Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Katharina Vill

Showing results (1-10 of 85) with videos related to

Pageof 9
Sort By:
Neuropediatrics|June 20, 2017
Clinical Neurophysiology in Neuromuscular Disorders: Old Fashioned or Still Relevant?Wolfgang Müller-Felber, Katharina Vill
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 17, 2020
[Molecular therapies in childhood neuromuscular disorders-definite hope versus unknown pitfalls]Astrid Blaschek, Katharina Vill, Wolfgang Müller-Felber, et al.
Neuropediatrics|September 30, 2014
Overlap phenotype between CMT1A and hereditary neuropathy with liability to pressure palsies caused by the novel small in-frame deletion c.407_418del12 in PMP22 geneKatharina Vill, Marius Kuhn, Dieter Gläser, et al.
Neuropediatrics|November 9, 2013
Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategiesWolfgang Muller-Felber, Julia Wanschitz, Katharina Vill, et al.
Neuropediatrics|June 26, 2015
Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 GeneKatharina Vill, Marius Kuhn, Dieter Gläser, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2015
Six-minute walk test versus two-minute walk test in children with Duchenne muscular dystrophy: Is more time more information?Katharina Vill, Lena Ille, Sebastian A Schroeder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 12, 2024
Cortical impairment and reduced muscle mass in children and young adults with nephropathic cystinosisSusanne Bechtold-Dalla Pozza, Simon Lemster, Nadine Herzig, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 12, 2017
Corrigendum to "EEG changes in rolandic epilepsy under treatment with Levetiracetam and Sulthiame" [Eur J Paediatr Neurol 21 (Suppl. 1) (June 2017) e97]Moritz Tacke, Ingo Borggraefe, Lucia Gerstl, et al.
Parkinsonism & Related Disorders|February 25, 2023
TAOK1-related neurodevelopmental disorder: A new differential diagnosis for childhood-onset tremor?Astrid Blaschek, Alexandra Sitzberger, Melanie Brugger, et al.
Scientific Reports|March 18, 2022
Effects of a reduction of the number of electrodes in the EEG montage on the number of identified seizure patternsMoritz Tacke, Katharina Janson, Katharina Vill, et al.
Pageof 9

Showing results (1-10 of 85) with videos related to

Sort By:
Pageof 9
Neuropediatrics|June 20, 2017
Clinical Neurophysiology in Neuromuscular Disorders: Old Fashioned or Still Relevant?Wolfgang Müller-Felber, Katharina Vill
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|June 17, 2020
[Molecular therapies in childhood neuromuscular disorders-definite hope versus unknown pitfalls]Astrid Blaschek, Katharina Vill, Wolfgang Müller-Felber, et al.
Neuropediatrics|September 30, 2014
Overlap phenotype between CMT1A and hereditary neuropathy with liability to pressure palsies caused by the novel small in-frame deletion c.407_418del12 in PMP22 geneKatharina Vill, Marius Kuhn, Dieter Gläser, et al.
Neuropediatrics|November 9, 2013
Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategiesWolfgang Muller-Felber, Julia Wanschitz, Katharina Vill, et al.
Neuropediatrics|June 26, 2015
Long-Term Observations in an Affected Family with Neurogenic Scapuloperoneal Syndrome Caused by Mutation R269C in the TRPV4 GeneKatharina Vill, Marius Kuhn, Dieter Gläser, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 13, 2015
Six-minute walk test versus two-minute walk test in children with Duchenne muscular dystrophy: Is more time more information?Katharina Vill, Lena Ille, Sebastian A Schroeder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 12, 2024
Cortical impairment and reduced muscle mass in children and young adults with nephropathic cystinosisSusanne Bechtold-Dalla Pozza, Simon Lemster, Nadine Herzig, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 12, 2017
Corrigendum to "EEG changes in rolandic epilepsy under treatment with Levetiracetam and Sulthiame" [Eur J Paediatr Neurol 21 (Suppl. 1) (June 2017) e97]Moritz Tacke, Ingo Borggraefe, Lucia Gerstl, et al.
Parkinsonism & Related Disorders|February 25, 2023
TAOK1-related neurodevelopmental disorder: A new differential diagnosis for childhood-onset tremor?Astrid Blaschek, Alexandra Sitzberger, Melanie Brugger, et al.
Scientific Reports|March 18, 2022
Effects of a reduction of the number of electrodes in the EEG montage on the number of identified seizure patternsMoritz Tacke, Katharina Janson, Katharina Vill, et al.
Pageof 9