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Neuropediatrics
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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 gene
Katharina Vill, Marius Kuhn, Dieter Gläser, et al.
Neuropediatrics
|
November 9, 2013
Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategies
Wolfgang 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 Gene
Katharina 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 cystinosis
Susanne 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 patterns
Moritz Tacke, Katharina Janson, Katharina Vill, et al.
Page
of 9
Search research articles
Search
Showing results (1-10 of 85) with videos related to
Sort By:
Page
of 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 gene
Katharina Vill, Marius Kuhn, Dieter Gläser, et al.
Neuropediatrics
|
November 9, 2013
Pediatric idiopathic inflammatory myopathies: an update on diagnostic and treatment strategies
Wolfgang 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 Gene
Katharina 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 cystinosis
Susanne 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 patterns
Moritz Tacke, Katharina Janson, Katharina Vill, et al.
Page
of 9