about
Dystonia in children and adolescents: a systematic review and a new diagnostic algorithm.A novel diagnostic approach to patients with myoclonus.Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment.The efficacy of the modified Atkins diet in North Sea Progressive Myoclonus Epilepsy: an observational prospective open-label study.A post hoc study on gene panel analysis for the diagnosis of dystonia.Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation.Crossing barriers: a multidisciplinary approach to children and adults with young-onset movement disorders.Efficacy of hematopoietic cell transplantation in metachromatic leukodystrophy: the Dutch experience.Diaphragmatic weakness caused by neuroborreliosis.Ramsay Hunt syndrome: clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation.Improvement of White Matter Changes on Neuroimaging Modalities After Stem Cell Transplant in Metachromatic LeukodystrophyToward adaptive deep brain stimulation for dystonia[A toddler with vomiting and abnormal eye movements]Non-motor effects of deep brain stimulation in dystonia: A systematic reviewVariable Interpretation of the Dystonia Consensus Classification Items Compromises Its Solidity
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Martje E van Egmond
@ast
Martje E van Egmond
@en
Martje E van Egmond
@es
Martje E van Egmond
@nl
type
label
Martje E van Egmond
@ast
Martje E van Egmond
@en
Martje E van Egmond
@es
Martje E van Egmond
@nl
prefLabel
Martje E van Egmond
@ast
Martje E van Egmond
@en
Martje E van Egmond
@es
Martje E van Egmond
@nl
P106
P31
P496
0000-0003-2648-6937