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Affichage: 1 - 25 sur 361 résultats.

Pages

    • Article de périodique
    Unravelling the molecular genetics of osteoarthrosis
    Vikkula, Miikka[UCL] Olsen, Bjorn R. (1996) Annals of Medicine — Vol. 28, no.4, p. 301-304 (1996)
    • Chapitre
    Angiopoietins, TIEs, Ephrins, VEGFs and VEGFRs
    Vikkula, Miikka[UCL] Karkkainen, Marika J. Alitalo, Kari (2004) Inborn errors of development: the molecular basis of clinical disorders on morphogenesis — [ISBN : 0-19-514502-X]
    • Article de périodique
    Inheritance Patterns of Infantile Hemangioma.
    Castrén, Eeva Salminen, Päivi Vikkula, Miikka[UCL] Pitkäranta, Anne Klockars, Tuomas (2016) Pediatrics — Vol. 138, no. 5, p. e20161623 [1-9] (2016)
    • Article de périodique
    Type II collagen mutations in rare and common cartilage diseases.
    Vikkula, Miikka[UCL] Metsäranta, M Ala-Kokko, L (1994) Annals of medicine — Vol. 26, no.2, p. 107-14 (1994)
    • Article de périodique
    Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?
    Lannoy, Nathalie[UCL] Lambert, Catherine[UCL] Vikkula, Miikka[UCL] Hermans, Cédric[UCL] (2015) Thrombosis Research : vascular obstruction, hemorrhage and hemostasis — Vol. 135, no. 6, p. 1057-1063 (2015)
    • Article de périodique
    Age-related heterogeneity of Burkitt lymphoma: response to Mbulaiteye and Anderson.
    Poirel, Hélène[UCL] Vikkula, Miikka[UCL] (2018) British Journal of Haematology — Vol. 180, no. 1, p. 155-156 (2018)
    • Article de périodique
    Multiallelic polymorphism of the cartilage collagen gene: no association with osteoarthrosis.
    Vikkula, Miikka[UCL] Nissilä, M Hirvensalo, E Nuotio, P Palotie, A Aho, K Peltonen, L (1993) Annals of the rheumatic diseases — Vol. 52, no.10, p. 762-4 (1993)
    • Chapitre
    Les biomarqueurs de risque cardiovasculaire à l'heure de la génomique
    Persu, Alexandre[UCL] Vikkula, Miikka[UCL] (2010) Athérosclérose Athérothrombose — [ISBN : 978-9-0810-5422-5]
    • Article de périodique
    Heredity of port-wine stains: investigation of families without a RASA1 mutation.
    Troilius Rubin, Agneta Lauritzen, Edgar Ljunggren, Bo Revencu, Nicole[UCL] Vikkula, Miikka[UCL] Svensson, Åke (2015) Journal of Cosmetic and Laser Therapy — Vol. 17, no.4, p. 204-208 (2015)
    • Communication
    Towards a Venous Malformation Mouse Model
    Uebelhoer, Mélanie[UCL] Limaye, Nisha[UCL] Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] (2010) 18th Workshop on Vascular Anomalies — Brussels, Belgium
    • Article de périodique
    Antenatal presentation of hereditary lymphedema type I.
    Boudon, E. Levy, Y. Abossolo, T. Cartault, François Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] Kieffer-Traversier, M. Ramful, D. Alessandri, J. L. (2015) European Journal of Medical Genetics — Vol. 58, no.6-7, p. 329-331 (2015)

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