检索结果 - Miikka Vikkula

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  1. 1
    Pathogenesis of Vascular Anomalies

    Pathogenesis of Vascular Anomalies 由 Laurence M. Boon, Fanny Ballieux, Miikka Vikkula

    出版 2010
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  2. 2
    Vascular Anomalies: From Genetics toward Models for Therapeutic Trials

    Vascular Anomalies: From Genetics toward Models for Therapeutic Trials 由 Mélanie Uebelhoer, Laurence M. Boon, Miikka Vikkula

    出版 2012
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  3. 3
    Venous malformation: update on aetiopathogenesis, diagnosis and management

    Venous malformation: update on aetiopathogenesis, diagnosis and management 由 A. Dompmartin, Miikka Vikkula, Laurence M. Boon

    出版 2010
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  4. 4
    Genetics of lymphatic anomalies

    Genetics of lymphatic anomalies 由 Pascal Brouillard, Laurence M. Boon, Miikka Vikkula

    出版 2014
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  5. 5
    From germline towards somatic mutations in the pathophysiology of vascular anomalies

    From germline towards somatic mutations in the pathophysiology of vascular anomalies 由 Nisha Limaye, Laurence M. Boon, Miikka Vikkula

    出版 2009
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  6. 6
    Vascular Anomalies Caused by Abnormal Signaling within Endothelial Cells: Targets for Novel Therapies

    Vascular Anomalies Caused by Abnormal Signaling within Endothelial Cells: Targets for Novel Therapies 由 Ha‐Long Nguyen, Laurence M. Boon, Miikka Vikkula

    出版 2017
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  7. 7
    Genetic Basis and Therapies for Vascular Anomalies

    Genetic Basis and Therapies for Vascular Anomalies 由 Angela Queisser, Emmanuel Seront, Laurence M. Boon, Miikka Vikkula

    出版 2021
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  8. 8
    Lymphatic Malformations: Genetics, Mechanisms and Therapeutic Strategies

    Lymphatic Malformations: Genetics, Mechanisms and Therapeutic Strategies 由 Taija Mäkinen, Laurence M. Boon, Miikka Vikkula, Kari Alitalo

    出版 2021
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  9. 9
    Extracranial arteriovenous malformations: towards etiology-based therapeutic management

    Extracranial arteriovenous malformations: towards etiology-based therapeutic management 由 Julien Coulie, Emmanuel Seront, Miikka Vikkula, Laurence M. Boon

    出版 2025
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  10. 10
    Inheritance Patterns of Infantile Hemangioma

    Inheritance Patterns of Infantile Hemangioma 由 Eeva Castrén, Päivi Salminen, Miikka Vikkula, Anne Pitkäranta, Tuomas Klockars

    出版 2016
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  11. 11
    Variable Somatic <b><i>TIE2</i></b> Mutations in Half of Sporadic Venous Malformations

    Variable Somatic <b><i>TIE2</i></b> Mutations in Half of Sporadic Venous Malformations 由 Julie Soblet, Nisha Limaye, Mélanie Uebelhoer, Laurence M. Boon, Miikka Vikkula

    出版 2013
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  12. 12
    Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase

    Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase 由 Alexandre Irrthum, Marika J. Karkkainen, Koenraad Devriendt, Kari Alitalo, Miikka Vikkula

    出版 2000
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  13. 13
    Theranostic Advances in Vascular Malformations

    Theranostic Advances in Vascular Malformations 由 Valérie Dekeuleneer, Emmanuel Seront, An Van Damme, Laurence M. Boon, Miikka Vikkula

    出版 2020
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  14. 14
    Locus for susceptibility for familial capillary malformation (‘port-wine stain’) maps to 5q

    Locus for susceptibility for familial capillary malformation (‘port-wine stain’) maps to 5q 由 Iiro Eerola, Laurence M. Boon, Shôji Watanabe, Henri Grynberg, John B. Mulliken, Miikka Vikkula

    出版 2002
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  15. 15
    A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations

    A review of mechanisms of disease across PIK3CA-related disorders with vascular manifestations 由 Guillaume Canaud, Adrienne M. Hammill, Denise M. Adams, Miikka Vikkula, Kim M. Keppler‐Noreuil

    出版 2021
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  16. 16
    KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation

    KITLG Mutations Cause Familial Progressive Hyper- and Hypopigmentation 由 Mustapha Amyere, Thomas Vogt, Joe J. Hoo, F Brandrup, Anette Bygum, Laurence M. Boon, Miikka Vikkula

    出版 2011
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  17. 17
    Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population

    Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population 由 Michella Ghassibe‐Sabbagh, Bénédicte Bayet, Nicole Revençu, Christine Verellen‐Dumoulin, Y. Gillerot, R Vanwijck, Miikka Vikkula

    出版 2005
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  18. 18
    A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

    A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? 由 Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, Thierry Sluysmans, Koenraad Devriendt, Han G. Brunner, Miikka Vikkula

    出版 2006
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  19. 19
    Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3

    Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3 由 Pascal Brouillard, Laura Dupont, Raphaël Helaers, Richard Coulie, George E. Tiller, Joseph Peeden, Alain Colige, Miikka Vikkula

    出版 2017
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  20. 20
    Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus

    Targeted treatment in complex lymphatic anomaly: a case of synergistic efficacy of trametinib and sirolimus 由 Emmanuel Seront, Antoine Froidure, Nicole Revençu, Valérie Dekeuleneer, Philippe Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M. Boon

    出版 2024
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