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Showing results (171-180 of 270) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
Science Advances|April 15, 2026
Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretationRobert Wang, Feng Wang, Nicole DeBruyne, et al.
Ebiomedicine|January 6, 2026
Paediatric cerebrospinal fluid immune profiling distinguishes paediatric-onset multiple sclerosis from other paediatric-onset acute neurological disordersDiego A Espinoza, Tobias Zrzavy, Gautier Breville, et al.
Human Molecular Genetics|February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsyMichel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
Brain Communications|December 15, 2021
Variants in <i>ATP6V0A1</i> cause progressive myoclonus epilepsy and developmental and epileptic encephalopathyLaura C Bott, Mitra Forouhan, Maria Lieto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Genetic variants in <i>DDX53</i> contribute to Autism Spectrum Disorder associated with the Xp22.11 locusMarcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
Epilepsia|December 28, 2020
Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care systemZachary M Grinspan, Anup D Patel, Renée A Shellhaas, et al.
Brain : a Journal of Neurology|September 20, 2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasiaKatia Hardies, Carolien G F de Kovel, Sarah Weckhuysen, 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.
Biorxiv : the Preprint Server for Biology|March 3, 2025
Comparative molecular landscapes of immature neurons in the mammalian dentate gyrus across species reveal special features in humansYi Zhou, Yijing Su, Qian Yang, et al.
Pageof 27

Showing results (171-180 of 270) with videos related to

Sort By:
Pageof 27
Epileptic Disorders : International Epilepsy Journal with Videotape|July 21, 2016
Idiopathic focal epilepsies: the "lost tribe"Deb K Pal, Colin Ferrie, Laura Addis, et al.
Science Advances|April 15, 2026
Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretationRobert Wang, Feng Wang, Nicole DeBruyne, et al.
Ebiomedicine|January 6, 2026
Paediatric cerebrospinal fluid immune profiling distinguishes paediatric-onset multiple sclerosis from other paediatric-onset acute neurological disordersDiego A Espinoza, Tobias Zrzavy, Gautier Breville, et al.
Human Molecular Genetics|February 19, 2015
Galanin pathogenic mutations in temporal lobe epilepsyMichel Guipponi, Amina Chentouf, Kristin E B Webling, et al.
Brain Communications|December 15, 2021
Variants in <i>ATP6V0A1</i> cause progressive myoclonus epilepsy and developmental and epileptic encephalopathyLaura C Bott, Mitra Forouhan, Maria Lieto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 18, 2024
Genetic variants in <i>DDX53</i> contribute to Autism Spectrum Disorder associated with the Xp22.11 locusMarcello Scala, Clarrisa A Bradley, Jennifer L Howe, et al.
Epilepsia|December 28, 2020
Design and implementation of electronic health record common data elements for pediatric epilepsy: Foundations for a learning health care systemZachary M Grinspan, Anup D Patel, Renée A Shellhaas, et al.
Brain : a Journal of Neurology|September 20, 2015
Recessive mutations in SLC13A5 result in a loss of citrate transport and cause neonatal epilepsy, developmental delay and teeth hypoplasiaKatia Hardies, Carolien G F de Kovel, Sarah Weckhuysen, 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.
Biorxiv : the Preprint Server for Biology|March 3, 2025
Comparative molecular landscapes of immature neurons in the mammalian dentate gyrus across species reveal special features in humansYi Zhou, Yijing Su, Qian Yang, et al.
Pageof 27