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F Malfait

Showing results (1-10 of 14) with videos related to

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Clinical Genetics|February 23, 2012
The Ehlers-Danlos syndrome, a disorder with many facesA De Paepe, F Malfait
Rheumatology (Oxford, England)|January 19, 2006
The genetic basis of the joint hypermobility syndromesF Malfait, A J Hakim, A De Paepe, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 2, 2010
Vascular haemostasisN S Key, A DE Paepe, F Malfait, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|September 13, 2003
Unusual oral findings in dermatosparaxis (Ehlers-Danlos syndrome type VIIC)P J De Coster, F Malfait, L C Martens, et al.
Journal of Medical Genetics|July 4, 2006
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 problemsF Malfait, S Symoens, P Coucke, et al.
Journal of Medical Genetics|July 6, 2004
Met>Val substitution in a highly conserved region of the pro-alpha1(I) collagen C-propeptide domain causes alternative splicing and a mild EDS/OI phenotypeS Symoens, L Nuytinck, E Legius, et al.
Molecular Genetics and Metabolism|December 14, 2004
Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 geneL C Walker, A S Teebi, J C Marini, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 25, 2019
Higher fracture prevalence and smaller bone size in patients with hEDS/HSD-a prospective cohort studyT Banica, M Coussens, C Verroken, et al.
Journal of Medical Genetics|December 18, 2008
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylationA Willaert, F Malfait, S Symoens, et al.
American Journal of Medical Genetics. Part A|February 4, 2012
Superior mesenteric artery aneurysm in a 9-year-old boy with classical Ehlers-Danlos syndromeK de Leeuw, J F Goorhuis, I F J Tielliu, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Clinical Genetics|February 23, 2012
The Ehlers-Danlos syndrome, a disorder with many facesA De Paepe, F Malfait
Rheumatology (Oxford, England)|January 19, 2006
The genetic basis of the joint hypermobility syndromesF Malfait, A J Hakim, A De Paepe, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 2, 2010
Vascular haemostasisN S Key, A DE Paepe, F Malfait, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|September 13, 2003
Unusual oral findings in dermatosparaxis (Ehlers-Danlos syndrome type VIIC)P J De Coster, F Malfait, L C Martens, et al.
Journal of Medical Genetics|July 4, 2006
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 problemsF Malfait, S Symoens, P Coucke, et al.
Journal of Medical Genetics|July 6, 2004
Met>Val substitution in a highly conserved region of the pro-alpha1(I) collagen C-propeptide domain causes alternative splicing and a mild EDS/OI phenotypeS Symoens, L Nuytinck, E Legius, et al.
Molecular Genetics and Metabolism|December 14, 2004
Decreased expression of lysyl hydroxylase 2 (LH2) in skin fibroblasts from three Ehlers-Danlos patients does not result from mutations in either the coding or proximal promoter region of the LH2 geneL C Walker, A S Teebi, J C Marini, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|December 25, 2019
Higher fracture prevalence and smaller bone size in patients with hEDS/HSD-a prospective cohort studyT Banica, M Coussens, C Verroken, et al.
Journal of Medical Genetics|December 18, 2008
Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylationA Willaert, F Malfait, S Symoens, et al.
American Journal of Medical Genetics. Part A|February 4, 2012
Superior mesenteric artery aneurysm in a 9-year-old boy with classical Ehlers-Danlos syndromeK de Leeuw, J F Goorhuis, I F J Tielliu, et al.
Pageof 2