Search Results - "Nord, DG"

  • Showing 1 - 6 results of 6
Refine Results
  1. 1
    Intrauterine vertical SARS‐CoV‐2 infection: a case confirming transplacental transmission followed by divergence of the viral genome

    Intrauterine vertical SARS‐CoV‐2 infection: a case confirming transplacental transmission followed by divergence of the viral genome by Zaigham, M, Holmberg, A, Karlberg, ML, Lindsjö, OK, Jokubkiene, L, Sandblom, J, Strand, AS, Andersson, O, Hansson, SR, Nord, DG, Tannenberg, P

    “…This article includes Author Insights, a video available at https://vimeo.com/bjog/authorinsights16682…”
    Get full text
    Journal Article
    Save to List
    Saved in:
  2. 2
    Imprinting relaxation of an ovarian dysgerminoma in a patient with Prader-Willi syndrome

    Imprinting relaxation of an ovarian dysgerminoma in a patient with Prader-Willi syndrome by Gonzalez, CM, Wessman, S, Tesi, B, Taylan, F, McCluggage, G, Kuchinskaya, E, Poluha, A, Holm, S, Nargard, R, de Stahl, TD, Nord, DG, Lagerstedt, K, Nordgren, A

    Get full text
    Conference Proceeding
    Save to List
    Saved in:
  3. 3
    THE IMMUNE CELL ATLAS OF HUMAN NEUROBLASTOMA

    THE IMMUNE CELL ATLAS OF HUMAN NEUROBLASTOMA by Verhoeven, BM, Mei, S, Olsen, T, Gustafsson, K, Valind, A, Nord, DG, Fard, S, Hagerling, C, Kharchenko, P, Kogner, P, Johnsen, JI, Baryawno, N

    Published in PEDIATRIC BLOOD & CANCER (2022)
    Get full text
    Conference Proceeding
    Save to List
    Saved in:
  4. 4
    Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model

    Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model by Tegelberg, Saara, Tomašić, Nikica, Kallijärvi, Jukka, Purhonen, Janne, Elmér, Eskil, Lindberg, Eva, Nord, David Gisselsson, Soller, Maria, Lesko, Nicole, Wedell, Anna, Bruhn, Helene, Freyer, Christoph, Stranneheim, Henrik, Wibom, Rolf, Nennesmo, Inger, Wredenberg, Anna, Eklund, Erik A, Fellman, Vineta

    Published in Orphanet journal of rare diseases (20-04-2017)
    “…Mitochondrial diseases due to defective respiratory chain complex III (CIII) are relatively uncommon. The assembly of the eleven-subunit CIII is completed by…”
    Get full text
    Journal Article
    Save to List
    Saved in:
  5. 5
    Diagnostic yield and short-term clinical implications of nationwide germline whole genome sequencing in 280 children with solid tumors

    Diagnostic yield and short-term clinical implications of nationwide germline whole genome sequencing in 280 children with solid tumors by Tesi, B, Taylan, F, Lagerstedt-Robinson, K, Abel, F, Hellberg, M, de Stahl, TD, Wessman, S, Samuelsson, S, Henning, K, Frisk, T, Sabel, M, Vogt, H, Nyman, P, Giraud, G, Wille, J, Pronk, CJ, Nystrom, UN, Borssen, M, Fili, M, Stalhammar, G, Herold, N, Orrsjo, S, Poluha, A, Gonzalez, CM, Arvidsson, L, Rosen, A, Ekholm, K, Kuchinskaya, E, Hallbeck, AL, Shamikh, A, Mertens, F, Brandell, RR, Tham, E, Grillner, P, Sandgren, J, Ljungman, G, Nord, DG, Nordgren, A

    Get full text
    Conference Proceeding
    Save to List
    Saved in:
  6. 6
    The immune cell atlas of human neuroblastoma

    The immune cell atlas of human neuroblastoma by Verhoeven, BM, Mei, SL, Olsen, TK, Gustafsson, KK, Valind, A, Lindstrom, A, Nord, DG, Fard, SS, Hagerling, C, Kharchenko, PV, Kogner, P, Johnsen, JI, Baryawno, N

    Published in CANCER RESEARCH (2022)
    Get full text
    Conference Proceeding
    Save to List
    Saved in:

Search Tools: