-task learningChristian Malte Boßelmann, Ulrike B S Hedrich, Peter Müller, et al.
Neurogenetics|March 29, 2018
Genetic test utilization and diagnostic yield in adult patients with neurological disordersTanya M Bardakjian, Ingo Helbig, Colin Quinn, et al.
Pageof 30