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Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|June 21, 2002
Oral manifestations of patients with Marfan syndrome: a case-control studyP J A De Coster, L C M Martens, A De PaepeJournal 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.Cell Death and Differentiation|September 26, 2009
Escape from p53-mediated tumor surveillance in neuroblastoma: switching off the p14(ARF)-MDM2-p53 axisT Van Maerken, J Vandesompele, A Rihani, et al.Archives of Internal Medicine|December 1, 2001
Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndromeB Loeys, L Nuytinck, I Delvaux, et al.Journal of Medical Genetics|May 12, 2000
Glycine to tryptophan substitution in type I collagen in a patient with OI type III: a unique collagen mutationL Nuytinck, T Tükel, H Kayserili, et al.American Journal of Human Genetics|March 1, 1997
Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and IIA De Paepe, L Nuytinck, I Hausser, et al.Cytotechnology|January 1, 1993
Cell-matrix interactions in cultured dermal fibroblasts from patients with an inherited connective-tissue disorderM Baccarani Contri, R Tiozzo, M A Croce, et al.American Journal of Medical Genetics|May 7, 2002
Homozygous Gly530Ser substitution in COL5A1 causes mild classical Ehlers-Danlos syndromeC Giunta, L Nuytinck, M Raghunath, et al.The International Journal of Behavioral Nutrition and Physical Activity|July 8, 2021
Effectiveness of the mHealth intervention 'MyDayPlan' to increase physical activity: an aggregated single case approachL Degroote, A De Paepe, I De Bourdeaudhuij, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|November 1, 1989
Obstetrical problems in patients with Ehlers-Danlos syndrome type IV; a case reportA De Paepe, B Thaler, M Van Gijsegem, et al.Pageof 15