Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin
Gistelinck, C, Gioia, R, Gagliardi, A, Tonelli, F, Marchese, L, Bianchi, L, Landi, C, Bini, L, Huysseune, A, Witten, P E, Staes, A, Gevaert, K, De Rocker, N, Menten, B, Malfait, F, Leikin, S, Carra, S, Tenni, R, Rossi, A, De Paepe, A, Coucke, P, Willaert, A, Forlino, A
Published in Scientific reports (15.02.2016)
Published in Scientific reports (15.02.2016)
Get full text
Journal Article
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type
Malfait, Fransiska, Wenstrup, Richard J., De Paepe, Anne
Published in Genetics in medicine (01.10.2010)
Published in Genetics in medicine (01.10.2010)
Get full text
Journal Article
Higher fracture prevalence and smaller bone size in patients with hEDS/HSD—a prospective cohort study
Banica, T., Coussens, M., Verroken, C., Calders, P., De Wandele, I., Malfait, F., Zmierczak, H.-G., Goemaere, S., Lapauw, B., Rombaut, L.
Published in Osteoporosis international (01.05.2020)
Published in Osteoporosis international (01.05.2020)
Get full text
Journal Article
The genetic basis of the joint hypermobility syndromes
Malfait, F., Hakim, A. J., De Paepe, A., Grahame, R.
Published in Rheumatology (Oxford, England) (01.05.2006)
Published in Rheumatology (Oxford, England) (01.05.2006)
Get full text
Journal Article
Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
Kelley, B. P, Malfait, F, Bonafe, L, Baldridge, D, Homan, E, Symoens, S, Willaert, A, Elcioglu, N, Van Maldergem, Lionel, Verellen-Dumoulin, C, Gillerot, Y, Napierala, D, Krakow, D, Beighton, P, Superti-Furga, A, De Paepe, Alexandra, Lee, B
Published in Journal of bone and mineral research (01.03.2011)
Published in Journal of bone and mineral research (01.03.2011)
Get full text
Journal Article
Web Resource
Total absence of the alpha2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems
Malfait, F, Symoens, S, Coucke, P, Nunes, L, De Almeida, S, De Paepe, A
Published in Journal of medical genetics (01.07.2006)
Published in Journal of medical genetics (01.07.2006)
Get full text
Journal Article
Total absence of the alpha 2(I) chain of collagen type I causes a rare form of Ehlers-Danlos syndrome with hypermobility and propensity to cardiac valvular problems
Malfait, F, Symoens, S, Coucke, P, Nunes, L, De Almeida, S, De Paepe, A
Published in Journal of medical genetics (01.07.2006)
Published in Journal of medical genetics (01.07.2006)
Get full text
Journal Article
Flemish network on rare connective tissue diseases (CTD): patient pathways in systemic sclerosis. First steps taken
Piette, Y, Van den Bossche, F, Aerts, J, Aerts, N, Ajeganova, S, Badot, V, Berghen, N, Blockmans, D, Brusselle, G, Caeyers, N, De Decker, M, De Haes, P, De Cock, C, De Keyser, F, De Langhe, E, Delcroix, M, De Nutte, H, De Pauw, M, Depicker, A, De Sutter, A, De Sutter, J, Du Four, T, Frank, C, Goubau, J, Guiot, J, Gutermuth, J, Heeman, L, Houssiau, F, Hennes, I, Lenaerts, J, Lintermans, A, Loeys, B, Luyten, H, Maeyaert, B, Malfait, F, Moeyersoons, A, Mostmans, Y, Nijs, J, Poppe, B, Polfliet, K, Ruttens, D, Sabato, V, Schoeters, E, Slabbynck, H, Stuer, A, Tamirou, F, Thevissen, Kristof, Van Kersschaever, G, Vanneuville, B, Van Offel, J, Vanthuyne, M, Van Wabeke, J, Verbist, C, Vos, I, Westhovens, R, Wuyts, W, Yserbyt, J, Smith, V
Published in Acta clinica belgica (English ed. Online) (01.02.2024)
Published in Acta clinica belgica (English ed. Online) (01.02.2024)
Get more information
Journal Article
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation
Willaert, A, Malfait, F, Symoens, S, Gevaert, K, Kayserili, H, Megarbane, A, Mortier, G, Leroy, J G, Coucke, P J, De Paepe, A
Published in Journal of medical genetics (01.04.2009)
Published in Journal of medical genetics (01.04.2009)
Get full text
Journal Article
Ehlers-Danlos arthrochalasia type (VIIA-B) - expanding the phenotype: from prenatal life through adulthood
Klaassens, M, Reinstein, E, Hilhorst-Hofstee, Y, Schrander, JJP, Malfait, F, Staal, H, ten Have, LC, Blaauw, J, Roggeveen, HCJ, Krakow, D, De Paepe, A, van Steensel, MAM, Pals, G, Graham, JM, Schrander-Stumpel, CTRM
Published in Clinical genetics (01.08.2012)
Published in Clinical genetics (01.08.2012)
Get full text
Journal Article
Endogenous pain modulation in the Ehlers–Danlos syndrome, hypermobility type
De Wandele, I, Hermans, L, Rombaut, L, Meeus, M, Brusselmans, G, Malfait, F, De Paepe, A, Calders, P
Published in Osteoarthritis and cartilage (01.04.2014)
Published in Osteoarthritis and cartilage (01.04.2014)
Get full text
Journal Article
Chronic pain in patients with the hypermobility type of Ehlers–Danlos syndrome: evidence for generalized hyperalgesia
Rombaut, L, Scheper, M, De Wandele, I, De Vries, J, Meeus, M, Malfait, F, Engelbert, R, Calders, P
Published in Osteoarthritis and cartilage (01.04.2014)
Published in Osteoarthritis and cartilage (01.04.2014)
Get full text
Journal Article
Superior mesenteric artery aneurysm in a 9‐year‐old boy with classical Ehlers–Danlos syndrome
de Leeuw, K., Goorhuis, J.F., Tielliu, I.F.J., Symoens, S., Malfait, F., de Paepe, A., van Tintelen, J.P., Hulscher, J.B.F.
Published in American journal of medical genetics. Part A (01.03.2012)
Published in American journal of medical genetics. Part A (01.03.2012)
Get full text
Journal Article
Novel Types of Mutation Responsible for the Dermatosparactic Type of Ehlers–Danlos Syndrome (Type VIIC) and Common Polymorphisms in the ADAMTS2 Gene
Colige, Alain, Nuytinck, Lieve, Hausser, Ingrid, van Essen, Anthonie J., Thiry, Marc, Herens, Christian, Adès, Lesley C., Malfait, Fransiska, Paepe, Anne De, Franck, Peter, Wolff, Gerhard, Oosterwijk, Jan C., Sillevis Smitt, J.H., Lapière, Charles M., Nusgens, Betty V.
Published in Journal of investigative dermatology (01.10.2004)
Published in Journal of investigative dermatology (01.10.2004)
Get full text
Journal Article
Web Resource
500 HEALTH STATUS AND IMPACT OF PAIN: A COMPARATIVE STUDY BETWEEN FEMALE PATIENTS WITH THE EHLERS-DANLOS SYNDROME FIBROMYALGIA AND RHEUMATOID ARTHRITIS
Rombaut, L, Malfait, F, Rimbaut, S, Vander Cruyssen, B, De Paepe, A, Calders, P
Published in Osteoarthritis and cartilage (2010)
Published in Osteoarthritis and cartilage (2010)
Get full text
Journal Article
Vascular haemostasis
KEY, N. S., DE PAEPE, A., MALFAIT, F., SHOVLIN, C. L.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2010)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2010)
Get full text
Journal Article
The natural history, including orofacial features of three patients with Ehlers-Danlos syndrome, dermatosparaxis type (EDS type VIIC)
Malfait, Fransiska, De Coster, Peter, Hausser, Ingrid, van Essen, Anthonie J., Franck, Peter, Colige, Alain, Nusgens, Betty, Martens, Luc, De Paepe, Anne
Published in American journal of medical genetics. Part A (15.11.2004)
Published in American journal of medical genetics. Part A (15.11.2004)
Get full text
Journal Article
Web Resource