Search Results - Malin Oscarson

  • Showing 1 - 5 results of 5
Refine Results
  1. 1
    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus)

    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus) by Harjen, Hannah J, Hellum, Marit, Rørtveit, Runa, Oscarson, Malin, Anfinsen, Kristin P, Moldal, Elena R, Solbak, Susanna, Kanse, Sandip M, Henriksson, Carola E

    Published in PloS one
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Case report: Haemophagocytic histiocytic sarcoma in an english setter

    Case report: Haemophagocytic histiocytic sarcoma in an english setter by Kerboeuf, Mikael, Brun‐Hansen, Hege, Oscarson, Malin, Sjetne Lund, Heidi

    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  3. 3
    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus)

    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus) by Hannah J. Harjen, Marit Hellum, Runa Rørtveit, Malin Oscarson, Kristin P. Anfinsen, Elena R. Moldal, Susanna Solbak, Sandip M. Kanse, Carola E. Henriksson

    Published in PloS one
    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus)

    Persistent hypercoagulability in dogs envenomated by the European adder (Vipera berus berus) by Harjen, Hannah Jayne, Hellum, Marit Synnøve, Rørtveit, Runa, Oscarson, Malin, Anfinsen, Kristin Paaske, Moldal, Elena Regine, Solbak, Susanna, Kanse, Sandip, Henriksson, Carola Elisabeth

    Request full text
    Article
    Save to List
    Saved in:
  5. 5
    Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

    Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients by Stranneheim, Henrik, Lagerstedt-Robinson, Kristina, Magnusson, Måns, Kvarnung, Malin, Nilsson, Daniel, Lesko, Nicole, Engvall, Martin, Anderlid, Britt-Marie, Arnell, Henrik, Johansson, Carolina Backman, Barbaro, Michela, Björck, Erik, Bruhn, Helene, Eisfeldt, Jesper, Freyer, Christoph, Grigelioniene, Giedre, Gustavsson, Peter, Hammarsjö, Anna, Hellström-Pigg, Maritta, Iwarsson, Erik, Jemt, Anders, Laaksonen, Mikael, Enoksson, Sara Lind, Malmgren, Helena, Naess, Karin, Nordenskjöld, Magnus, Oscarson, Mikael, Pettersson, Maria, Rasi, Chiara, Rosenbaum, Adam, Sahlin, Ellika, Sardh, Eliane, Stödberg, Tommy, Tesi, Bianca, Tham, Emma, Thonberg, Håkan, Töhönen, Virpi, von Döbeln, Ulrika, Vassiliou, Daphne, Vonlanthen, Sofie, Wikström, Ann-Charlotte, Wincent, Josephine, Winqvist, Ola, Wredenberg, Anna, Ygberg, Sofia, Zetterström, Rolf H, Marits, Per, Soller, Maria Johansson, Nordgren, Ann, Wirta, Valtteri, Lindstrand, Anna, Wedell, Anna

    Published in Genome medicine
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:

Search Tools: