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Displaying 13 results.
    • Journal article
    Ligand oligomerization state controls Tie2 receptor trafficking and angiopoietin-2-specific responses.
    Pietilä, Riikka Nätynki, Marjut Tammela, Tuomas Kangas, Jaakko Pulkki, Kristina H Limaye, Nisha Vikkula, Miikka Koh, Gou Young Saharinen, Pipsa Alitalo, Kari Eklund, Lauri (2012) Journal of Cell Science — Vol. 125, no.Pt 9, p. 2212-23 (2012)
    • Speech
    Segregation of fluorescent membrane lipids into distinct micrometric domains: relevance for endogenous lipids and biogenesis in erythrocytes
    D'Auria, Ludovic[UCL] Aleksandrowicz, Paulina[UCL] Fenaux, Marisa[UCL] Van Der Smissen, Patrick[UCL] Chantrain, Christophe[UCL] Vermylen, Christiane[UCL] Vikkula, Miikka[UCL] Courtoy, Pierre J.[UCL] Tyteca, Donatienne[UCL] (2012) International Conference on Membrane Domains — Dijon, France
    • BookChapter
    Vascular Malformations
    Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2012) Fitzpatrick's Dermatology in General Medecine — [ISBN : 978-0-0716-6904-7]
    • Journal article
    Capillary Malformation-Arteriovenous Malformation Syndrome: A Report of 2 Cases, Diagnostic Criteria, and Management.
    Català, A Roé, E Vikkula, Miikka[UCL] Baselga, E (2012) Actas Dermo-Sifiliograficas — Vol. xxx, no.xx, p. xxx-xxx (2012)
    • BookChapter
    Vascular anomalies: from genetics toward models for therapeutic trials
    Uebelhoer, Mélanie[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2012) Angiogenesis: from development to pathology — [ISBN : 978-1-936113-43-9]
    • Journal article
    Génétique
    Vikkula, Miikka[UCL] (2012) Saint-Luc Magazine — no.19, p. 10-11 (Février-mars 2012)
    • Journal article
    Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
    Butler, Matthew G Dagenais, Susan L Garcia-Perez, José L Brouillard, Pascal Vikkula, Miikka Strouse, Peter Innis, Jeffrey W Glover, Thomas W (2012) American Journal of Medical Genetics. Part A — Vol. 158A, no.4, p. 839-49 (2012)
    • Report
    Direct-to-consumer genetic testing services
    Borry, Pascal Poirel, Hélène[UCL] Baatout, Sarah Blaumeiser, Bettina Cassiman, Jean-Jacques de Thibault de Boesinghe, Léopold Fondu, Michel Godderis, Lode Haufroid, Vincent[UCL] Hulstaert, Frank Kirsch-Volders, Micheline Liebaers, Inge Loeys, Bart Poppe, Bruce Schamps, Geneviève[UCL] Van Larebeke, Nicolas Van Nerom, Anne Van Oyen, Herman Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] (2012)
    • Journal article
    Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations.
    Jaureguiberry, Graciana De la Dure-Molla, Muriel Parry, David Quentric, Mickael Himmerkus, Nina Koike, Toshiyasu Poulter, James Klootwijk, Enriko Robinette, Steven L Howie, Alexander J Patel, Vaksha Figueres, Marie-Lucile Stanescu, Horia C Issler, Naomi Nicholson, Jeremy K Bockenhauer, Detlef Laing, Christopher Walsh, Stephen B McCredie, David A Povey, Sue Asselin, Audrey Picard, Arnaud Coulomb, Aurore Medlar, Alan J Bailleul-Forestier, Isabelle Verloes, Alain Le Caignec, Cedric Roussey, Gwenaelle Guiol, Julien Isidor, Bertrand Logan, Clare Shore, Roger Johnson, Colin Inglehearn, Christopher Al-Bahlani, Suhaila Schmittbuhl, Matthieu Clauss, François Huckert, Mathilde Laugel, Virginie Ginglinger, Emmanuelle Pajarola, Sandra Spartà, Giuseppina Bartholdi, Deborah Rauch, Anita Addor, Marie-Claude Yamaguti, Paulo M Safatle, Heloisa P Acevedo, Ana Carolina Martelli-Júnior, Hercílio dos Santos Netos, Pedro E Coletta, Ricardo D Gruessel, Sandra Sandmann, Carolin Ruehmann, Denise Langman, Craig B Scheinman, Steven J Ozdemir-Ozenen, Didem Hart, Thomas C Hart, P Suzanne Neugebauer, Ute Schlatter, Eberhard Houillier, Pascal Gahl, William A Vikkula, Miikka Bloch-Zupan, Agnès Bleich, Markus Kitagawa, Hiroshi Unwin, Robert J Mighell, Alan Berdal, Ariane Kleta, Robert (2012) Nephron. Physiology — Vol. 122, no.1-2, p. 1-6 (2012)
    • Journal article
    Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.
    Ostergaard, Pia Simpson, Michael A Mendola, Antonella[UCL] Vasudevan, Pradeep Connell, Fiona C van Impel, Andreas Moore, Anthony T Loeys, Bart L Ghalamkarpour, Arash Onoufriadis, Alexandros Martinez-Corral, Ines Devery, Sophie Leroy, Jules G van Laer, Lut Singer, Amihood Bialer, Martin G McEntagart, Meriel Quarrell, Oliver Brice, Glen Trembath, Richard C Schulte-Merker, Stefan Makinen, Taija Vikkula, Miikka Mortimer, Peter S Mansour, Sahar Jeffery, Steve (2012) American journal of human genetics — Vol. 90, no.2, p. 356-62 (2012)
    • Journal article
    Classification et génétique des malformations vasculaires
    Ballieux, F. Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2012) Archives de pédiatrie — Vol. 19, no. 6 SUPPL. 1 (2012)
    • Journal article
    Prevalence and spectrum of SDHx mutations in pheochromocytoma and paraganglioma in patients from Belgium: an update
    Persu, Alexandre[UCL] Lannoy, Nathalie[UCL] Maiter, Dominique[UCL] Mendola, Antonella[UCL] Montigny, Pauline[UCL] Oriot, Philippe Vinck, W. Garin, Pierre[UCL] Hamoir, Marc[UCL] Vikkula, Miikka[UCL] (2012) Hormone and Metabolic Research — Vol. 44, no. 5, p. 349-353 (2012)
    • Journal article
    TMEM165 Deficiency Causes a Congenital Disorder of Glycosylation.
    Foulquier, François Amyere, Mustapha Jaeken, Jaak Zeevaert, Renate Schollen, Els Race, Valérie Bammens, Riet Morelle, Willy Rosnoblet, Claire Legrand, Dominique Demaegd, Didier[UCL] Buist, Neil Cheillan, David Guffon, Nathalie Morsomme, Pierre[UCL] Annaert, Willem Freeze, Hudson H Van Schaftingen, Emile Vikkula, Miikka Matthijs, Gert (2012) American Journal of Human Genetics — Vol. 91, no. 1, p. 15-26 (2012)