Treffer 1 - 3 von 3 für Suche 'Rod, Raya', Suchdauer: 0,35s Treffer weiter einschränken
  1. 1
    A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis

    A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis von Zivony-Elboum, Yifat, Westbroek, Wendy, Kfir, Nehama, Savitzki, David, Shoval, Yishay, Bloom, Assnat, Rod, Raya, Khayat, Morad, Gross, Bella, Samri, Walid, Cohen, Hector, Sonkin, Vadim, Freidman, Tatiana, Geiger, Dan, Fattal-Valevski, Aviva, Anikster, Yair, Waters, Aoife M, Kleta, Robert, Falik-Zaccai, Tzipora C

    Veröffentlicht in Journal of medical genetics

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  2. 2
    Amyloid β synaptotoxicity is Wnt-PCP dependent and blocked by fasudil

    Amyloid β synaptotoxicity is Wnt-PCP dependent and blocked by fasudil von Sellers, Katherine J., Elliott, Christina, Jackson, Joshua, Ghosh, Anshua, Ribe, Elena, Rojo, Ana I., Jarosz-Griffiths, Heledd H., Watson, Iain A., Xia, Weiming, Semenov, Mikhail, Morin, Peter, Hooper, Nigel M., Porter, Rod, Preston, Jane, Al-Shawi, Raya, Baillie, George, Lovestone, Simon, Cuadrado, Antonio, Harte, Michael, Simons, Paul, Srivastava, Deepak P., Killick, Richard

    Veröffentlicht in Alzheimer's & dementia

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  3. 3
    Efficacy of Palivizumab Immunoprophylaxis for Reducing Severe RSV Outcomes in Children with Immunodeficiencies: A Systematic Review

    Efficacy of Palivizumab Immunoprophylaxis for Reducing Severe RSV Outcomes in Children with Immunodeficiencies: A Systematic Review von Reicherz, Frederic, Abu-Raya, Bahaa, Akinseye, Omolabake, Rassekh, Shahrad Rod, Wiens, Matthew O, Lavoie, Pascal M


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