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Ingo Helbig

Showing results (101-110 of 270) with videos related to

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Neurology|September 23, 2025
Quantitative EEG Biomarkers in the Genetic Epilepsies and Associations With Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Ebiomedicine|August 27, 2022
Modulating effects of FGF12 variants on Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case seriesSimone Seiffert, Manuela Pendziwiat, Tatjana Bierhals, et al.
Medrxiv : the Preprint Server for Health Sciences|October 17, 2024
Quantitative EEG Spectral Features Differentiate Genetic Epilepsies and Predict Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 13, 2022
Current practice in diagnostic genetic testing of the epilepsiesIlona Krey, Konrad Platzer, Alina Esterhuizen, et al.
Epilepsia|June 18, 2022
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progressJuliet K Knowles, Ingo Helbig, Cameron S Metcalf, et al.
Epilepsy Research|June 23, 2018
PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanismEdward J Romasko, Elizabeth T DeChene, Jorune Balciuniene, et al.
Medrxiv : the Preprint Server for Health Sciences|October 3, 2025
Quantification of neuromotor control in <i>STXBP1</i> -Related Disorders with wearable sensorsJulie M Orlando, Bintou Bane, Torrey Chisari, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
Genome Medicine|April 28, 2022
SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencingDaniel Danis, Julius O B Jacobsen, Parithi Balachandran, et al.
European Journal of Human Genetics : EJHG|May 25, 2021
Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical dataDavid Lewis-Smith, Shiva Ganesan, Peter D Galer, et al.
Pageof 27

Showing results (101-110 of 270) with videos related to

Sort By:
Pageof 27
Neurology|September 23, 2025
Quantitative EEG Biomarkers in the Genetic Epilepsies and Associations With Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Ebiomedicine|August 27, 2022
Modulating effects of FGF12 variants on Na<sub>V</sub>1.2 and Na<sub>V</sub>1.6 being associated with developmental and epileptic encephalopathy and Autism spectrum disorder: A case seriesSimone Seiffert, Manuela Pendziwiat, Tatjana Bierhals, et al.
Medrxiv : the Preprint Server for Health Sciences|October 17, 2024
Quantitative EEG Spectral Features Differentiate Genetic Epilepsies and Predict Neurologic OutcomesPeter D Galer, Jillian L McKee, Sarah M Ruggiero, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 13, 2022
Current practice in diagnostic genetic testing of the epilepsiesIlona Krey, Konrad Platzer, Alina Esterhuizen, et al.
Epilepsia|June 18, 2022
Precision medicine for genetic epilepsy on the horizon: Recent advances, present challenges, and suggestions for continued progressJuliet K Knowles, Ingo Helbig, Cameron S Metcalf, et al.
Epilepsy Research|June 23, 2018
PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanismEdward J Romasko, Elizabeth T DeChene, Jorune Balciuniene, et al.
Medrxiv : the Preprint Server for Health Sciences|October 3, 2025
Quantification of neuromotor control in <i>STXBP1</i> -Related Disorders with wearable sensorsJulie M Orlando, Bintou Bane, Torrey Chisari, et al.
Epilepsy Research|January 12, 2013
The role of SLC2A1 in early onset and childhood absence epilepsiesHiltrud Muhle, Ingo Helbig, Tobias Guldberg Frøslev, et al.
Genome Medicine|April 28, 2022
SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencingDaniel Danis, Julius O B Jacobsen, Parithi Balachandran, et al.
European Journal of Human Genetics : EJHG|May 25, 2021
Phenotypic homogeneity in childhood epilepsies evolves in gene-specific patterns across 3251 patient-years of clinical dataDavid Lewis-Smith, Shiva Ganesan, Peter D Galer, et al.
Pageof 27