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Thomas Bast

Showing results (91-100 of 106) with videos related to

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Neuropediatrics|August 30, 2024
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly PatientsChristiane R Proepper, Sofia M Schuetz, Lisa-Maria Schwarz, et al.
Epilepsia Open|January 24, 2023
Real-world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter studyFabienne Kühne, Lena-Luise Becker, Thomas Bast, et al.
Orphanet Journal of Rare Diseases|May 23, 2026
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephalyChristiane R Proepper, Lisa-Maria Schwarz, Sofia M Schuetz, et al.
Orphanet Journal of Rare Diseases|June 22, 2021
Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort studyJanina Grau, Johann Philipp Zöllner, Susanne Schubert-Bast, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathwayGregory M Enns, Vandana Shashi, Matthew Bainbridge, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 21, 2021
Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from GermanyLaurent M Willems, Susanne Schubert-Bast, Janina Grau, et al.
CNS Drugs|July 18, 2021
Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients' PerspectivesLaurent M Willems, Felix Rosenow, Susanne Schubert-Bast, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.
Biomedicines|October 31, 2020
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in ChildhoodJan Henje Döring, Afshin Saffari, Thomas Bast, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- miceMilka Pringsheim, Diana Mitter, Simone Schröder, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Neuropediatrics|August 30, 2024
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly PatientsChristiane R Proepper, Sofia M Schuetz, Lisa-Maria Schwarz, et al.
Epilepsia Open|January 24, 2023
Real-world data on cannabidiol treatment of various epilepsy subtypes: A retrospective, multicenter studyFabienne Kühne, Lena-Luise Becker, Thomas Bast, et al.
Orphanet Journal of Rare Diseases|May 23, 2026
Gene-specific long-term course, neurodevelopmental outcome and quality of life in patients with LIS1/PAFAH1B1-, DCX-, DYNC1H1-, TUBA1A- and TUBG1-related lissencephalyChristiane R Proepper, Lisa-Maria Schwarz, Sofia M Schuetz, et al.
Orphanet Journal of Rare Diseases|June 22, 2021
Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort studyJanina Grau, Johann Philipp Zöllner, Susanne Schubert-Bast, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 22, 2014
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum-associated degradation pathwayGregory M Enns, Vandana Shashi, Matthew Bainbridge, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 21, 2021
Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from GermanyLaurent M Willems, Susanne Schubert-Bast, Janina Grau, et al.
CNS Drugs|July 18, 2021
Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients' PerspectivesLaurent M Willems, Felix Rosenow, Susanne Schubert-Bast, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.
Biomedicines|October 31, 2020
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in ChildhoodJan Henje Döring, Afshin Saffari, Thomas Bast, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- miceMilka Pringsheim, Diana Mitter, Simone Schröder, et al.
Pageof 11