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Martin Staudt

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

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Plos One|July 19, 2018
Effects of visual search training in children with hemianopiaIliya V Ivanov, Stephan Kuester, Manfred MacKeben, et al.
Frontiers in Neurology|May 31, 2021
Deep Brain Stimulation in KMT2B-Related Dystonia: Case Report and Review of the Literature With Special Emphasis on Dysarthria and SpeechMaria Abel, Robert Pfister, Iman Hussein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 5, 2014
Microstructure of transcallosal motor fibers reflects type of cortical (re-)organization in congenital hemiparesisHendrik Juenger, Inga K Koerte, Marc Muehlmann, et al.
Developmental Medicine and Child Neurology|August 14, 2013
Two types of exercise-induced neuroplasticity in congenital hemiparesis: a transcranial magnetic stimulation, functional MRI, and magnetoencephalography studyHendrik Juenger, Nicola Kuhnke, Christoph Braun, et al.
Epilepsy Research|September 15, 2012
Etiology-specific differences in motor function after hemispherectomyNicolien M van der Kolk, Kim Boshuisen, Ron van Empelen, et al.
Epilepsia|November 6, 2021
Multilobar unilateral hypoplasia with emphasis on the posterior quadrant and severe epilepsy in children with FCD ILAE Type 1AHans Holthausen, Roland Coras, Yingying Tang, et al.
Neuropediatrics|March 3, 2015
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiencesAnna Biró, Ulrich Stephani, Tiziana Tarallo, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutationsLadislav Kuchar, Jana Ledvinová, Martin Hrebícek, et al.
Nature Medicine|April 22, 2025
Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathyMatias Wagner, Géza Berecki, Walid Fazeli, 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 9

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

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
Plos One|July 19, 2018
Effects of visual search training in children with hemianopiaIliya V Ivanov, Stephan Kuester, Manfred MacKeben, et al.
Frontiers in Neurology|May 31, 2021
Deep Brain Stimulation in KMT2B-Related Dystonia: Case Report and Review of the Literature With Special Emphasis on Dysarthria and SpeechMaria Abel, Robert Pfister, Iman Hussein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 5, 2014
Microstructure of transcallosal motor fibers reflects type of cortical (re-)organization in congenital hemiparesisHendrik Juenger, Inga K Koerte, Marc Muehlmann, et al.
Developmental Medicine and Child Neurology|August 14, 2013
Two types of exercise-induced neuroplasticity in congenital hemiparesis: a transcranial magnetic stimulation, functional MRI, and magnetoencephalography studyHendrik Juenger, Nicola Kuhnke, Christoph Braun, et al.
Epilepsy Research|September 15, 2012
Etiology-specific differences in motor function after hemispherectomyNicolien M van der Kolk, Kim Boshuisen, Ron van Empelen, et al.
Epilepsia|November 6, 2021
Multilobar unilateral hypoplasia with emphasis on the posterior quadrant and severe epilepsy in children with FCD ILAE Type 1AHans Holthausen, Roland Coras, Yingying Tang, et al.
Neuropediatrics|March 3, 2015
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiencesAnna Biró, Ulrich Stephani, Tiziana Tarallo, et al.
American Journal of Medical Genetics. Part A|March 10, 2009
Prosaposin deficiency and saposin B deficiency (activator-deficient metachromatic leukodystrophy): report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutationsLadislav Kuchar, Jana Ledvinová, Martin Hrebícek, et al.
Nature Medicine|April 22, 2025
Antisense oligonucleotide treatment in a preterm infant with early-onset SCN2A developmental and epileptic encephalopathyMatias Wagner, Géza Berecki, Walid Fazeli, 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.
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