The Combination of Chromosomal Reorganization and Inherited Point Mutation Has Led to the Development of a Rare Clinical Phenotype in a Patient with Disorder of Sex Differentiation... by Popovych, L. V., Shatillo, A. V., Zelinska, N. B., Tavokina, L. V., Gorodna, O. V., Livshits, G. B., Sirokha, D. A., Livshits, L. A.

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Physiological and behavioural implications of the portosystemic shunt in C57Bl/6J mice by Lehtimäki, Kimmo K., Rytkönen, Jussi, Pussinen, Raimo, Shatillo, Artem, Bragge, Timo, Heikkinen, Taneli, Fischer, David F., Kopanitsa, Maksym V., Sweeney, Patrick, Nurmi, Antti, Puoliväli, Jukka

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Cognitive disturbances in the cuprizone model of multiple sclerosis by Kopanitsa, Maksym V., Lehtimäki, Kimmo K., Forsman, Markku, Suhonen, Ari, Koponen, Juho, Piiponniemi, Tuukka O., Kärkkäinen, Anna‐Mari, Pavlidi, Pavlina, Shatillo, Artem, Sweeney, Patrick J., Merenlender‐Wagner, Avia, Kaye, Joel, Orbach, Aric, Nurmi, Antti

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EP.61DMD gene molecular genetic characterization in Eastern Europe and non European countries by Selvatici, R., Trabanelli, C., Buldrini, B., Fini, S., Gualandi, F., Rimessi, P., Neri, M., Fortunato, F., Potulska, A., Emandi, A., Lehman, I., Herczegfalvi, A., Guergueltcheva, V., Kyriakides, T., Sifi, Y., Molnar, M., Burnyte, B., Shatillo, A., Vlodavets, D., Ferlini, A.

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Kinin formation in the plasma and cerebral blood flow under conditions of cerebral ischemia/reperfusion in rats during modulation of kinin system activity by Orobei, M. V, Kulikov, V. P, Shatillo, Y. G

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