Search Results - Freya Droege

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  1. 1

    Hypoxia-Inducible Factor–Prolyl Hydroxylase Inhibitor Improves Leukocyte Energy Metabolism in Hereditary Hemorrhagic Telangiectasia by Yves Schild, Jonah Bosserhoff, Freya Droege, Elisabeth Littwitz-Salomon, Joachim Fandrey, Anna Wrobeln

    Published in Life (2023-08-01)
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  2. 2

    Nationwide Awareness Campaign and Call for Dental Screening for Hereditary Hemorrhagic Telangiectasia in Germany by Urban W. Geisthoff, Frank Hölzle, Boris A. Stuck, Joachim Jackowski, Catherine Hand Goetz, Christina Grabowski, Freya Droege

    Published in International Journal of Dentistry (2023-01-01)
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  3. 3

    Prognostic Role of Blood NETosis in the Progression of Head and Neck Cancer by Anna Sophie Decker, Ekaterina Pylaeva, Alexandra Brenzel, Ilona Spyra, Freya Droege, Timon Hussain, Stephan Lang, Jadwiga Jablonska

    Published in Cells (2019-08-01)
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  4. 4

    Prevention of serious infections in hereditary hemorrhagic telangiectasia: roles for prophylactic antibiotics, the pulmonary capillaries-but not vaccination by Claire Shovlin, Kathleen Bamford, Carlo Sabbà, Hans-Jurgen Mager, Anette Kjeldsen, Freya Droege, Elisabetta Buscarini, Sophie Dupuis-Girod

    Published in Haematologica (2019-02-01)
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  5. 5

    Family planning, sexual activity and contraception in hereditary hemorrhagic telangiectasia: a European survey study by Josefien Hessels, Marco C. Post, Sanne Boerman, Freya Droege, Olivier Dupuis, ePAG, Urban W. Geisthoff, Pernille D. Haahr, Anette D. Kjeldsen, Johannes-Jurgen Mager, Sophie Dupuis-Girod, Elisabetta Buscarini

    Published in Orphanet Journal of Rare Diseases (2025-08-01)
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  6. 6

    Cobalamin and iron deficiency still presents a challenge in hereditary hemorrhagic telangiectasia by Marie Carolin Schleupner, Alexander Röth, Luise Adam, Nadia Sadok, Felicia Toppe, Antonia Klara Lakomek, Sami Wainwright, Noemi Voss, Lukas Boosfeld, Christina Kaiser, Julia Garvert, Stephan Lang, Urban Geisthoff, Freya Droege

    Published in Scientific Reports (2025-08-01)
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  7. 7

    European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT) by Omer F. Eker, Edoardo Boccardi, Ulrich Sure, Maneesh C. Patel, Saverio Alicante, Ali Alsafi, Nicola Coote, Freya Droege, Olivier Dupuis, Annette Dam Fialla, Bryony Jones, Ujwal Kariholu, Anette D. Kjeldsen, David Lefroy, Gennaro M. Lenato, Hans Jurgen Mager, Guido Manfredi, Troels H. Nielsen, Fabio Pagella, Marco C. Post, Catherine Rennie, Carlo Sabbà, Patrizia Suppressa, Pernille M. Toerring, Sara Ugolini, Elisabetta Buscarini, Sophie Dupuis-Girod, Claire L. Shovlin

    Published in Orphanet Journal of Rare Diseases (2020-06-01)
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