Search Results - "Verschuuren, Jan"
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Myasthenia gravis: subgroup classification and therapeutic strategies
Published in Lancet neurology (01-10-2015)“…Summary Myasthenia gravis is an autoimmune disease that is characterised by muscle weakness and fatigue, is B-cell mediated, and is associated with antibodies…”
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Myasthenia gravis
Published in Nature reviews. Disease primers (02-05-2019)“…Myasthenia gravis (MG) is an autoimmune disease caused by antibodies against the acetylcholine receptor (AChR), muscle-specific kinase (MuSK) or other…”
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3
Population-based incidence and prevalence of facioscapulohumeral dystrophy
Published in Neurology (16-09-2014)“…OBJECTIVE:To determine the incidence and prevalence of facioscapulohumeral muscular dystrophy (FSHD) in the Netherlands. METHODS:Using 3-source…”
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4
Lambert–Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies
Published in Lancet neurology (01-12-2011)“…Summary Lambert–Eaton myasthenic syndrome (LEMS) is a neuromuscular autoimmune disease that has served as a model for autoimmunity and tumour immunology. In…”
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Pathophysiology of myasthenia gravis with antibodies to the acetylcholine receptor, muscle-specific kinase and low-density lipoprotein receptor-related protein 4
Published in Autoimmunity reviews (01-07-2013)“…Abstract Myasthenia gravis is caused by antibodies to the acetylcholine receptor, muscle-specific kinase, low-density lipoprotein receptor-related protein 4,…”
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6
Randomized phase 2 study of FcRn antagonist efgartigimod in generalized myasthenia gravis
Published in Neurology (04-06-2019)“…OBJECTIVETo investigate safety and explore efficacy of efgartigimod (ARGX-113), an anti-neonatal Fc receptor immunoglobulin G1 Fc fragment, in patients with…”
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7
A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities
Published in Brain (London, England : 1878) (01-11-2011)“…Sporadic inclusion body myositis is considered to be a slowly progressive myopathy. Long-term follow-up data are, however, not yet available. Follow-up data…”
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Increased risk for clinical onset of myasthenia gravis during the postpartum period
Published in Neurology (15-11-2016)“…OBJECTIVE:To study the risk of clinical onset of myasthenia gravis (MG) in pregnancy and during the first 6 months postpartum because an association between…”
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Fatigue in patients with myasthenia gravis. A systematic review of the literature
Published in Neuromuscular disorders : NMD (01-08-2020)“…•Central fatigue is highly prevalent in autoimmune Myasthenia Gravis.•There is a strong association with disease severity, female gender and depressive…”
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Advances and ongoing research in the treatment of autoimmune neuromuscular junction disorders
Published in Lancet neurology (01-02-2022)“…Myasthenia gravis and Lambert-Eaton myasthenic syndrome are antibody-mediated autoimmune diseases of the neuromuscular junction that usually present with…”
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Efgartigimod improved health-related quality of life in generalized myasthenia gravis: results from a randomized, double-blind, placebo-controlled, phase 3 study (ADAPT)
Published in Journal of neurology (01-04-2023)“…There are substantial disease and health-related quality-of-life (HRQoL) burdens for many patients with myasthenia gravis (MG), especially for those whose…”
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Emerging therapies for autoimmune myasthenia gravis: Towards treatment without corticosteroids
Published in Neuromuscular disorders : NMD (01-02-2020)“…•Prednisolone, the mainstay of treatment for MG, has major adverse effects on long term health.•Several drug trials have failed, possibly due to suboptimal…”
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Timing and localization of human dystrophin isoform expression provide insights into the cognitive phenotype of Duchenne muscular dystrophy
Published in Scientific reports (03-10-2017)“…Duchenne muscular dystrophy (DMD) is a muscular dystrophy with high incidence of learning and behavioural problems and is associated with neurodevelopmental…”
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14
Improved olefinic fat suppression in skeletal muscle DTI using a magnitude‐based dixon method
Published in Magnetic resonance in medicine (01-01-2018)“…Purpose To develop a method of suppressing the multi‐resonance fat signal in diffusion‐weighted imaging of skeletal muscle. This is particularly important when…”
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The effectiveness and side effects of pyridostigmine in the treatment of myasthenia gravis: a cross-sectional study
Published in Neuromuscular disorders : NMD (01-10-2022)“…•The net benefit and effectiveness of pyridostigmine are moderate.•A quarter of all patients report side effects as the main reason to discontinue…”
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Multi‐parametric MR in Becker muscular dystrophy patients
Published in NMR in biomedicine (01-11-2020)“…Quantitative MRI and MRS of muscle are increasingly being used to measure individual pathophysiological processes in Becker muscular dystrophy (BMD). In…”
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Prevalence and associated factors of fatigue in autoimmune myasthenia gravis
Published in Neuromuscular disorders : NMD (01-07-2021)“…•Fatigue is highly prevalent and increases with disease severity.•Quality of life decreases rapidly as fatigue increases.•Coping strategies differ between…”
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Updated Diagnostic Criteria for Paraneoplastic Neurologic Syndromes
Published in Neurology : neuroimmunology & neuroinflammation (01-07-2021)“…The contemporary diagnosis of paraneoplastic neurologic syndromes (PNSs) requires an increasing understanding of their clinical, immunologic, and oncologic…”
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Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models
Published in The European journal of neuroscience (01-06-2016)“…Duchenne muscular dystrophy (DMD) is an X‐linked myopathy caused by dystrophin deficiency. Dystrophin is present intracellularly at the sarcolemma, connecting…”
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Long‐term follow‐up, quality of life, and survival of patients with Lambert‐Eaton myasthenic syndrome
Published in Neurology (04-02-2020)“…OBJECTIVETo study survival and to characterize long-term functional impairments and health-related quality of life (HRQOL) of patients with Lambert-Eaton…”
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