Fransiska Malfait

9PUBLICATIONS
41CO-AUTHORS
Cardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Major global burdens of diseaseInfant and child healthMedical genetics (excl. cancer genetics)
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Publications (9)

|Oct 06, 2022
Publisher Correction: The impact of COVID-19 on rare and complex connective tissue diseases: the experience of ERN ReCONNET.

Rosaria Talarico, Silvia Aguilera, Tobias Alexander

|Aug 22, 2022
Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos syndromes.

Delfien Syx, Sarah Delbaere, Catherine Bui

|Nov 19, 2021
Pain in the Ehlers-Danlos syndromes: Mechanisms, models, and challenges.

Fransiska Malfait, Marlies Colman, Robin Vroman

|Jul 17, 2021
Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen.

Tibbe Dhooge, Delfien Syx, Trinh Hermanns-Lê

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