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Kate Riney

Showing results (41-50 of 54) with videos related to

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Annals of Clinical and Translational Neurology|July 25, 2020
Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?Romina Moavero, Katarzyna Kotulska, Lieven Lagae, et al.
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.
Epilepsia|February 5, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsyMarsha Tan, Beatrice Southby Goad, Meagan Allen, et al.
Neurology|February 1, 2022
Association of Early MRI Characteristics With Subsequent Epilepsy and Neurodevelopmental Outcomes in Children With Tuberous Sclerosis ComplexHanna M Hulshof, Hugo J Kuijf, Katarzyna Kotulska, 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.
Brain Communications|March 6, 2024
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformationsDaniz Kooshavar, David J Amor, Kirsten Boggs, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 29, 2020
TSC2 pathogenic variants are predictive of severe clinical manifestations in TSC infants: results of the EPISTOP studyBarbara Ogórek, Lana Hamieh, Hanna M Hulshof, et al.
Brain : a Journal of Neurology|March 20, 2014
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcomePhilippa B Mills, Stephane S M Camuzeaux, Emma J Footitt, et al.
Biomedicines|August 26, 2022
miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis ComplexMirte Scheper, Alessia Romagnolo, Zein Mersini Besharat, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Annals of Clinical and Translational Neurology|July 25, 2020
Is autism driven by epilepsy in infants with Tuberous Sclerosis Complex?Romina Moavero, Katarzyna Kotulska, Lieven Lagae, et al.
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.
Epilepsia|February 5, 2026
Mechanisms of SCN2A loss of function do not predict presence or phenotype of epilepsyMarsha Tan, Beatrice Southby Goad, Meagan Allen, et al.
Neurology|February 1, 2022
Association of Early MRI Characteristics With Subsequent Epilepsy and Neurodevelopmental Outcomes in Children With Tuberous Sclerosis ComplexHanna M Hulshof, Hugo J Kuijf, Katarzyna Kotulska, 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.
Brain Communications|March 6, 2024
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformationsDaniz Kooshavar, David J Amor, Kirsten Boggs, 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.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 29, 2020
TSC2 pathogenic variants are predictive of severe clinical manifestations in TSC infants: results of the EPISTOP studyBarbara Ogórek, Lana Hamieh, Hanna M Hulshof, et al.
Brain : a Journal of Neurology|March 20, 2014
Epilepsy due to PNPO mutations: genotype, environment and treatment affect presentation and outcomePhilippa B Mills, Stephane S M Camuzeaux, Emma J Footitt, et al.
Biomedicines|August 26, 2022
miRNAs and isomiRs: Serum-Based Biomarkers for the Development of Intellectual Disability and Autism Spectrum Disorder in Tuberous Sclerosis ComplexMirte Scheper, Alessia Romagnolo, Zein Mersini Besharat, et al.
Pageof 6