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Efficacy of efgartigimod in generalized myasthenia gravis : myasthenia gravis composite score analysis from ADAPT
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S82-S83 -
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A structural variant of the C-terminal prion-like domain of TDP-43 causes vacuolar muscle degeneration
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S119-S119 -
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Two-years prospective natural history study in 24 adult LGMDR12 patients : clinical and radiological outcome measures
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S170-S171 -
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Hematological effects of intravenous immunoglobulin therapy in patients with neuromuscular diseases : a retrospective analysis
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S226-S227 -
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Belgian retrospective survey of hereditary transthyretin-mediated (hATTR) amyloidosis patients treated with patisiran in real-world practice
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S273-S274 -
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Risk of malignant hyperthermia in patients carrying a variant in the ryanodine receptor 1 gene
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S296-S296 -
- Conference Paper
- C3
- open access
Description of osmolyte pathways in maturing MDX mice reveals altered taurine and sodium/myo-inositol co-transporter levels
(2022) JOURNAL OF NEUROMUSCULAR DISEASES. In Journal of Neuromuscular Diseases 9(supplement 1). p.S302-S302 -
Het ‘three territory sign’ als een merker van occulte maligniteit bij een beroerte
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Advance care planning in amyotrophic lateral sclerosis (ALS) : study protocol for a qualitative longitudinal study with persons with ALS and their family carers
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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