Hasil Pencarian - Evgeny V Vasilyev

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  1. 1
    High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism.

    High frequency of mutations in 'dyshormonogenesis genes' in severe congenital hypothyroidism. oleh Nina Makretskaya, Olga Bezlepkina, Anna Kolodkina, Alexey Kiyaev, Evgeny V Vasilyev, Vasily Petrov, Svetlana Kalinenkova, Oleg Malievsky, Ivan I Dedov, Anatoly Tiulpakov

    Diterbitkan 2018-01-01
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  2. 2
    A synonymous variant in GCK gene as a cause of gestational diabetes mellitus

    A synonymous variant in GCK gene as a cause of gestational diabetes mellitus oleh Natalia A. Zubkova, Petr M. Rubtsov, Fatima F. Burumkulova, Liudmila I. Ibragimova, Nina A. Makretskaya, Evgeny V. Vasilyev, Vasily M. Petrov, Anatoly N. Tiulpakov

    Diterbitkan 2019-06-01
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  3. 3
    Erratum: a synonymous variant in GCK gene as a cause of gestational diabetes mellitus (diabetes mellitus. 2019;22(2). Doi: 10.14341/dm9938)

    Erratum: a synonymous variant in GCK gene as a cause of gestational diabetes mellitus (diabetes mellitus. 2019;22(2). Doi: 10.14341/dm9938) oleh Natalia A. Zubkova, Petr M. Rubtsov, Fatima F. Burumkulova, Liudmila I. Ibragimova, Nina A. Makretskaya, Evgeny V. Vasilyev, Vasily M. Petrov, Anatoly N. Tiulpakov

    Diterbitkan 2019-10-01
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  4. 4
    Mutations in transcription factor as rare causes of diabetes in pregnancy

    Mutations in transcription factor as rare causes of diabetes in pregnancy oleh Natalia A. Zubkova, Fatima F. Burumkulova, Vasily A. Petrukhin, Margarita A. Plechanova, Anton E. Panov, Evgeny V. Vasilyev, Vasily M. Petrov, Nina A. Makretskaya, Anatoliy N. Tyulpakov

    Diterbitkan 2019-08-01
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  5. 5
    Study of molecular basis of thyroid dysgenesis

    Study of molecular basis of thyroid dysgenesis oleh Nina A. Makretskaya, Olga B. Bezlepkina, Anna A. Kolodkina, Alexey V. Kiyaev, Evgeny V. Vasilyev, Vasily M. Petrov, Olga A. Chikulaeva, Oleg A. Malievsky, Ivan I. Dedov, Anatoliy N. Tyulpakov

    Diterbitkan 2018-08-01
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