prof. dr. Fransiska Malfait
- ORCID iD
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0000-0002-5010-0304
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Classic Ehlers-Danlos syndrome
(2024) GeneReviews®. -
- Journal Article
- A1
- open access
Reduced capsaicin-induced mechanical allodynia and neuronal responses in the dorsal root ganglion in the presence of protein tyrosine phosphatase non-receptor type 6 overexpression
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- Conference Paper
- C3
- open access
When the phenotype is more severe than expected : coexistence of X-linked and dominant ichthyosis in an African patient
(2024) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 32(Supplement 1). p.402-402 -
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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The Ehlers-Danlos syndromes
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- Journal Article
- A1
- open access
Sensory profiling in classical Ehlers-Danlos syndrome : a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation
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Syntaxin-18 defects in human and zebrafish cause traffic jams and unravel key roles in early bone development
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.394-394 -
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