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Displaying 12 results.
    • 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
    • Journal article
    Surgical Management of Infantile Hemangioma Using the Purse-String Technique: Impact on the Scar
    Coulie, Julien Coyette, Maude Boon, Laurence M.[UCL] (2015) Plastic and Reconstructive Surgery — Vol. 136, no.4 Suppl, p. 156 (2015)
    • Journal article
    Somatic Activating PIK3CA Mutations Cause Venous Malformation
    Limaye, Nisha[UCL] Kangas, Jaakko Mendola, Antonella[UCL] Godfraind, Catherine Schlögel, Matthieu[UCL] Helaers, Raphaël[UCL] Eklund, Lauri Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2015) American Journal of Human Genetics — Vol. 97, no. 6, p. 914-921 (2015)
    • Journal article
    Common and specific effects of TIE2 mutations causing venous malformations.
    Nätynki, Marjut Kangas, Jaakko Miinalainen, Ilkka Sormunen, Raija Pietilä, Riikka Soblet, Julie[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] Limaye, Nisha[UCL] Eklund, Lauri (2015) Human Molecular Genetics — Vol. 24, no. 22, p. 6374-6389 (2015)
    • BookChapter
    Blue bleb rubber nevus syndrome
    Ballieux, Fanny[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2015) Handbook of Clinical Neurology : Neurocutaneous Syndromes — [ISBN : 978-0-444-62702-5]
    • 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) —
    • Journal article
    Blue bleb rubber nevus syndrome.
    Ballieux, Fanny[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2015) Handbook of Clinical Neurology : revised series — Vol. 132, no.x, p. 223-30 (2015)
    • Journal article
    Multidisciplinary management of giant genital tract venous malformations during pregnancy: case report and review of the literature
    Hubinont, Corinne[UCL] Roelants, Fabienne[UCL] Boon, Laurence M.[UCL] Minlangu , Ana Bila[UCL] Hermans, Cédric[UCL] Debiève, Frédéric[UCL] (2015) Case Reports in Perinatal Medicine — Vol. 4, no.2, p. 101–104 (2015)
    • Journal article
    Treatment of infantile haemangiomas: recommendations of a European expert group.
    Hoeger, Peter H Harper, John I Baselga, Eulalia Bonnet, Damien Boon, Laurence M.[UCL] Atti, Marta Ciofi Degli El Hachem, Maya Oranje, Arnold P Rubin, Agneta Troilius Weibel, Lisa Léauté-Labrèze, Christine (2015) European Journal of Pediatrics — Vol. 174, no. 7, p. 855-865 (2015)
    • Journal article
    Rapamycin improves TIE2-mutated venous malformation in murine model and human subjects
    Boscolo, Elisa Limaye, Nisha[UCL] Huang, Lan Kang, Kyu-Tae Soblet, Julie[UCL] Uebelhoer, Mélanie[UCL] Mendola, Antonella[UCL] Natynki, Marjut Seront, Emmanuel[UCL] Dupont, Sophie[UCL] Hammer, Jennifer[UCL] Legrand, Catherine[UCL] Brugnara, Carlo Eklund, Lauri Vikkula, Miikka[UCL] Bischoff, Joyce Boon, Laurence M.[UCL] (2015) Journal of Clinical Investigation — Vol. 125, no. 9, p. 3491-3504 (2015)
    • BookChapter
    Genetic causes of lymphedema
    Schlögel, Matthieu[UCL] Brouillard, Pascal[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2015) Lymphedema: Presentation, Diagnosis and Treatment — [ISBN : 978-3-319-14493-1]
    • Journal article
    No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
    Schlögel, Matthieu[UCL] Mendola, Antonella[UCL] Fastre, Elodie[UCL] Vasudevan, Pradeep Devriendt, Koen de Ravel, Thomy Jl Van Esch, Hilde Casteels, Ingele Arroyo Carrera, Ignacio Cristofoli, Francesca Fieggen, Karen Jones, Katheryn Lipson, Mark Balikova, Irina Singer, Ami Soller, Maria Mercedes Villanueva, María Revencu, Nicole[UCL] Boon, Laurence M.[UCL] Brouillard, Pascal[UCL] Vikkula, Miikka[UCL] (2015) Orphanet Journal of Rare Diseases — Vol. 10, no. 1, p. 52 (2015)