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Hannah Stamberger

Showing results (1-10 of 26) with videos related to

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Expert Opinion on Therapeutic Targets|October 4, 2017
STXBP1 as a therapeutic target for epileptic encephalopathyHannah Stamberger, Sarah Weckhuysen, Peter De Jonghe
JCI Insight|February 13, 2025
Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndromeSheng Tang, Hannah Stamberger, Jeffrey D Calhoun, et al.
Neural Plasticity|January 15, 2015
Auditory cortex tACS and tRNS for tinnitus: single versus multiple sessionsLaura Claes, Hannah Stamberger, Paul Van de Heyning, et al.
Brain : a Journal of Neurology|November 17, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathiesSathiya N Manivannan, Jolien Roovers, Noor Smal, et al.
Human Mutation|April 14, 2025
Heterozygous Missense Variants in the ATPase Phospholipid Transporting 9A Gene, <i>ATP9A</i>, Alter Dendritic Spine Maturation and Cause Dominantly Inherited Nonsyndromic Intellectual DisabilityAmélie Cordovado, Yvan Hérenger, Coline Cormier, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 5, 2019
Treatment Responsiveness in KCNT1-Related EpilepsyMark P Fitzgerald, Martina Fiannacca, Douglas M Smith, et al.
Ebiomedicine|July 30, 2025
SUDEP risk is influenced by longevity genomics: a polygenic risk score studyHelena Martins, James D Mills, Susanna Pagni, et al.
American Journal of Human Genetics|December 12, 2018
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic EpilepsiesGemma L Carvill, Krysta L Engel, Aishwarya Ramamurthy, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patientsCarolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Nature Genetics|June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsyHenrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Expert Opinion on Therapeutic Targets|October 4, 2017
STXBP1 as a therapeutic target for epileptic encephalopathyHannah Stamberger, Sarah Weckhuysen, Peter De Jonghe
JCI Insight|February 13, 2025
Antisense oligonucleotides modulate aberrant inclusion of poison exons in SCN1A-related Dravet syndromeSheng Tang, Hannah Stamberger, Jeffrey D Calhoun, et al.
Neural Plasticity|January 15, 2015
Auditory cortex tACS and tRNS for tinnitus: single versus multiple sessionsLaura Claes, Hannah Stamberger, Paul Van de Heyning, et al.
Brain : a Journal of Neurology|November 17, 2021
De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathiesSathiya N Manivannan, Jolien Roovers, Noor Smal, et al.
Human Mutation|April 14, 2025
Heterozygous Missense Variants in the ATPase Phospholipid Transporting 9A Gene, <i>ATP9A</i>, Alter Dendritic Spine Maturation and Cause Dominantly Inherited Nonsyndromic Intellectual DisabilityAmélie Cordovado, Yvan Hérenger, Coline Cormier, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 5, 2019
Treatment Responsiveness in KCNT1-Related EpilepsyMark P Fitzgerald, Martina Fiannacca, Douglas M Smith, et al.
Ebiomedicine|July 30, 2025
SUDEP risk is influenced by longevity genomics: a polygenic risk score studyHelena Martins, James D Mills, Susanna Pagni, et al.
American Journal of Human Genetics|December 12, 2018
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic EpilepsiesGemma L Carvill, Krysta L Engel, Aishwarya Ramamurthy, et al.
Molecular Genetics & Genomic Medicine|September 22, 2016
Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patientsCarolien G F de Kovel, Eva H Brilstra, Marjan J A van Kempen, et al.
Nature Genetics|June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsyHenrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.
Pageof 3