Shohreh Issazadeh-Navikas

Shohreh Issazadeh-Navikas

Professor


  1. 2020
  2. Published

    A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family

    Darbari, E., Zare-Abdollahi, D., Alavi, A., Rezaei Kanavi, M., Feizi, S., Hosseini, S. B., Baradaran-Rafii, A., Ahmadieh, H., Issazadeh-Navikas, Shohreh & Elahi, E., 2020, In: Molecular Vision. 26, p. 757-765 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Antiviral, Immunomodulatory and Antiproliferative Activities of Recombinant Soluble IFNAR2 without IFN-ß Mediation

    Hurtado Guerrero, Isaac, Hernáez, B., Pinto-medel, M. J., Calonge, E., Rodriguez-bada, J. L., Urbaneja, P., Alonso, A., Mena-vázquez, N., Aliaga, P., Issazadeh-Navikas, Shohreh, Pavia, J., Leyva, L., Alcamí, J., Alcamí, A., Fernández, Ó. & Oliver-martos, B., 2020, In: Journal of Clinical Medicine. 9, 4, p. 959

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    CHST6 mutations identified in Iranian MCD patients and CHST6 mutations reported worldwide identify targets for gene editing approaches including the CRISPR/Cas system

    Safari, Iman, Baradaran-Rafii, A., Issazadeh-Navikas, Shohreh & Elahi, E., 2020, In: International Ophthalmology. 40, p. 2223-2235

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published
  6. Published

    Pharmacological inhibition of carnitine palmitoyl transferase 1 inhibits and reverses experimental autoimmune encephalitis in rodents

    Mørkholt, A. S., Oklinski, M. K., Larsen, A., Bockermann, R., Issazadeh-Navikas, Shohreh, Nieland, J. G. K., Kwon, T., Corthals, A., Nielsen, S. & Nieland, J. D. V., 2020, In: PLoS ONE. 15, 6, p. e0234493

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 3998988