Search Results - "Verschuuren, Jan"

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  1. 1

    Myasthenia gravis: subgroup classification and therapeutic strategies by Gilhus, Nils Erik, Prof, Verschuuren, Jan J, Prof

    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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    Journal Article
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    Myasthenia gravis by Gilhus, Nils Erik, Tzartos, Socrates, Evoli, Amelia, Palace, Jacqueline, Burns, Ted M., Verschuuren, Jan J. G. M.

    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. 3

    Population-based incidence and prevalence of facioscapulohumeral dystrophy by Deenen, Johanna C.W, Arnts, Hisse, van der Maarel, Silvère M, Padberg, George W, Verschuuren, Jan J.G.M, Bakker, Egbert, Weinreich, Stephanie S, Verbeek, André L.M, van Engelen, Baziel G.M

    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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    Lambert–Eaton myasthenic syndrome: from clinical characteristics to therapeutic strategies by Titulaer, Maarten J, Dr, Lang, Bethan, PhD, Verschuuren, Jan JGM, Prof

    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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    A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities by Cox, Fieke M., Titulaer, Maarten J., Sont, Jacob K., Wintzen, Axel R., Verschuuren, Jan J. G. M., Badrising, Umesh A.

    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 by Boldingh, Marion I, Maniaol, Angelina H, Brunborg, Cathrine, Weedon-Fekjær, Harald, Verschuuren, Jan J.G.M, Tallaksen, Chantal M.E

    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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  9. 9

    Fatigue in patients with myasthenia gravis. A systematic review of the literature by Ruiter, Annabel M., Verschuuren, Jan J.G.M., Tannemaat, Martijn R.

    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 by Verschuuren, Jan JGM, Palace, Jacqueline, Murai, Hiroyuki, Tannemaat, Martijn R, Kaminski, Henry J, Bril, Vera

    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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    Emerging therapies for autoimmune myasthenia gravis: Towards treatment without corticosteroids by Tannemaat, Martijn R., Verschuuren, Jan J.G.M.

    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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    Improved olefinic fat suppression in skeletal muscle DTI using a magnitude‐based dixon method by Burakiewicz, Jedrzej, Hooijmans, Melissa T., Webb, Andrew G., Verschuuren, Jan J.G.M., Niks, Erik H., Kan, Hermien E.

    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 by Remijn-Nelissen, Linda, Verschuuren, Jan J.G.M., Tannemaat, Martijn R.

    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 by Hooijmans, Melissa T., Froeling, Martijn, Koeks, Zaida, Verschuuren, Jan J.G.M., Webb, Andrew, Niks, Erik H., Kan, Hermien E.

    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 by Ruiter, Annabel M., Verschuuren, Jan J.G.M., Tannemaat, Martijn R.

    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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    Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models by van der Pijl, Elizabeth M., van Putten, Maaike, Niks, Erik H., Verschuuren, Jan J. G. M., Aartsma-Rus, Annemieke, Plomp, Jaap J.

    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 by Lipka, Alexander F., Boldingh, Marion I., van Zwet, Erik W., Schreurs, Marco W.J., Kuks, Jan B.M., Tallaksen, Chantal M., Titulaer, Maarten J., Verschuuren, Jan J.G.M.

    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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