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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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Late-onset Pompe disease (LOPD) in Belgium : clinical characteristics and outcome measures
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Database crossing allows better understanding of neuromuscular disorders epidemiology: the Belgian example
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A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome