Risultati della ricerca - Oscarson, Mikael

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  1. 1
    Late onset hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - how web searching by the family solved unexplained unconsciousness: a case report

    Late onset hyperornithinemia-hyperammonemia-homocitrullinuria syndrome - how web searching by the family solved unexplained unconsciousness: a case report di Silfverberg, Thomas, Sahlander, Fredrik, Enlund, Magnus, Oscarson, Mikael, Hårdstedt, Maria

    Pubblicazione 2018
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  2. 2
    The evolution of drug-activated nuclear receptors: one ancestral gene diverged into two xenosensor genes in mammals

    The evolution of drug-activated nuclear receptors: one ancestral gene diverged into two xenosensor genes in mammals di Handschin, Christoph, Blättler, Sharon, Roth, Adrian, Looser, Renate, Oscarson, Mikael, Kaufmann, Michel R, Podvinec, Michael, Gnerre, Carmela, Meyer, Urs A

    Pubblicazione 2004
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  3. 3
    Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA

    Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA di Barbaro, Michela, Balsamo, Antonio, Anderlid, Britt Marie, Myhre, Anne Grethe, Gennari, Monia, Nicoletti, Annalisa, Pittalis, Maria Carla, Oscarson, Mikael, Wedell, Anna

    Pubblicazione 2009
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  4. 4
    Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1

    Pituitary autoantibodies in autoimmune polyendocrine syndrome type 1 di Bensing, Sophie, Fetissov, Sergueï O., Mulder, Jan, Perheentupa, Jaakko, Gustafsson, Jan, Husebye, Eystein S., Oscarson, Mikael, Ekwall, Olov, Crock, Patricia A., Hökfelt, Tomas, Hulting, Anna-Lena, Kämpe, Olle

    Pubblicazione 2007
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  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 di 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

    Pubblicazione 2021
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