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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2015-03, Vol.25 (3), p.268-272

2015

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239th ENMC International Workshop: Classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018

Neuromuscular disorders : NMD, 2020-01, Vol.30 (1), p.70-92

2020

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Effect of efgartigimod on muscle group subdomains in participants with generalized myasthenia gravis: post hoc analyses of the phase 3 pivotal ADAPT study

European journal of neurology, 2024-01, Vol.31 (1), p.e16098-n/a

2024

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C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD

Acta neuropathologica, 2023-06, Vol.145 (6), p.793-814

2023

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Cytokines and Chemokines as Regulators of Skeletal Muscle Inflammation: Presenting the Case of Duchenne Muscular Dystrophy

Mediators of Inflammation, 2013-01, Vol.2013, p.540370-10

2013

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A Phase 3 Multicenter, Prospective, Open-Label Efficacy and Safety Study of Immune Globulin (Human) 10% Caprylate/Chromatography Purified in Patients with Myasthenia Gravis Exacerbations

European neurology, 2019-11, Vol.81 (5-6), p.223-230

2019

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Disease specificity of autoantibodies to cytosolic 5′-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases

Annals of the rheumatic diseases, 2016-04, Vol.75 (4), p.696-701

2016

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Description of a Novel Mechanism Possibly Explaining the Antiproliferative Properties of Glucocorticoids in Duchenne Muscular Dystrophy Fibroblasts Based on Glucocorticoid Receptor GR and NFAT5

International journal of molecular sciences, 2020-12, Vol.21 (23), p.9225

2020

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Anti-Inflammatory and General Glucocorticoid Physiology in Skeletal Muscles Affected by Duchenne Muscular Dystrophy: Exploration of Steroid-Sparing Agents

International journal of molecular sciences, 2020-06, Vol.21 (13), p.4596

2020

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Description of Osmolyte Pathways in Maturing Mdx Mice Reveals Altered Levels of Taurine and Sodium/Myo-Inositol Co-Transporters

International journal of molecular sciences, 2022-03, Vol.23 (6), p.3251

2022

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Exploring the Therapeutic Potential of Ectoine in Duchenne Muscular Dystrophy: Comparison with Taurine, a Supplement with Known Beneficial Effects in the mdx Mouse

International journal of molecular sciences, 2022-09, Vol.23 (17), p.9567

2022

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Expanding the TDP-43 Proteinopathy Pathway From Neurons to Muscle: Physiological and Pathophysiological Functions

Frontiers in neuroscience, 2022-02, Vol.16, p.815765

2022

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NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients

Neurobiology of aging, 2018-01, Vol.61, p.255.e1-255.e7

2018

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Retrospective Study Shows That Serum Levels of Chemokine CXCL10 and Cytokine GDF15 Support a Diagnosis of Sporadic Inclusion Body Myositis and Immune-Mediated Necrotizing Myopathy

Brain sciences, 2023-09, Vol.13 (10), p.1369

2023

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Role of cytokines and chemokines in idiopathic inflammatory myopathies

Current opinion in rheumatology, 2009-11, Vol.21 (6), p.610-616

2009

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A rare case of adult-onset spastic paraparesis associated with Klinefelter syndrome

BMC neurology, 2024-01, Vol.24 (1), p.29-29, Article 29

2024

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Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: Balancing muscle protection and destruction

Neuromuscular disorders : NMD, 2012-01, Vol.22 (1), p.26-33

2012

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193rd ENMC International workshop Pathology diagnosis of idiopathic inflammatory myopathies 30 November – 2 December 2012, Naarden, The Netherlands

Neuromuscular disorders : NMD, 2013-11, Vol.23 (11), p.945-951

2013

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Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy

Neurology : neuroimmunology & neuroinflammation, 2019-01, Vol.6 (1), p.e513-e513

2019

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Long-term safety, tolerability, and efficacy of efgartigimod (ADAPT+): interim results from a phase 3 open-label extension study in participants with generalized myasthenia gravis

Frontiers in neurology, 2024-01, Vol.14, p.1284444-1284444

2024

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The nonnecrotic invaded muscle fibers of polymyositis and sporadic inclusion body myositis: On the interplay of chemokines and stress proteins

Neuroscience letters, 2013-02, Vol.535, p.18-23

2013

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Myo-Inositol Transporter SLC5A3 Associates with Degenerative Changes and Inflammation in Sporadic Inclusion Body Myositis

Biomolecules (Basel, Switzerland), 2020-03, Vol.10 (4), p.521

2020

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205th ENMC International Workshop: Pathology diagnosis of idiopathic inflammatory myopathies Part II 28–30 March 2014, Naarden, The Netherlands

239th ENMC International Workshop: Classification of dermatomyositis, Amsterdam, the Netherlands, 14–16 December 2018

Effect of efgartigimod on muscle group subdomains in participants with generalized myasthenia gravis: post hoc analyses of the phase 3 pivotal ADAPT study

C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD

Cytokines and Chemokines as Regulators of Skeletal Muscle Inflammation: Presenting the Case of Duchenne Muscular Dystrophy

Loss of DPP6 in neurodegenerative dementia: a genetic player in the dysfunction of neuronal excitability

FAHN/SPG35: a narrow phenotypic spectrum across disease classifications

A Phase 3 Multicenter, Prospective, Open-Label Efficacy and Safety Study of Immune Globulin (Human) 10% Caprylate/Chromatography Purified in Patients with Myasthenia Gravis Exacerbations

Disease specificity of autoantibodies to cytosolic 5′-nucleotidase 1A in sporadic inclusion body myositis versus known autoimmune diseases

Description of a Novel Mechanism Possibly Explaining the Antiproliferative Properties of Glucocorticoids in Duchenne Muscular Dystrophy Fibroblasts Based on Glucocorticoid Receptor GR and NFAT5

Anti-Inflammatory and General Glucocorticoid Physiology in Skeletal Muscles Affected by Duchenne Muscular Dystrophy: Exploration of Steroid-Sparing Agents

Description of Osmolyte Pathways in Maturing Mdx Mice Reveals Altered Levels of Taurine and Sodium/Myo-Inositol Co-Transporters

Exploring the Therapeutic Potential of Ectoine in Duchenne Muscular Dystrophy: Comparison with Taurine, a Supplement with Known Beneficial Effects in the mdx Mouse

Expanding the TDP-43 Proteinopathy Pathway From Neurons to Muscle: Physiological and Pathophysiological Functions

NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients

Retrospective Study Shows That Serum Levels of Chemokine CXCL10 and Cytokine GDF15 Support a Diagnosis of Sporadic Inclusion Body Myositis and Immune-Mediated Necrotizing Myopathy

Role of cytokines and chemokines in idiopathic inflammatory myopathies

A rare case of adult-onset spastic paraparesis associated with Klinefelter syndrome

Heat shock protein families 70 and 90 in Duchenne muscular dystrophy and inflammatory myopathy: Balancing muscle protection and destruction

193rd ENMC International workshop Pathology diagnosis of idiopathic inflammatory myopathies 30 November – 2 December 2012, Naarden, The Netherlands

Seronegative patients form a distinctive subgroup of immune-mediated necrotizing myopathy

Long-term safety, tolerability, and efficacy of efgartigimod (ADAPT+): interim results from a phase 3 open-label extension study in participants with generalized myasthenia gravis

Response to: 'Antisynthetase syndrome or what else? Different perspectives indicate the need for new classification criteria' by Cavagna et al

The nonnecrotic invaded muscle fibers of polymyositis and sporadic inclusion body myositis: On the interplay of chemokines and stress proteins

Myo-Inositol Transporter SLC5A3 Associates with Degenerative Changes and Inflammation in Sporadic Inclusion Body Myositis

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