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Displaying 12 results.
    • Journal article
    Routine use of gene panel testing in hereditary breast cancer should be performed with caution
    van Marcke, Cédric[UCL] De Leener, Anne[UCL] Berlière, Martine[UCL] Vikkula, Miikka[UCL] Duhoux, François[UCL] (2017) CRC Critical Reviews in Oncology - Hematology — Vol. x, no.x, p. x (2017)
    • BookChapter
    Genetics of Arteriovenous Malformations
    Amyere, Mustapha[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2017) Brain Arteriovenous Malformations : Pathogenesis, Epidemiology, Diagnosis, Treatment and Outcome — [ISBN : 978-3-319-63963-5]
    • Journal article
    Germline Loss-of-Function Mutations in EPHB4 cause a Second Form of Capillary Malformation–Arteriovenous Malformation (CM-AVM2) deregulating RAS-MAPK signaling.
    Amyere, Mustapha[UCL] Revencu, Nicole[UCL] Helaers, Raphaël[UCL] Pairet, Eleonore[UCL] Baselga, Eulalia Cordisco, Maria Chung, Wendy Dubois, Josée Lacour, Jean-Philippe Martorell, Loreto Mazereeuw-Hautier, Juliette Pyeritz, Reed E. Amor, David J. Bisdorff, Anouck Blei, Francine Bombei, Hannah Dompmartin, Anne Brooks, David J. González-Enseñat, Maria Antonia Frieden, Ilona Gerard, Marion Kvarnung, Malin Kwan Hanson-Kahn, Andrea Hudgins, Louanne Leaute-Labreze, Christine McCuaig, Catherine Metry, Denise Parent, Philippe Paul, Carle Petit, Florence Phan, Alice Quere, Isabelle Salhi, Aicha Turner, Anne Vabres, Pierre Vicente, Asuncion Wargon, Orli Watanabe, Shoji Weibel, Lisa Wilson, Ashley Willing, Marcia Mulliken, John B. Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2017) Circulation — Vol. 136, no. 11, p. 1037-1048 (2017)
    • Journal article
    Loss of ADAMTS3 activity causes Hennekam lymphangiectasia-lymphedema syndrome 3
    Brouillard, Pascal[UCL] Dupont, Laura Helaers, Raphaël[UCL] Coulie, Richard[UCL] Tiller, George E. Peeden, Joseph Colige, Alain Vikkula, Miikka[UCL] (2017) Human Molecular Genetics — Vol. 26, no. 21, p. 4095-4104 (2017)
    • Journal article
    GATA2 null mutation associated with incomplete penetrance in a family with Emberger syndrome
    Brambila-Tapia, Aniel Jessica Leticia García-Ortiz, José Elías Brouillard, Pascal[UCL] Nguyen, Ha-Long[UCL] Vikkula, Miikka[UCL] Ríos-González, Blanca Estela Sandoval-Muñiz, Roberto de Jesús Sandoval-Talamantes, Ana Karen Bobadilla-Morales, Lucina Corona-Rivera, Jorge Román Arnaud-Lopez, Lisette (2017) Hematology — Vol. 22, no. 8, p. 467-71 (2017)
    • Journal article
    Comment on "Increased identification of candidates for high-risk breast cancer screening through expanded Genetic Testing"
    van Marcke, Cédric[UCL] Vikkula, Miikka[UCL] Duhoux, François[UCL] (2017) Journal of the American College of Radiology — Vol. 14, no. 5, p. 582 (2017)
    • BookChapter
    Venous malformations
    Boon, Laurence M.[UCL] Ballieux, Fanny[UCL] Vikkula, Miikka[UCL] (2017) Fitzpatrick's Dermatology in General Medicine, 9th edition — [ISBN : 0071669043]
    • BookChapter
    Venous malformations
    Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] Seront, Emmanuel[UCL] (2017) UpToDate — [ISBN : 1090-3496]
    • Journal article
    PDGFRB gain-of-function mutations in sporadic infantile myofibromatosis.
    Arts, Florence[UCL] Sciot, Raf Brichard, Bénédicte[UCL] Renard, Marleen de Rocca Serra, Audrey[UCL] Dachy, Guillaume[UCL] Noël, Laura A[UCL] Velghe, Amélie[UCL] Galant, Christine[UCL] Debiec-Rychter, Maria Van Damme, An[UCL] Vikkula, Miikka[UCL] Helaers, Raphaël[UCL] Limaye, Nisha[UCL] Antoine, Hélène[UCL] Demoulin, Jean-Baptiste[UCL] (2017) Human Molecular Genetics — Vol. 26, no. 10, p. 1801-1810 (2017)
    • Journal article
    Blue Rubber Bleb Nevus (BRBN) Syndrome Is Caused by Somatic TEK (TIE2) Mutations.
    Soblet, Julie[UCL] Kangas, Jaakko Nätynki, Marjut Mendola, Antonella[UCL] Helaers, Raphaël[UCL] Uebelhoer, Mélanie Kaakinen, Mika Cordisco, Maria Dompmartin, Anne Enjolras, Odile Holden, Simon Irvine, Alan D Kangesu, Loshan Léauté-Labrèze, Christine Lanoel, Agustina Lokmic, Zerina Maas, Saskia McAleer, Maeve A Penington, Anthony Rieu, Paul Syed, Samira van der Vleuten, Carine Watson, Rosemarie Fishman, Steven J Mulliken, John B Eklund, Lauri Limaye, Nisha Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2017) The Journal of Investigative Dermatology — Vol. 137, no. 1, p. 207-216 (2017)
    • Journal article
    KIF1B and NF1 are the most frequently mutated genes in paraganglioma tumors
    Evenepoel, Lucie[UCL] Helaers, Raphaël[UCL] Vroonen, Laurent Aydin, Selda[UCL] Hamoir, Marc[UCL] Maiter, Dominique[UCL] Vikkula, Miikka[UCL] Persu, Alexandre[UCL] (2017) Endocrine - Related Cancer — Vol. 24, no. 8, p. L57-L61 (2017)
    • BookChapter
    The genetic basis of vascular anomalies
    Nguyen, Ha-Long[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2017) Vascular anomalies for the hematologist/oncologist —