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1. • Journal article

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   Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.

   Gong, Y Vikkula, Miikka[UCL] Boon, L Liu, J Beighton, P Ramesar, R Peltonen, L Somer, H Hirose, T Dallapiccola, B De Paepe, A Swoboda, W Zabel, B Superti-Furga, A Steinmann, B Brunner, H G Jans, A Boles, R G Adkins, W van den Boogaard, M J Olsen, B R Warman, M L (1996) American journal of human genetics — Vol. 59, no.1, p. 146-51 (1996)
2. • Journal article

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   Overrepresentation of missense mutations in mild hemophilia A patients from Belgium: founder effect or independent occurrence?

   Lannoy, Nathalie[UCL] Lambert, Catherine[UCL] Vikkula, Miikka[UCL] Hermans, Cédric[UCL] (2015) Thrombosis Research : vascular obstruction, hemorrhage and hemostasis — Vol. 135, no. 6, p. 1057-1063 (2015)
3. • Journal article

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   Inheritance Patterns of Infantile Hemangioma.

   Castrén, Eeva Salminen, Päivi Vikkula, Miikka[UCL] Pitkäranta, Anne Klockars, Tuomas (2016) Pediatrics — Vol. 138, no. 5, p. e20161623 [1-9] (2016)
4. • Journal article

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   Ureteropelvic junction obstruction with primary lymphoedema associated with<i>CELSR1</i>variants

   Alpaslan, Murat[UCL] Mestré-Godin, Sandrine Lay, Aurélie Giacalone, Guido[UCL] Helaers, Raphaël[UCL] Adham, Salma[UCL] Kovacsik, Hélène Guillemard, Sophie Mercier, Erick Boon, Laurence M.[UCL] Revencu, Nicole[UCL] Brouillard, Pascal[UCL] Quere, Isabelle Vikkula, Miikka[UCL] (2023) Journal of Medical Genetics — Vol. x, no.x, p. jmg-2023-109171 (2023)
5. • Journal article

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   Increased Collagen Turnover Is a Feature of Fibromuscular Dysplasia and Associated With Hypertrophic Radial Remodeling: A Pilot, Urine Proteomic Study.

   Latosinska, Agnieszka Bruno, Rosa Maria Pappaccogli, Marco[UCL] Bacca, Alessandra Beauloye, Christophe[UCL] Boutouyrie, Pierre Khettab, Hakim Staessen, Jan A Taddei, Stefano Toubiana, Laurent Vikkula, Miikka[UCL] Mischak, Harald Persu, Alexandre[UCL] (2022) Hypertension — Vol. 79, no. 1, p. 93-103 (2022)
6. • Journal article

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   GNA11-mutated Sturge–Weber syndrome has distinct neurological and dermatological features

   Dompmartin, Anne van der Vleuten, Carine J. M. Dekeuleneer, Valérie[UCL] Duprez, Thierry[UCL] Revencu, Nicole[UCL] Désir, Julie te Loo, D. Maroeska W. M. Flucke, Uta Eijkelenboom, Astrid Schultze Kool, Leo Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2022) European journal of neurology — Vol. 29, no. 10, p. 3061-3070 (2022)
7. • Journal article

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   The VASCERN-VASCA Working Group Diagnostic and Management Pathways for Venous Malformations

   Dompmartin, Anne Baselga, Eulalia Boon, Laurence M.[UCL] Diociaiuti, Andrea Dvorakova, Veronika El Hachem, May Gasparella, Paolo Haxhija, Emir Ghaffarpour, Nader Kyrklund, Kristiina Irvine, Alan D. Kapp, Friedrich G. Rößler, Jochen Salminen, Päivi van den Bosch, Caroline van der Vleuten, Carine Schultze Kool, Leo Vikkula, Miikka[UCL] (2023) Journal of Vascular Anomalies — Vol. 4, no.2, p. e064 (2023)
8. • Journal article

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   Molecular Pathways and Possible Therapies for Head and Neck Vascular Anomalies.

   Coulie, Julien[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2022) Journal of oral pathology & medicine — Vol. 51, no. 10, p. 878-887 (2022)
9. • Journal article

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   Heredity of port-wine stains: investigation of families without a RASA1 mutation.

   Troilius Rubin, Agneta Lauritzen, Edgar Ljunggren, Bo Revencu, Nicole[UCL] Vikkula, Miikka[UCL] Svensson, Åke (2015) Journal of Cosmetic and Laser Therapy — Vol. 17, no.4, p. 204-208 (2015)
10. • Journal article

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    Radio-opaque ethylcellulose-ethanol is a safe and efficient sclerosing agent for venous malformations.

    Dompmartin, Anne Blaizot, Xavier Théron, Jacques Hammer, Frank[UCL] Chene, Yannick Labbé, Daniel Barrellier, Marie-Thérèse Gaillard, Cathy Leroyer, Robert Chedru, Valérie Ollivier, Catherine Vikkula, Miikka Boon, Laurence M.[UCL] (2011) European Radiology — Vol. 21, no. 12, p. 2647-2656 (2011)
11. • Speech

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    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
12. • BookChapter

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    Vascular Malformations

    Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2012) Fitzpatrick's Dermatology in General Medecine — [ISBN : 978-0-0716-6904-7]
13. • Journal article

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    Cerebrovascular disorders: molecular insights and therapeutic opportunities.

    Storkebaum, Erik Quaegebeur, Annelies Vikkula, Miikka Carmeliet, Peter (2011) Nature Neuroscience — Vol. 14, no.11, p. 1390-7 (2011)
14. • Journal article

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    Venous malformation: update on aetiopathogenesis, diagnosis and management.

    Dompmartin, A Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] (2010) Phlebology — Vol. 25, no.5, p. 224-35 (2010)
15. • Journal article

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    Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

    Vikkula, Miikka[UCL] Boon, Laurence M.[UCL] Carraway, K L Calvert, J T Diamonti, A J Goumnerov, B Pasyk, K A Marchuk, D A Warman, M L Cantley, L C Mulliken, J B Olsen, B R (1996) Cell — Vol. 87, no.7, p. 1181-90 (1996)
16. • Journal article

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    Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome

    Pansuriya, Twinkal C van Eijk, Ronald d'Adamo, Pio van Ruler, Maayke A J H Kuijjer, Marieke L Oosting, Jan Cleton-Jansen, Anne-Marie van Oosterwijk, Jolieke G Verbeke, Sofie L J Meijer, Daniëlle van Wezel, Tom Nord, Karolin H Sangiorgi, Luca Toker, Berkin Liegl-Atzwanger, Bernadette San-Julian, Mikel Sciot, Raf Limaye, Nisha[UCL] Kindblom, Lars-Gunnar Daugaard, Soeren Godfraind, Catherine[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] Kurek, Kyle C Szuhai, Karoly French, Pim J Bovée, Judith V M G (2011) Nature Genetics — Vol. 43, no. 12, p. 1256-61 (2011)
17. • Journal article

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    Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome.

    Bowen, Margot E Boyden, Eric D Holm, Ingrid A Campos-Xavier, Belinda Bonafé, Luisa Superti-Furga, Andrea Ikegawa, Shiro Cormier-Daire, Valerie Bovée, Judith V Pansuriya, Twinkal C de Sousa, Sérgio B Savarirayan, Ravi Andreucci, Elena Vikkula, Miikka[UCL] Garavelli, Livia Pottinger, Caroline Ogino, Toshihiko Sakai, Akinori Regazzoni, Bianca M Wuyts, Wim Sangiorgi, Luca Pedrini, Elena Zhu, Mei Kozakewich, Harry P Kasser, James R Seidman, Jon G Kurek, Kyle C Warman, Matthew L (2011) PLoS Genetics — Vol. 7, no.4, p. e1002050 (2011)
18. • Journal article

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    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)
19. • Journal article

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    The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3.

    Jüppner, H Schipani, E Bastepe, M Cole, D E Lawson, M L Mannstadt, M Hendy, G N Plotkin, H Koshiyama, H Koh, T Crawford, J D Olsen, B R Vikkula, Miikka[UCL] (1998) Proceedings of the National academy of sciences of the United States of America — Vol. 95, no.20, p. 11798-803 (1998)
20. • Journal article

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    KITLG mutations cause familial progressive hyper- and hypopigmentation

    Amyere, Mustapha[UCL] Vogt, Thomas Hoo, Joe Brandrup, Flemming Bygum, Anette Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2011) The Journal of Investigative Dermatology — Vol. 131, no. 6, p. 1234-1239 (2011)
21. • BookChapter

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    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]
22. • BookChapter

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    Arteriovenous malformation in mice and men

    Revencu, Nicole[UCL] Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2008) Tumor angiogenesis — [ISBN : 978-3-540-33176-6]
23. • BookChapter

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    Vascular matrix and disorders

    Karttunen, Leena Felbor, Ute Vikkula, Miikka[UCL] Olsen, Bjorn R. (2001) Hematopoiesis: A Developmental Approach — [ISBN : 978-0-1951-2450-7]
24. • BookChapter

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    Vascular Anomalies

    Boon, Laurence M.[UCL] Vikkula, Miikka[UCL] (2008) Fitzpatrick’s Dermatology in General Medicine — [ISBN : 978-0-07-149443-4]
25. • Journal article

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    Severe congenital lymphedema not caused by mutations in known lymphedema genes

    Greenberger, Shoshana Reznik-Wolf, H Ghalamkarpour, Arash[UCL] Marek-Yagel, D Vikkula, Miikka[UCL] Pras, E (2010) British Journal of Dermatology — Vol. 163, no. 6, p. 1346-1368 (2010)

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