Search Results - Basargina, EN

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  1. 1
    175 Very rare case of Noonan syndrome, type 2

    175 Very rare case of Noonan syndrome, type 2 by Gandaeva, LA, Zhurkova, NV, Basargina, EN, Pushkov, AA, Degtayreva, TD, Miroshnichenko, VP, Kondakova, OB, Savostyanov, KV

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  2. 2
    P771P36 deletion syndrome in children with cardiomyopathy: two clinical cases

    P771P36 deletion syndrome in children with cardiomyopathy: two clinical cases by Zhurkova, N V, Pushkov, A A, Savostyanov, K V, Basargina, EN, Pakhomov, A V, Ermolenko, V S, Derevianina, Y V

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  3. 3
    GP33 High prevalence noonan syndrome in russian children with hypertrophic cardiomyopathy, diagnosed by next generation sequencing

    GP33 High prevalence noonan syndrome in russian children with hypertrophic cardiomyopathy, diagnosed by next generation sequencing by Zhurkova, N, Savostyanov, K, Pushkov, AA, Vashakmadze, ND, Fedorova, N, Zharova, OP, Gandaeva, LA, Sdvigova, NA, Kondakova, OB, Basargina, EN

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  4. 4
    P77 1P36 deletion syndrome in children with cardiomyopathy: two clinical cases

    P77 1P36 deletion syndrome in children with cardiomyopathy: two clinical cases by Zhurkova, NV, Pushkov, AA, Savostyanov, KV, Basargina, EN, Pakhomov, AV, Ermolenko, VS, Derevianina, YV

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  5. 5
    Biochemical and immunological markers of insufficiency of blood circulation in children with cardiomyopathies

    Biochemical and immunological markers of insufficiency of blood circulation in children with cardiomyopathies by Bershova, T. V., Shmatkova, Yu. V., Ivanov, A. P., Bakanov, M. I., Basargina, E. N., Zurabova, R. B., Monaenkova, S. V., Gerasimova, Yu. V.

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