prof. dr. Fransiska Malfait
- ORCID iD
- 0000-0002-5010-0304
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- Journal Article
- open access
Impaired muscle parameters in adults with mild to severe types of osteogenesis imperfecta: a cross-sectional study
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- Journal Article
- A1
- open access
Flemish network on rare connective tissue diseases (CTD) : patient pathways in systemic sclerosis : first steps taken
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- Journal Article
- open access
NRF2 Shortage in Human Skin Fibroblasts Dysregulates Matrisome Gene Expression and Affects Collagen Fibrillogenesis
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- Journal Article
- A1
- open access
Analysis of matrisome expression patterns in murine and human dorsal root ganglia
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Syntaxin 18 defects in human and zebrafish unravel key roles in early cartilage and bone development
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- Journal Article
- A1
- open access
Somatic symptoms, pain, catastrophizing and the association with disability among children with heritable connective tissue disorders
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Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation
(2023) -
- Journal Article
- A1
- open access
A tapt1 knock-out zebrafish line with aberrant lens development and impaired vision models human early-onset cataract
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Bone parameters in hypermobile Ehlers-Danlos syndrome and hypermobility spectrum disorder : a comparative cross-sectional study
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Home-based exercise therapy for treating shoulder instability in patients with hypermobile Ehlers-Danlos syndrome/hypermobility spectrum disorders : a randomized trial