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Veronka Horber

Showing results (11-20 of 30) with videos related to

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Developmental Medicine and Child Neurology|June 22, 2016
MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendationsKate Himmelmann, Veronka Horber, Javier De La Cruz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 17, 2014
Clinical features of cerebral palsy in children with symptomatic congenital cytomegalovirus infectionIvana Dakovic, Maria da Graça Andrada, Teresa Folha, et al.
Developmental Medicine and Child Neurology|July 29, 2025
The distinction between the definition and description of cerebral palsyIngeborg Krägeloh-Mann, Javier de la Cruz, Malika Delobel-Ayoub, et al.
Frontiers in Neurology|May 16, 2020
Normative Observational Nerve Ultrasound Values in School-Age Children and Adolescents and Their Application to Hereditary NeuropathiesAnna-Sophie Grimm, Charlotte Schubert, Alexander Grimm, et al.
Frontiers in Pediatrics|November 30, 2023
High-sensitive cardiac troponin I (hs-cTnI) concentrations in newborns diagnosed with spinal muscular atrophyJessika Johannsen, Deike Weiss, Joenna Driemeyer, et al.
Neuropediatrics|March 3, 2020
The Origin of the Cerebral Palsies: Contribution of Population-Based Neuroimaging DataVeronka Horber, Elodie Sellier, Karen Horridge, et al.
Der Nervenarzt|May 13, 2020
[Recommendations for gene therapy of spinal muscular atrophy with onasemnogene abeparvovec-AVXS-101 : Consensus paper of the German representatives of the Society for Pediatric Neurology (GNP) and the German treatment centers with collaboration of the medical scientific advisory board of the German Society for Muscular Diseases (DGM)]Andreas Ziegler, Ekkehard Wilichowski, Ulrike Schara, et al.
European Journal of Human Genetics : EJHG|January 10, 2024
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorderFatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, et al.
Neurology|October 19, 2023
Prevalence, Clinical Features, Neuroimaging, and Genetic Findings in Children With Ataxic Cerebral Palsy in EuropeVeronka Horber, Guro L Andersen, Catherine Arnaud, et al.
Journal of Neuromuscular Diseases|November 21, 2019
Treatment with Nusinersen - Challenges Regarding the Indication for Children with SMA Type 1Astrid Pechmann, Matthias Baumann, Günther Bernert, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Developmental Medicine and Child Neurology|June 22, 2016
MRI classification system (MRICS) for children with cerebral palsy: development, reliability, and recommendationsKate Himmelmann, Veronka Horber, Javier De La Cruz, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 17, 2014
Clinical features of cerebral palsy in children with symptomatic congenital cytomegalovirus infectionIvana Dakovic, Maria da Graça Andrada, Teresa Folha, et al.
Developmental Medicine and Child Neurology|July 29, 2025
The distinction between the definition and description of cerebral palsyIngeborg Krägeloh-Mann, Javier de la Cruz, Malika Delobel-Ayoub, et al.
Frontiers in Neurology|May 16, 2020
Normative Observational Nerve Ultrasound Values in School-Age Children and Adolescents and Their Application to Hereditary NeuropathiesAnna-Sophie Grimm, Charlotte Schubert, Alexander Grimm, et al.
Frontiers in Pediatrics|November 30, 2023
High-sensitive cardiac troponin I (hs-cTnI) concentrations in newborns diagnosed with spinal muscular atrophyJessika Johannsen, Deike Weiss, Joenna Driemeyer, et al.
Neuropediatrics|March 3, 2020
The Origin of the Cerebral Palsies: Contribution of Population-Based Neuroimaging DataVeronka Horber, Elodie Sellier, Karen Horridge, et al.
Der Nervenarzt|May 13, 2020
[Recommendations for gene therapy of spinal muscular atrophy with onasemnogene abeparvovec-AVXS-101 : Consensus paper of the German representatives of the Society for Pediatric Neurology (GNP) and the German treatment centers with collaboration of the medical scientific advisory board of the German Society for Muscular Diseases (DGM)]Andreas Ziegler, Ekkehard Wilichowski, Ulrike Schara, et al.
European Journal of Human Genetics : EJHG|January 10, 2024
Confirmation and expansion of the phenotype of the TCEAL1-related neurodevelopmental disorderFatimah Albuainain, Yuwei Shi, Sarah Lor-Zade, et al.
Neurology|October 19, 2023
Prevalence, Clinical Features, Neuroimaging, and Genetic Findings in Children With Ataxic Cerebral Palsy in EuropeVeronka Horber, Guro L Andersen, Catherine Arnaud, et al.
Journal of Neuromuscular Diseases|November 21, 2019
Treatment with Nusinersen - Challenges Regarding the Indication for Children with SMA Type 1Astrid Pechmann, Matthias Baumann, Günther Bernert, et al.
Pageof 3