Хайлтын үр дүнгүүд - Trinh Hermanns‐Lê

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  1. 1
    Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen

    Classical Ehlers-Danlos Syndrome Caused by a Mutation in Type I Collagen -н Lieve Nuytinck, M. Freund, Lieven Lagae, Gérald Pierard, Trinh Hermanns‐Lê, Anne De Paepe

    Хэвлэсэн 2000
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    Artigo
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  2. 2
    Dermal Ultrastructure in Low Beighton Score Members of 17 Families with Hypermobile-Type Ehlers-Danlos Syndrome

    Dermal Ultrastructure in Low Beighton Score Members of 17 Families with Hypermobile-Type Ehlers-Danlos Syndrome -н Trinh Hermanns‐Lê, Marie‐Annick Reginster, C Piérard-Franchimont, Philippe Delvenne, Gérald Pierard, Daniel Manicourt

    Хэвлэсэн 2012
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    Artigo
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  3. 3
    Evidence for a relationship between Ehlers–Danlos type VII C in humans and bovine dermatosparaxis

    Evidence for a relationship between Ehlers–Danlos type VII C in humans and bovine dermatosparaxis -н B Nusgens, Ch. Verellen-Dumoulin, Trinh Hermanns‐Lê, Anne De Paepe, Lieve Nuytinck, Gérald Pierard, Ch.M. Lapière

    Хэвлэсэн 1992
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    Artigo
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  4. 4
    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

    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-... -н Fransiska Malfait, Delfien Syx, Philip Vlummens, Sofie Symoens, Sheela Nampoothiri, Trinh Hermanns‐Lê, Lut Van Laer, Anne De Paepe

    Хэвлэсэн 2010
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    Artigo
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  5. 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

    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 -н Fransiska Malfait, Sofie Symoens, Julie De Backer, Trinh Hermanns‐Lê, Natzi Sakalihasan, Charles M. Lapière, Paul Coucke, Anne De Paepe

    Хэвлэсэн 2007
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    Artigo
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  6. 6
    Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic <i>BMP1</i> Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta

    Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic <i>BMP1</i> Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta -н Delfien Syx, Brecht Guillemyn, Sofie Symoens, Ana Berta Sousa, Ana Medeira, Margo Whiteford, Trinh Hermanns‐Lê, Paul Coucke, Anne De Paepe, Fransiska Malfait

    Хэвлэсэн 2015
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    Artigo
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