Trinh Hermanns‐Lê

Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen

Lieve Nuytinck, M. Freund, Lieven Lagae et al. · The American Journal of Human Genetics · 2000 · 176 citations · Full text

Mendelian Disorder, Autoimmune Disease, Genetic Disorder +5

Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood

Fransiska Malfait, Sofie Symoens, Julie De Backer et al. · Human Mutation · 2007 · 160 citations · Full text

Collagen Fibrils, Vascular Disease, Genetics +18

Evidence for a relationship between Ehlers–Danlos type VII C in humans and bovine dermatosparaxis

B Nusgens, Ch. Verellen-Dumoulin, Trinh Hermanns‐Lê et al. · Nature Genetics · 1992 · 131 citations · Full text

Autoimmune Disease, Allergy, Animal Science +12

Dermal Ultrastructure in Low Beighton Score Members of 17 Families with Hypermobile-Type Ehlers-Danlos Syndrome

Trinh Hermanns‐Lê, Marie‐Annick Reginster, C Piérard-Franchimont et al. · Journal of Biomedicine and Biotechnology · 2012 · 120 citations · Full text

Rheumatology, Transmission Electron Microscopy, Genetic Disorder +14

Musculocontractural Ehlers-Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene

Fransiska Malfait, Delfien Syx, Philip Vlummens et al. · Human Mutation · 2010 · 119 citations · Full text

Eds Vib Phenotype, Genetics, Thumb Clubfoot Syndrome +19