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Displaying 23 results.
    • Speech
    Lack of glomulin, a specific marker of vascular smooth muscle cell differentiation, causes glomuvenous malformations
    Brouillard, Pascal[UCL] Boon, Laurence M.[UCL] McIntyre, B. A. S. Vassilev, V. S. Mulliken, J. B. Vikkula, Miikka[UCL] (2006) 14th International Vascular Biology Meeting — Noordwijkerhout (Netherlands)
    • Speech
    Noninvoluting congenital hemangioma: A rare cutaneous vascular anomaly
    Enjolras, Odile Mulliken, John B. Boon, Laurence M.[UCL] Wassef, Michel Kozakewich, Harry P. W. Burrows, Patricia E. (2001) Biennial Meeting of the International-Society-for-the-Study-of-Vascular-Anomalies — BERLIN (Germany)
    • Speech
    Glomuvenous malformation ("glomangioma") is a distinct clinicopathologic and genetic entity
    Boon, Laurence M.[UCL] Mulliken, J Enjolras, O Vikkula, Miikka[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
    • Speech
    Inherited glomuvenous malformations are caused by the combination of a germline and a somatic "second hit" mutation in the glomulin gene
    Brouillard, Pascal[UCL] Boon, Laurence M.[UCL] Ghassibé, Michella[UCL] Enjolras, O Mulliken, J Vikkula, Miikka[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
    • Speech
    Inherited capillary malformation is associated with a high flow vascular malformation
    Boon, Laurence M.[UCL] Mulliken, J Bataille, A Lengelé, Benoît[UCL] Vittu, G Vanwijck, Romain Vikkula, Miikka[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
    • Speech
    Inherited capillary malformation is associated with a high flow vascular malformation.
    Boon, Laurence M.[UCL] Vanwijck, Romain[UCL] Mulliken, JB Bataille, AC Vittu, G Vikkula, Miikka[UCL] (2002) 52nd Annual Meeting of the American-Society-of-Human-Genetics — BALTIMORE (Maryland)
    • Speech
    Familial capillary malformation maps to chromosome 5q
    Eerola, I Boon, Laurence M.[UCL] Watanabe, S Grynberg, H Mulliken, J Vikkula, Miikka[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
    • Speech
    Identification of novel glomulin gene mutations responsible for inherited glomuvenous malformations (glomangiomas).
    Brouillard, Pascal[UCL] Ghassibé, Michella[UCL] Boon, Laurence M.[UCL] Penington, A Enjolras, O Mulliken, JB Vikkula, Miikka[UCL] (2002) 52nd Annual Meeting of the American-Society-of-Human-Genetics — BALTIMORE (Maryland)
    • Speech
    Identification of the gene responsible for familial capillary malformation.
    Vikkula, Miikka[UCL] Eerola, I Boon, Laurence M.[UCL] Watanabe, S Mulliken, JB (2002) 52nd Annual Meeting of the American-Society-of-Human-Genetics — BALTIMORE (Maryland)
    • Speech
    Somatic second hit-hypothesis is true for glomuvenous malformations.
    Brouillard, Pascal[UCL] Boon, Laurence M.[UCL] Enjolras, O Ghassibé, Michella[UCL] Mulliken, JB Vikkula, Miikka[UCL] (2001) —
    • Speech
    Truncating mutations in the glomulin gene cause glomuvenous malformations.
    Vikkula, Miikka[UCL] Brouillard, Pascal[UCL] Mulliken, JB Enjolras, O Warman, ML Tan, OT Olsen, BR Boon, Laurence M.[UCL] (2001) —
    • Speech
    Acquired Uniparental isodisomy as a common somatic 2nd-hit explains multifocality of glomuvenous malformation
    Amyere, Mustapha[UCL] Aerts, Virginie[UCL] Duhoux, François[UCL] Brouillard, Pascal[UCL] Wassef, Michel Enjolras, Odile Mulliken, John B Poirel, Hélène[UCL] Devuyst, Olivier[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2010) 10th Annual Meeting of the Belgian Society of Human Genetics — Ghent
    • Speech
    Capillary-venous malformation in the labia majora in a 12-year-old girl
    Kempinaire, A Boon, Laurence M.[UCL] DeRaeve, L Roseeuw, D. DeRaeve, H (1997) Meeting of the Belgian-Royal-Society-for-Dermatology-and-Venereology — BRUSSELS (Belgium)
    • Speech
    Acquired uniparental isodisomy as a common somatic 2nd-hit explains multifocality of glomuvenous malformations
    Vikkula, Miikka[UCL] Aerts, Virginie[UCL] Duhoux, François[UCL] Brouillard, Pascal[UCL] Wassef, Michel Enjolras, Odile Mulliken, John B Poirel, Hélène[UCL] Devuyst, Olivier[UCL] Boon, Laurence M.[UCL] Amyere, Mustapha[UCL] (2010) European Human Genetics Conference — Goeteborg, Suède
    • Speech
    Surgical treatment of knee vascular malformations
    Docquier, Pierre-Louis[UCL] Pireau, Nathalie[UCL] Poilvache, Pascal[UCL] Boon, Laurence M.[UCL] (2010) 18th International Society for Study of Vascular Anomalies (ISSVA) Congress — (Belgium) Bruxelles
    • Speech
    Rapamycin as Novel Treatment for Refractory-to-Standard-Care Slow-Flow Vascular Malformations.
    Boon, Laurence M.[UCL] Hammer, Jennifer[UCL] Seront, Emmanuel[UCL] Dupont, Sophie[UCL] Hammer, Frank[UCL] Clapuyt, Philippe[UCL] Vikkula, Miikka[UCL] (2015) Plastic Surgery 2015: Plastic Surgery The Meeting 2015 — (United States) Boston, MA
    • Speech
    Has Propranolol Eradicated the Need for Surgery in the Management of Infantile Hemangioma?
    Coulie, Julien[UCL] Coyette, Maude[UCL] Moniotte, Stéphane[UCL] Bataille, Anne-Christine[UCL] Boon, Laurence M.[UCL] (2015) —
    • Speech
    Management of CLOVES syndrome
    Baillieux, Fanny Modaressi, Ali Docquier, Pierre-Louis[UCL] Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2010) 18th International Society for Study of Vascular Anomalies (ISSVA) Congress — (Belgium) Bruxelles
    • Speech
    Somatic TIE2 mutations in sporadic venous malformations
    Uebelhoer, Mélanie[UCL] Soblet, Julie[UCL] Wouters, Vinciane[UCL] Mulliken, John B. Eklund, Lauri Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2010) International Vascular Biology Meeting — Los Angeles, USA
    • Speech
    Various Activating TIE2 Tyrosine Kinase Domain Mutations, Including the Recurrent R849W Substitution, Cause Cutaneomucosal Venous Malformation (VMCM) in a Paradominant Fashion.
    Uebelhoer, Mélanie[UCL] Limaye, Nisha[UCL] Wouters, Vinciane[UCL] Irrthum, Alexandre[UCL] Boon, Laurence M.[UCL] (2008) 8t Annual Meeting of the Belgian Society of Human Genetics — Leuven, Belgium
    • Speech
    Sporadic venous malformation is caused by somatic mutations in TIE2
    Uebelhoer, Mélanie[UCL] Wouters, Vinciane[UCL] Boon, Laurence M.[UCL] Mulliken, John B. Vikkula, Miikka[UCL] (2008) European Society of Human Genetics — Barcelona, Spain
    • Speech
    Various activating TIE2 tyrosine kinase domain mutations, including the recurrent R849W substitution, cause cutaneomucosal venous malformation (VMCM) in a paradominant fashion
    Limaye, Nisha[UCL] Wouters, Vinciane[UCL] Uebelhoer, Mélanie[UCL] Irrthum, Alexandre[UCL] Boon, Laurence M.[UCL] (2007) 57th Annual Meeting of the American Society of Human Genetics — San Diego, USA
    • Speech
    Prise en charge des hémangiomes infantiles
    Bataille, Anne-Christine[UCL] Boon, Laurence M.[UCL] Moniotte, Stéphane[UCL] (2014) 69th meeting of the 'Groupement Belge des Pédaitres de Langue Française' — (Belgium) charleroi