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Anna C Jansen

Showing results (51-60 of 97) with videos related to

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Annals of Neurology|November 12, 2020
Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP TrialKatarzyna Kotulska, David J Kwiatkowski, Paolo Curatolo, et al.
Brain : a Journal of Neurology|July 26, 2024
Prenatal assessment of brain malformations on neuroimaging: an expert panel reviewIvana Pogledic, Kshitij Mankad, Mariasavina Severino, et al.
Epilepsia|March 29, 2021
Early epileptiform EEG activity in infants with tuberous sclerosis complex predicts epilepsy and neurodevelopmental outcomesJessie De Ridder, Birgit Verhelle, Jan Vervisch, et al.
Journal of Medical Genetics|June 24, 2020
Defining the phenotypical spectrum associated with variants in <i>TUBB2A</i>Stefanie Brock, Tim Vanderhasselt, Sietske Vermaning, et al.
Journal of Neuropathology and Experimental Neurology|September 21, 2020
Myelin Pathology Beyond White Matter in Tuberous Sclerosis Complex (TSC) Cortical TubersAngelika Mühlebner, Jackelien van Scheppingen, Andrew de Neef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformationIne Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Frontiers in Psychiatry|March 17, 2022
Empowering Families Through Technology: A Mobile-Health Project to Reduce the TAND Identification and Treatment Gap (TANDem)Tosca-Marie Heunis, Stacey Bissell, Anna W Byars, et al.
Frontiers in Neurology|November 12, 2020
Prediction of Neurodevelopment in Infants With Tuberous Sclerosis Complex Using Early EEG CharacteristicsJessie De Ridder, Mario Lavanga, Birgit Verhelle, et al.
Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
Annals of Neurology|November 12, 2020
Prevention of Epilepsy in Infants with Tuberous Sclerosis Complex in the EPISTOP TrialKatarzyna Kotulska, David J Kwiatkowski, Paolo Curatolo, et al.
Brain : a Journal of Neurology|July 26, 2024
Prenatal assessment of brain malformations on neuroimaging: an expert panel reviewIvana Pogledic, Kshitij Mankad, Mariasavina Severino, et al.
Epilepsia|March 29, 2021
Early epileptiform EEG activity in infants with tuberous sclerosis complex predicts epilepsy and neurodevelopmental outcomesJessie De Ridder, Birgit Verhelle, Jan Vervisch, et al.
Journal of Medical Genetics|June 24, 2020
Defining the phenotypical spectrum associated with variants in <i>TUBB2A</i>Stefanie Brock, Tim Vanderhasselt, Sietske Vermaning, et al.
Journal of Neuropathology and Experimental Neurology|September 21, 2020
Myelin Pathology Beyond White Matter in Tuberous Sclerosis Complex (TSC) Cortical TubersAngelika Mühlebner, Jackelien van Scheppingen, Andrew de Neef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 30, 2025
Bilateral frontal periventricular nodular heterotopia: a distinctive cortical malformationIne Hoogwijs, Simone A Mandelstam, George McGillivray, et al.
American Journal of Human Genetics|January 19, 2022
Impaired catabolism of free oligosaccharides due to MAN2C1 variants causes a neurodevelopmental disorderNuno Maia, Sven Potelle, Hamide Yildirim, et al.
Frontiers in Psychiatry|March 17, 2022
Empowering Families Through Technology: A Mobile-Health Project to Reduce the TAND Identification and Treatment Gap (TANDem)Tosca-Marie Heunis, Stacey Bissell, Anna W Byars, et al.
Frontiers in Neurology|November 12, 2020
Prediction of Neurodevelopment in Infants With Tuberous Sclerosis Complex Using Early EEG CharacteristicsJessie De Ridder, Mario Lavanga, Birgit Verhelle, et al.
Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.
Pageof 10