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Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study
Lim J, Eftimov F, Verhamme C, et al.
Rheumatology (Oxford, England), 2020
New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy
Alonso-Perez J, Gonzalez-Quereda L, Bello L, et al.
Brain : a journal of neurology, 2020, 143, 9, p 2696
Diagnostic accuracy of MRI and ultrasound in chronic immune-mediated neuropathies
Oudeman J, Eftimov F, Strijkers GJ, et al.
Neurology, 2020, 94, 1
The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series
Villar-Quiles RN, von der Hagen M, Metay C, et al.
Neurology, 2020, 95, 11
Assessing the content validity of patient-reported outcome measures in adult myositis: A report from the OMERACT myositis working group
Esfandiary T, Park JK, Alexanderson H, et al.
Seminars in arthritis and rheumatism, 2020, 50, 5, p 943
Safety and efficacy of intravenous bimagrumab in inclusion body myositis (RESILIENT): a randomised, double-blind, placebo-controlled phase 2b trial
Hanna MG, Badrising UA, Benveniste O, et al.
The Lancet. Neurology, 2019, 18, 9, p 834
Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy reading
Olivier PA, de Paepe B, Aronica E, et al.
Neurology, 2019, 93, 9
Galectin-9 and CXCL10 as biomarkers for disease activity in juvenile dermatomyositis: a longitudinal cohort study and multi-cohort validation
Wienke J, Bellutti Enders F, Lim J, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2019
Autoantibody testing in idiopathic inflammatory myopathies
Rietveld A, Lim J, de Visser M, et al.
Practical Neurology, 2019
OMERACT 2018 Modified Patient-reported Outcome Domain Core Set in the Life Impact Area for Adult Idiopathic Inflammatory Myopathies
Regardt M, Mecoli CA, Park JK, et al.
The Journal of rheumatology, 2019
Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients
Ten Dam L, Frankhuizen WS, Linssen WHJP, et al.
Clinical genetics, 2019, 96, 2, p 126
Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities
Weterman MAJ, Kuo M, Kenter SB, et al.
Human molecular genetics, 2018, 27, 23, p 4036
Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy.
Lim J, Rietveld A, De Bleecker JL, et al.
Neurology(R) neuroimmunology & neuroinflammation, 2018, e513
Le Centre neuromusculaire des Pays-Bas
Voermans N, Padberg G, Visser (de) M, et al.
Les Cahiers de Myologie, 2018, 17, p 35
Classification of myositis
Lundberg IE, de Visser M, Werth VP
Nature reviews. Rheumatology, 2018, 14, 5, p 269
2016 American College of Rheumatology/European League Against Rheumatism criteria for minimal, moderate, and major clinical response in adult dermatomyositis and polymyositis : An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative
Aggarwal R, Rider LG, Ruperto N, et al.
Annals of the rheumatic diseases, 2017, 76, 5, p 792
2016 American College of Rheumatology/European League Against Rheumatism Criteria for Minimal, Moderate, and Major Clinical Response in Adult Dermatomyositis and Polymyositis : An International Myositis Assessment and Clinical Studies Group/Paediatric Rheumatology International Trials Organisation Collaborative Initiative
Aggarwal R, Rider LG, Ruperto N, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2017, 69, 5, p 898
Palliative care in neuromuscular diseases
de Visser M, Oliver DJ
Current opinion in neurology, 2017, 30, 6, p 686
Muscle imaging in inherited and acquired muscle diseases
Ten Dam L, van der Kooi AJ, Verhamme C, et al.
European journal of neurology, 2016, 23, 4, p 688
Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USA
Price MA, Barghout V, Benveniste O, et al.
Journal of Neuromuscular Diseases, 2016, 3, 1, p 67
Myasthenia gravis with muscle specific kinase antibodies mimicking amyotrophic lateral sclerosis
Huijbers MG, Niks EH, Klooster R, et al.
Neuromuscular disorders : NMD, 2016, 26, 6, p 350
RYR1-related myopathies: a wide spectrum of phenotypes throughout life
Snoeck M, van Engelen BG, Küsters B, et al.
European journal of neurology : the official journal of the European Federation of Neurological Societies, 2015, 22, 7, p 1094
Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy
Scoto M, Rossor AM, Harms MB, et al.
Neurology, 2015, 84, 7, p 668
Pathology diagnosis of idiopathic inflammatory myopathies Part II : Actes de colloque - 205th ENMC International Workshop - 28-30 March 2014, Naarden The Netherlands
De Bleecker JL, de Paepe B, Aronica E, et al.
Neuromuscular disorders : NMD, 2015, 25, 3, p 268
