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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 study
Janina 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-23
Peter 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 approaches
Felix 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 Tests
Jeroen 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 investigation
Florien 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 Germany
Laurent 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' Perspectives
Laurent 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 Phenotypes
Carolien 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 Adulthood
Hannah Stamberger, David Crosiers, Ganna Balagura, et al.
Nature Genetics
|
April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Leanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
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Search research articles
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Showing results (361-370 of 379) with videos related to
Sort By:
Page
of 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 study
Janina 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-23
Peter 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 approaches
Felix 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 Tests
Jeroen 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 investigation
Florien 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 Germany
Laurent 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' Perspectives
Laurent 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 Phenotypes
Carolien 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 Adulthood
Hannah Stamberger, David Crosiers, Ganna Balagura, et al.
Nature Genetics
|
April 2, 2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Leanne M Dibbens, Boukje de Vries, Simona Donatello, et al.
Page
of 38