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Doing it Wrong: A Systematic Review on Electrocortical and Behavioral Correlates of Error Monitoring in Patients with Neurological Disorders

Neuroscience, 2022-03, Vol.486, p.103-125

2022

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Opposing dorsal/ventral stream dynamics during figure-ground segregation

Journal of vision (Charlottesville, Va.), 2013-07, Vol.13 (9), p.1260-1260

2013

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Figure-ground signals in early and object specific visual areas: A combined fMRI, EEG and rTMS study

Journal of vision (Charlottesville, Va.), 2010-08, Vol.10 (7), p.1218-1218

2010

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The clinical spectrum and incidence of anti-MOG-associated acquired demyelinating syndromes in children and adults

Multiple sclerosis, 2020-06, Vol.26 (7), p.806-814

2020

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Quantitative MRI and strength measurements in the assessment of muscle quality in Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2014-05, Vol.24 (5), p.409-416

2014

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Multidisciplinary ALS care improves quality of life in patients with ALS

Neurology, 2005-10, Vol.65 (8), p.1264-1267

2005

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Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

Neurology, 2008-11, Vol.71 (19), p.1500-1505

2008

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Long-term outcome in polymyositis and dermatomyositis

Annals of the rheumatic diseases, 2006-11, Vol.65 (11), p.1456-1461

2006

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Trends and determinants of end-of-life practices in ALS in the Netherlands

Neurology, 2009-09, Vol.73 (12), p.954-961

2009

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Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study

Brain (London, England : 1878), 2008-05, Vol.131 (5), p.1217-1227

2008

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Prospective trial of natalizumab personalised extended interval dosing by therapeutic drug monitoring in relapsing-remitting multiple sclerosis (NEXT-MS)

Journal of neurology, neurosurgery and psychiatry, 2024-05, Vol.95 (5), p.392-400

2024

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Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis

Annals of neurology, 2009-08, Vol.66 (2), p.227-234

2009

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Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

Neurology, 2010-08, Vol.75 (9), p.818-825

2010

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Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease

Neuromuscular disorders : NMD, 2009-02, Vol.19 (2), p.113-117

2009

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Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2007-04, Vol.78 (4), p.367-371

2007

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Dystrophin levels and clinical severity in Becker muscular dystrophy patients

Journal of neurology, neurosurgery and psychiatry, 2014-07, Vol.85 (7), p.747-753

2014

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HLA association in MOG-IgG– and AQP4-IgG–related disorders of the CNS in the Dutch population

Neurology : neuroimmunology & neuroinflammation, 2020-05, Vol.7 (3), p.e702-e702

2020

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Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study

Orphanet journal of rare diseases, 2012-11, Vol.7 (1), p.88-88

2012

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Benefits of sphingosine-1-phosphate receptor modulators in relapsing MS estimated with a treatment sequence model

Multiple sclerosis and related disorders, 2023-12, Vol.80, p.105100-105100, Article 105100

2023

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Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Neurology, 2007-06, Vol.68 (24), p.2125-2128

2007

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Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis

Brain (London, England : 1878), 2005-10, Vol.128 (10), p.2327-2337

2005

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Drug treatment for spinal muscular atrophy types II and III

Cochrane database of systematic reviews, 2012-04 (4), p.CD006282

2012

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Polymyositis: an overdiagnosed entity

Neurology, 2003-08, Vol.61 (3), p.316-321

2003

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Sexual differences in onset of disease and response to exercise in a transgenic model of ALS

Neuromuscular disorders : NMD, 2003-11, Vol.13 (9), p.737-743

2003

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Decreased cerebral perfusion in Duchenne muscular dystrophy patients

Neuromuscular disorders : NMD, 2017-01, Vol.27 (1), p.29-37

2017

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Doing it Wrong: A Systematic Review on Electrocortical and Behavioral Correlates of Error Monitoring in Patients with Neurological Disorders

Opposing dorsal/ventral stream dynamics during figure-ground segregation

Figure-ground signals in early and object specific visual areas: A combined fMRI, EEG and rTMS study

The clinical spectrum and incidence of anti-MOG-associated acquired demyelinating syndromes in children and adults

Quantitative MRI and strength measurements in the assessment of muscle quality in Duchenne muscular dystrophy

Multidisciplinary ALS care improves quality of life in patients with ALS

Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes

Long-term outcome in polymyositis and dermatomyositis

Trends and determinants of end-of-life practices in ALS in the Netherlands

Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype–phenotype correlation study

Prospective trial of natalizumab personalised extended interval dosing by therapeutic drug monitoring in relapsing-remitting multiple sclerosis (NEXT-MS)

Randomized sequential trial of valproic acid in amyotrophic lateral sclerosis

Correlates of outcome and response to IVIg in 88 patients with multifocal motor neuropathy

Rate of disease progression during long-term follow-up of patients with late-onset Pompe disease

Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis

Dystrophin levels and clinical severity in Becker muscular dystrophy patients

HLA association in MOG-IgG– and AQP4-IgG–related disorders of the CNS in the Dutch population

Clinical features and predictors for disease natural progression in adults with Pompe disease: a nationwide prospective observational study

Benefits of sphingosine-1-phosphate receptor modulators in relapsing MS estimated with a treatment sequence model

Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Increased expression of rapsyn in muscles prevents acetylcholine receptor loss in experimental autoimmune myasthenia gravis

Drug treatment for spinal muscular atrophy types II and III

Polymyositis: an overdiagnosed entity

Sexual differences in onset of disease and response to exercise in a transgenic model of ALS

Decreased cerebral perfusion in Duchenne muscular dystrophy patients

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