Showing 1 - 3 results of 3 for search 'D. V. Kassina', query time: 0.02s Refine Results
  1. 1
    Intellectual development disorder syndrome with congenital anomalies of type 99, faceted female (OMIM: 300968), updated mutation in the USP9X gene

    Intellectual development disorder syndrome with congenital anomalies of type 99, faceted female (OMIM: 300968), updated mutation in the USP9X gene by A. Sh. Latypov, E. V. Proskurin, O. P. Sidorova, I. A. Vasilenko, D. V. Kassina, M. S. Bunak

    Published 2025-01-01
    Get full text
    Article
  2. 2
    Mitochondrial disorders in patients with familial form of MERRF syndrome

    Mitochondrial disorders in patients with familial form of MERRF syndrome by A. Sh. Latypov, E. V. Proskurina, S. V. Kotov, O. P. Sidorova, I. A. Vasilenko, D. V. Kassina, A. S. Kotov

    Published 2024-01-01
    Get full text
    Article
  3. 3
    Neutrophil extracellular traps as a promising marker of poor prognosis in operated patients with infective endocarditisarditis.

    Neutrophil extracellular traps as a promising marker of poor prognosis in operated patients with infective endocarditisarditis. by E. O. Kotova, A. Yu. Moiseeva, Zh. D. Kobalava, A. S. Pisyaryuk, D. V. Kassina, A. S. Gur’ev, T. A. Gusarova

    Published 2024-08-01
    Get full text
    Article

Search Tools: