Jeannette Gelauff

ORCID: 0000-0001-6639-6771
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About
Contact & Profiles
Research Areas
  • Psychosomatic Disorders and Their Treatments
  • Neurological disorders and treatments
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Obsessive-Compulsive Spectrum Disorders
  • Genetic Neurodegenerative Diseases
  • Mental Health and Psychiatry
  • Botulinum Toxin and Related Neurological Disorders
  • Parkinson's Disease Mechanisms and Treatments
  • Glycogen Storage Diseases and Myoclonus
  • Body Image and Dysmorphia Studies
  • Neurology and Historical Studies
  • Neurological and metabolic disorders
  • Traumatic Brain Injury Research
  • Functional Brain Connectivity Studies
  • Neural and Behavioral Psychology Studies
  • Restless Legs Syndrome Research
  • Dementia and Cognitive Impairment Research
  • Attention Deficit Hyperactivity Disorder
  • Diet and metabolism studies
  • Tryptophan and brain disorders
  • Circadian rhythm and melatonin
  • Mental Health Research Topics
  • Neuroethics, Human Enhancement, Biomedical Innovations
  • Long-Term Effects of COVID-19
  • Genetics and Neurodevelopmental Disorders

Amsterdam University Medical Centers
2021-2024

Vrije Universiteit Amsterdam
2021-2024

University Medical Center Groningen
2014-2023

University of Groningen
2014-2023

University of Amsterdam
2011-2022

Amsterdam Neuroscience
2022

University of Edinburgh
2013-2020

St George's, University of London
2020

Fonds Psychische Gezondheid
2020

Cardiff University
2018

Abstract Reliable data on the prognosis of functional motor disorder are scarce, as existing studies nearly all retrospective, small and uncontrolled. In this study we used a prospectively recruited, controlled cohort design to assess misdiagnosis, mortality symptomatic health outcome in patients with limb weakness compared neurological disease healthy control subjects. We also carried out an exploratory analysis for baseline factors predicting outcome. One hundred seven weakness, 46 38...

10.1093/brain/awz138 article EN cc-by-nc Brain 2019-05-03

10.1007/s11940-014-0286-5 article EN Current Treatment Options in Neurology 2014-02-24

<h3>Objective</h3> To determine the contribution of electrophysiologic testing in diagnosis and anatomical classification myoclonus. <h3>Methods</h3> Participants with a clinical myoclonus were prospectively recruited, each undergoing videotaped examination battery tests. The its subtype was reviewed after 6 months context findings specialist review examination. <h3>Results</h3> Seventy-two patients recruited. Initial included 25 cortical myoclonus, 7 subcortical 2 spinal 15 functional...

10.1212/wnl.0000000000004996 article EN cc-by Neurology 2018-01-19

North Sea Progressive Myoclonus Epilepsy is a rare and severe disorder caused by mutations in the GOSR2 gene. It clinically characterized progressive myoclonus, seizures, early-onset ataxia areflexia. As other myoclonus epilepsies, efficacy of antiepileptic drugs disappointingly limited Epilepsy. The ketogenic diet less restrictive modified Atkins have been proven to be effective drug-resistant epilepsy syndromes, including those with myoclonic seizures. Our aim was evaluate patients...

10.1186/s13023-017-0595-3 article EN cc-by Orphanet Journal of Rare Diseases 2017-03-07

Functional neurological disorder (FND) is a common and disabling condition at the intersection of neurology psychiatry. Despite remarkable progress over recent decades, mechanisms FND are still poorly understood there limited diagnostic tools effective treatments. One potentially promising treatment modality for virtual reality (VR), which has been increasingly applied to broad range conditions, including neuropsychiatric disorders. unique features, many suggest particular relevance for,...

10.1136/bmjno-2023-000622 article EN cc-by-nc-nd BMJ Neurology Open 2024-07-01

Objective To study the effect of botulinum neurotoxin (BoNT) treatment in jerky and tremulous functional movement disorders (FMD). Methods Patients with invalidating, chronic (&gt;1 year) symptoms were randomly assigned to two subsequent treatments BoNT or placebo every 3 months stratification according symptom localisation. Improvement on dichotomised Clinical Global Impression-Improvement scale (CGI-I) (improvement vs no change worsening) at 4 months, assessed by investigators blinded...

10.1136/jnnp-2018-320071 article EN cc-by-nc Journal of Neurology Neurosurgery & Psychiatry 2019-06-20

To determine whether self-rated health of patients with motor functional neurologic disorder (FND) can be improved by unguided Internet-based self-help and education.In this nonblinded randomized controlled trial, were allocated 1:1 unbiased to an education website in addition usual care or only. Patients over 17 years age a symptom that caused distress disability included. The primary outcome was on the Clinical Global Improvement scale at 3 6 months. Secondary outcomes severity symptoms,...

10.1212/wnl.0000000000010381 article EN Neurology 2020-07-21

This exploratory study set out to investigate dynamic functional connectivity (dFC) in patients with jerky and tremulous movement disorders (JT-FMD). The focus this work is on brain states, which represent distinct dFC patterns that reoccur time across subjects. Resting-state fMRI data were collected from 17 JT-FMD healthy controls (HC). Symptom severity was measured using the Clinical Global Impression-Severity scale. Depression anxiety Beck Inventory (BDI) Anxiety (BAI), respectively....

10.1016/j.nicl.2020.102381 article EN cc-by NeuroImage Clinical 2020-01-01

Functional neurological disorder (FND) is a common and disabling condition at the intersection of neurology psychiatry. Despite remarkable progress over recent decades, mechanisms FND are still poorly understood there limited diagnostic tools effective treatments. One potentially promising treatment modality for virtual reality (VR), which has been increasingly applied to broad range conditions, including neuropsychiatric disorders. unique features, many suggest particular relevance for,...

10.31234/osf.io/xjurc preprint EN 2024-01-05

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10.2139/ssrn.4796044 preprint EN 2024-01-01
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