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Auteur de Visser M
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Visser (de) M
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Documents disponibles écrits par cet auteur



Revue : Neuromuscular disorders : NMD, 31, 1 Titre : Dysphagia in adult myopathies Type de document : Article Auteurs : Argov Z ; de Visser M Editeur : England Année de publication : 01/2021 Pages : p 5 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33334661 / DOI : 10.1016/j.nmd.2020.11.001
N° Profil MNM : 2020122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33334661 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Rheumatology (Oxford, England) Titre : Intravenous immunoglobulins as first-line treatment in idiopathic inflammatory myopathies: a pilot study Type de document : Article Auteurs : Lim J ; Eftimov F ; Verhamme C ; Brusse E ; Hoogendijk JE ; Saris CGJ ; Raaphorst J ; De Haan RJ ; van Schaik IN ; Aronica E ; de Visser M ; van der Kooi AJ Editeur : England Année de publication : 25/10/2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 33099648 / DOI : 10.1093/rheumatology/keaa459
N° Profil MNM : 2020102 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/33099648 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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Diagnostic accuracy of MRI and ultrasound in chronic immune-mediated neuropathies
Oudeman J, Eftimov F, Strijkers GJ, et al.
Neurology, 2020, 94, 1
Revue : Neurology, 94, 1 Titre : Diagnostic accuracy of MRI and ultrasound in chronic immune-mediated neuropathies Type de document : Article Auteurs : Oudeman J ; Eftimov F ; Strijkers GJ ; Schneiders JJ ; Roosendaal SD ; Engbersen MP ; Froeling M ; Goedee HS ; van Doorn PA ; Caan MWA ; van Schaik IN ; Maas M ; Nederveen AJ ; de Visser M ; Verhamme C Editeur : United States Année de publication : 01/2020 Langues : Anglais (eng) Mots-clés : amyotrophie spinale ; diagnostic différentiel ; étude de cohorte ; imagerie médicale ; maladie du motoneurone ; maladie du système nerveux périphérique ; neuropathie motrice multifocale ; polyradiculonévrite inflammatoire démyélinisante chronique Pubmed / DOI : Pubmed : 31827006 / DOI : 10.1212/WNL.0000000000008697
N° Profil MNM : 2019122 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/31827006 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
Revue : Neurology, 95, 11 Titre : The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series Type de document : Article Auteurs : Villar-Quiles RN ; von der Hagen M ; Metay C ; Gonzalez V ; Donkervoort S ; Bertini E ; Castiglioni C ; Chaigne D ; Colomer J ; Cuadrado ML ; de Visser M ; Desguerre I ; Eymard B ; Goemans N ; Kaindl A ; Lagrue E ; Lütschg J ; Malfatti E ; Mayer M ; Merlini L ; Orlikowski D ; Reuner U ; Salih MA ; Schlotter-Weigel B ; Stoetter M ; Straub V ; Topaloglu H ; Urtizberea JA ; van der Kooi A ; Wilichowski E ; Romero NB ; Fardeau M ; Bonnemann CG ; Estournet B ; Richard P ; Quijano-Roy S ; Schara U ; Ferreiro A Editeur : United States Année de publication : 2020 Langues : Anglais (eng) Pubmed / DOI : Pubmed : 32796131 / DOI : 10.1212/WNL.0000000000010327
N° Profil MNM : 2020081 En ligne : http://www.ncbi.nlm.nih.gov/pubmed/32796131 Avis des lecteurs Aucun avis, ajoutez le vôtre !
(mauvais) 15 (excellent)
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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
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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
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Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy reading
Olivier PA, de Paepe B, Aronica E, et al.
Neurology, 2019, 93, 9
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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
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Autoantibody testing in idiopathic inflammatory myopathies
Rietveld A, Lim J, de Visser M, et al.
Practical Neurology, 2019
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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
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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
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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
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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
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Le Centre neuromusculaire des Pays-Bas
Voermans N, Padberg G, Visser (de) M, et al.
Les Cahiers de Myologie, 2018, 17, p 35
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Classification of myositis
Lundberg IE, de Visser M, Werth VP
Nature reviews. Rheumatology, 2018, 14, 5, p 269
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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
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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
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Palliative care in neuromuscular diseases
de Visser M, Oliver DJ
Current opinion in neurology, 2017, 30, 6, p 686
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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
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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
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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
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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
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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
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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
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