Hendriekje Eggink
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View article: Benign Idiopathic Myoclonus: A New Clinical Entity?
Benign Idiopathic Myoclonus: A New Clinical Entity? Open
Background Myoclonus is a brief shock‐like, involuntary movement, which can be distinguished in physiologic, essential, epileptic, and symptomatic, according to its etiology. Physiologic myoclonus typically occurs in healthy people without…
View article: Eye movement disorders in genetic dystonia syndromes: A literature overview
Eye movement disorders in genetic dystonia syndromes: A literature overview Open
With the growing possibilities in genetic testing, the number of genetic disorders associated with dystonia has constantly increased over the last few years. Accurate phenotyping is crucial to guide and interpret genetic analyses in the se…
View article: Intermuscular coherence during co-contraction eliciting tasks as a biomarker for dystonia and GPi-DBS efficacy
Intermuscular coherence during co-contraction eliciting tasks as a biomarker for dystonia and GPi-DBS efficacy Open
View article: Improving paediatric movement disorders care: Insights on rating scales utilization and clinical practice
Improving paediatric movement disorders care: Insights on rating scales utilization and clinical practice Open
View article: The natural history of progressive myoclonus ataxia
The natural history of progressive myoclonus ataxia Open
Progressive myoclonus ataxia (PMA) is a rare clinical syndrome characterized by the presence of progressive myoclonus and ataxia, and can be accompanied by mild cognitive impairment and infrequent epileptic seizures. This is the first stud…
View article: Moving across disorders: A cross-sectional study of cognition in early onset ataxia and dystonia
Moving across disorders: A cross-sectional study of cognition in early onset ataxia and dystonia Open
View article: <i>Taenia martis</i> Neurocysticercosis-Like Lesion in Child, Associated with Local Source, the Netherlands
<i>Taenia martis</i> Neurocysticercosis-Like Lesion in Child, Associated with Local Source, the Netherlands Open
A neurocysticercosis-like lesion in an 11-year-old boy in the Netherlands was determined to be caused by the zoonotic Taenia martis tapeworm. Subsequent testing revealed that 15% of wild martens tested in that region were infected with T. …
View article: Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review
Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review Open
View article: Deep brain stimulation in dystonia: The added value of neuropsychological assessments
Deep brain stimulation in dystonia: The added value of neuropsychological assessments Open
Deep brain stimulation (DBS) of the internal globus pallidus (GPi) is a recognized treatment for medication‐refractory dystonia. Problems in executive functions and social cognition can be part of dystonia phenotypes. The impact of pallida…
View article: Early Onset Dystonia: Complaints about Executive Functioning, Depression and Anxiety
Early Onset Dystonia: Complaints about Executive Functioning, Depression and Anxiety Open
Early Onset Dystonia (EOD) is thought to result from basal ganglia dysfunction, structures also involved in non-motor functions, like regulation of behavior, mood and anxiety. Problems in these domains have been found in proxy-reports but …
View article: Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review
Clinical Characteristics Suggestive of a Genetic Cause in Cerebral Palsy: A Systematic Review Open
View article: Cognition in children and young adults with myoclonus dystonia – A case control study
Cognition in children and young adults with myoclonus dystonia – A case control study Open
View article: The Effectiveness of Deep Brain Stimulation in Dystonia: A Patient-Centered Approach
The Effectiveness of Deep Brain Stimulation in Dystonia: A Patient-Centered Approach Open
Functional priorities in life of dystonia patients and their caregivers vary greatlyThe effect of DBS on functional priorities did not correlate with motor outcomeHalf of the motor 'non-responder' patients reported important changes in the…
View article: Moving forward in childhood-onset movement disorders: a multidisciplinary approach to diagnosis and care
Moving forward in childhood-onset movement disorders: a multidisciplinary approach to diagnosis and care Open
Eggink focused her research on movement disorders in children and young-adults, especially dystonia. Neurological movement disorders cause a disruption in the execution of movements or present with involuntary movements. The thesis is divi…
View article: Intermuscular coherence as biomarker for pallidal deep brain stimulation efficacy in dystonia
Intermuscular coherence as biomarker for pallidal deep brain stimulation efficacy in dystonia Open
View article: Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemia
Movement disorders and nonmotor neuropsychological symptoms in children and adults with classical galactosemia Open
Although movement disorders (MDs) are known complications, the exact frequency and severity remains uncertain in patients with classical galactosemia, especially in children. We determined the frequency, classification and severity of MDs …
View article: The neurological phenotype of developmental motor patterns during early childhood
The neurological phenotype of developmental motor patterns during early childhood Open
Introduction During early childhood, typical human motor behavior reveals a gradual transition from automatic motor patterns to acquired motor skills, by the continuous interplay between nature and nurture. During the wiring and shaping of…
View article: Motor and non-motor determinants of health-related quality of life in young dystonia patients
Motor and non-motor determinants of health-related quality of life in young dystonia patients Open
View article: Non-motor effects of deep brain stimulation in dystonia: A systematic review
Non-motor effects of deep brain stimulation in dystonia: A systematic review Open
View article: Crossing barriers: a multidisciplinary approach to children and adults with young-onset movement disorders
Crossing barriers: a multidisciplinary approach to children and adults with young-onset movement disorders Open
View article: Reversal of Status Dystonicus after Relocation of Pallidal Electrodes in DYT6 Generalized Dystonia
Reversal of Status Dystonicus after Relocation of Pallidal Electrodes in DYT6 Generalized Dystonia Open
Background: DYT6 dystonia can have an unpredictable clinical course and the result of deep brain stimulation (DBS) of the internal part of the globus pallidus (GPi) is known to be less robust than in other forms of autosomal dominant dysto…
View article: Cognition in childhood dystonia: a systematic review
Cognition in childhood dystonia: a systematic review Open
Aim Cognitive impairments have been established as part of the non‐motor phenomenology of adult dystonia. In childhood dystonia, the extent of cognitive impairments is less clear. This systematic review aims to present an overview of the e…
View article: Reversal of Status Dystonicus after Relocation of Pallidal Electrodes in DYT6 Generalized Dystonia
Reversal of Status Dystonicus after Relocation of Pallidal Electrodes in DYT6 Generalized Dystonia Open
Background: DYT6 dystonia can have an unpredictable clinical course and the result of deep brain stimulation (DBS) of the internal part of the globus pallidus (GPi) is known to be less robust than in other forms of autosomal dominant dysto…
View article: Response to ‘Classification of cerebral palsy and potential role of video recording’
Response to ‘Classification of cerebral palsy and potential role of video recording’ Open
View article: Spasticity, dyskinesia and ataxia in cerebral palsy: Are we sure we can differentiate them?
Spasticity, dyskinesia and ataxia in cerebral palsy: Are we sure we can differentiate them? Open
View article: Dystonia‐deafness syndrome caused by a β‐actin gene mutation and response to deep brain stimulation
Dystonia‐deafness syndrome caused by a β‐actin gene mutation and response to deep brain stimulation Open
Introduction Dystonia‐deafness syndrome is a distinct clinical presentation within the dystonia‐spectrum. Although several genetic and acquired causes have been reported, etiology remains unknown in the majority of patients. Objectives To …
View article: Neurometabolic disorders are treatable causes of dystonia
Neurometabolic disorders are treatable causes of dystonia Open
View article: Clinical Scores for Dyspnoea Severity in Children: A Prospective Validation Study
Clinical Scores for Dyspnoea Severity in Children: A Prospective Validation Study Open
This study shows that commonly used dyspnoea scores show insufficient validity and reliability to allow for clinical use without caution.
View article: Teaching Video Neuro <i>Images</i> : The “round the houses” sign as a clinical clue for Niemann-Pick disease type C
Teaching Video Neuro <i>Images</i> : The “round the houses” sign as a clinical clue for Niemann-Pick disease type C Open
A 58-year-old man presented with progressive involuntary jerky movements. In addition to a cortical myoclonus, supported by polymyographic evaluation, we saw a "looping" trajectory of the vertical saccades, also referred to as the "round t…
View article: The Burke‐Fahn‐Marsden Dystonia Rating Scale is Age‐Dependent in Healthy Children
The Burke‐Fahn‐Marsden Dystonia Rating Scale is Age‐Dependent in Healthy Children Open
View Supplementary Video 1 Background The Burke‐Fahn‐Marsden Dystonia Rating Scale is a universally applied instrument for the quantitative assessment of dystonia in both children and adults. However, immature movements by healthy young ch…