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Showing results (81-90 of 94) with videos related to

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Parkinsonism & Related Disorders|July 25, 2022
Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomesIvana Dzinovic, Sylvia Boesch, Matej Škorvánek, et al.
Acta Neuropathologica Communications|December 7, 2019
The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migrationMelanie Schoof, Michael Launspach, Dörthe Holdhof, et al.
Child Maltreatment|July 4, 2025
Lost Narratives: Identifying Predictors of Attrition and Differences in Recruitment Effort in a Longitudinal Study on Child MaltreatmentJan Keil, Josephine Breuer, Romy Küchler, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
European Journal of Public Health|February 15, 2022
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Neuropediatrics|September 5, 2014
Use of intrathecal baclofen in children and adolescents: interdisciplinary consensus table 2013Steffen Berweck, Sonnhild Lütjen, Wolfgang Voss, et al.
Annals of Neurology|November 5, 2022
Recessive NUP54 Variants Underlie Early-Onset Dystonia with Striatal LesionsPhilip Harrer, Audrey Schalk, Masaru Shimura, et al.
Parkinsonism & Related Disorders|February 21, 2021
Clinically relevant copy-number variants in exome sequencing data of patients with dystoniaMichael Zech, Sylvia Boesch, Matej Škorvánek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsySakshi Singh, Aditi Gupta, Michael Zech, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2021
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation StudyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Pageof 10

Showing results (81-90 of 94) with videos related to

Sort By:
Pageof 10
Parkinsonism & Related Disorders|July 25, 2022
Genetic overlap between dystonia and other neurologic disorders: A study of 1,100 exomesIvana Dzinovic, Sylvia Boesch, Matej Škorvánek, et al.
Acta Neuropathologica Communications|December 7, 2019
The transcriptional coactivator and histone acetyltransferase CBP regulates neural precursor cell development and migrationMelanie Schoof, Michael Launspach, Dörthe Holdhof, et al.
Child Maltreatment|July 4, 2025
Lost Narratives: Identifying Predictors of Attrition and Differences in Recruitment Effort in a Longitudinal Study on Child MaltreatmentJan Keil, Josephine Breuer, Romy Küchler, et al.
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
European Journal of Public Health|February 15, 2022
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI studyVeronika Sanin, Raphael Schmieder, Sara Ates, et al.
Neuropediatrics|September 5, 2014
Use of intrathecal baclofen in children and adolescents: interdisciplinary consensus table 2013Steffen Berweck, Sonnhild Lütjen, Wolfgang Voss, et al.
Annals of Neurology|November 5, 2022
Recessive NUP54 Variants Underlie Early-Onset Dystonia with Striatal LesionsPhilip Harrer, Audrey Schalk, Masaru Shimura, et al.
Parkinsonism & Related Disorders|February 21, 2021
Clinically relevant copy-number variants in exome sequencing data of patients with dystoniaMichael Zech, Sylvia Boesch, Matej Škorvánek, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 6, 2020
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsySakshi Singh, Aditi Gupta, Michael Zech, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 5, 2021
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation StudyMichael Zech, Robert Jech, Sylvia Boesch, et al.
Pageof 10