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Martin Klein

Showing results (361-370 of 379) with videos related to

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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.
Cancers|July 24, 2021
Development of Randomized Trials in Adults with Medulloblastoma-The Example of EORTC 1634-BTG/NOA-23Peter Hau, Didier Frappaz, Elizabeth Hovey, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2018
Detecting Mild Cognitive Deficits in Parkinson's Disease: Comparison of Neuropsychological TestsJeroen Hoogland, Lennard L van Wanrooij, Judith A Boel, et al.
Neuro-Oncology|July 22, 2025
Health-related quality of life and cognitive functioning in survivors of oligodendroglioma: an international cross-sectional investigationFlorien W Boele, Sé M Frances, Amélie Darlix, 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.
JAMA Neurology|August 15, 2017
Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and PhenotypesCarolien G F de Kovel, Steffen Syrbe, Eva H Brilstra, et al.
Neurology|July 19, 2022
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into AdulthoodHannah Stamberger, David Crosiers, Ganna Balagura, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Pageof 38

Showing results (361-370 of 379) with videos related to

Sort By:
Pageof 38
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.
Cancers|July 24, 2021
Development of Randomized Trials in Adults with Medulloblastoma-The Example of EORTC 1634-BTG/NOA-23Peter Hau, Didier Frappaz, Elizabeth Hovey, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2018
Detecting Mild Cognitive Deficits in Parkinson's Disease: Comparison of Neuropsychological TestsJeroen Hoogland, Lennard L van Wanrooij, Judith A Boel, et al.
Neuro-Oncology|July 22, 2025
Health-related quality of life and cognitive functioning in survivors of oligodendroglioma: an international cross-sectional investigationFlorien W Boele, Sé M Frances, Amélie Darlix, 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.
JAMA Neurology|August 15, 2017
Neurodevelopmental Disorders Caused by De Novo Variants in KCNB1 Genotypes and PhenotypesCarolien G F de Kovel, Steffen Syrbe, Eva H Brilstra, et al.
Neurology|July 19, 2022
Natural History Study of STXBP1-Developmental and Epileptic Encephalopathy Into AdulthoodHannah Stamberger, David Crosiers, Ganna Balagura, et al.
Nature Genetics|April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable fociLeanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Pageof 38