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Displaying 13 results.
    • Journal article
    Sporadic In Utero Generalized Edema Caused by Mutations in the Lymphangiogenic Genes VEGFR3 and FOXC2.
    Ghalamkarpour, Arash Debauche, Christian[UCL] Haan, Eric Van Regemorter, Nicole Sznajer, Yves Thomas, Dominique Revencu, Nicole Gillerot, Yves Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) The Journal of pediatrics — Vol. 155, no. 1, p. 90-3 (2009)
    • Journal article
    Rare presentation of familial paraganglioma without evidence of mutation in the SDH, RET and VHL genes: towards further genetic heterogeneity.
    Persu, Alexandre[UCL] Amyere, Mustapha[UCL] Gutierrez-Roelens, Ilse[UCL] Rustin, Pierre Sempoux, Christine[UCL] Lecouvet, Frédéric[UCL] Van Beers, Bernard[UCL] Horsmans, Yves[UCL] De Plaen, Jean-François[UCL] Hamoir, Marc[UCL] Vikkula, Miikka[UCL] (2009) Journal of Hypertension — Vol. 27, no. 1, p. 76-82 (2009)
    • Journal article
    Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome
    Ferreira de Lima, Renata Hoper, Sarah Ghassibé, Michella[UCL] Cooper, Margaret Rorick, Nicholas Kondo, Shinji Katz, Lori Marazita, Mary Compton, John Bale, Sherri Hehr, Ute Dixon, Michael Daack-Hirsch, Sandra Boute, Odile Bayet, Bénédicte[UCL] Revencu, Nicole[UCL] Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] Richieri-Costa, Antônio Moretti-Ferreira, Danilo Murray, Jeffrey Schutte, Brian (2009) Genetics in Medicine — Vol. 11, no. 4, p. 241-247 (2009)
    • Journal article
    From germline towards somatic mutations in the pathophysiology of vascular anomalies.
    Limaye, Nisha[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) Human molecular genetics — Vol. 18, no. R1, p. R65-74 (2009)
    • Journal article
    Recessive primary congenital lymphoedema caused by a VEGFR3 mutation
    Ghalamkarpour, Arrask[UCL] Holnthoner, Wolfgang Saharinen, Pipsa Boon, Laurence M.[UCL] Mulliken, John B. Alitalo, Kari Vikkula, Miikka[UCL] (2009) Journal of Medical Genetics — Vol. 46, no. 6, p. 399-404 (2009)
    • Journal article
    From Blue Jeans to Blue Genes.
    Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) Journal of Craniofacial Surgery — Vol. 20 Suppl 1, p. 703-7066 (2009)
    • Journal article
    Elevated D-dimer Level in the Differential Diagnosis of Venous Malformations
    Dompmartin, Anne Hermans, Cédric[UCL] Clapuyt, Philippe[UCL] Boon, Laurence M.[UCL] Ballieux, Fanny[UCL] Thibon, Pascal Lequerrec, Agnes Barrellier, Marie-Therese Hammer, Frank[UCL] Labbe, Daniel Vikkula, Miikka[UCL] (2009) Archives of Dermatology — Vol. 145, no. 11, p. 1239-44 (2009)
    • Journal article
    Molecular Genetics of Hereditary Vascular Malformations
    Aerts, Virginie[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) Encyclopedia of Life Sciences — Vol. xxx, no.xx, p. 1-8 (2009)
    • Journal article
    Trisomy 19 ependymoma
    Godfraind, Catherine[UCL] Vikkula, Miikka[UCL] (2009) Atlas of Genetics and Cytogenetics in Oncology and Haematology — Vol. 13, no.1, p. 90-92 (2009)
    • BookChapter
    Genetic aspects of vascular malformations
    Limaye, Nisha[UCL] Vikkula, Miikka[UCL] (2009) Hemangiomas and Vascular Malformations. An Atlas of Diagnosis and Treatment — [ISBN : 978-88-470-0568-6.]
    • Journal article
    Somatic mutations in the angiopoietin-receptor TIE2 can cause both solitary and multiple sporadic venous malformations
    Limaye, Nisha[UCL] Wouters, Vinciane[UCL] Uebelhoer, Mélanie[UCL] Tuominen, Marjut Wirkkala, Riikka Mulliken, John B. Eklund, Lauri Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2009) Nature Genetics — Vol. 41, no. 1, p. 118-124 (2009)
    • Journal article
    Nervous system: trisomy 19 ependymoma
    Godfraind, Catherine[UCL] Vikkula, Miikka[UCL] (2009) Atlas of genetics and cytogenetics in oncology and haematology — Vol. 13, no.1, p. 90-92 (2009)
    • BookChapter
    Cerebral cavernous malformation
    Revencu, Nicole[UCL] Vikkula, Miikka[UCL] (2009) Encyclopedia of molecular mechanism of disease — [ISBN : 978-3-540-33445-3]