Hasil Pencarian - Elena V. Shakhtshneider

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  1. 1
    Molecular genetic diagnosis of a heterozygous form of familial hypercholesterolemia at a young age: a clinical case

    Molecular genetic diagnosis of a heterozygous form of familial hypercholesterolemia at a young age: a clinical case oleh Olga V. Timoshchenko, Dinara E. Ivanoshchuk, Sergey E. Semaev, Lyudmila D. Latyntseva, Elena V. Shakhtshneider

    Diterbitkan 2022-04-01
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  2. 2
    Diabetes mellitus associated with the mutation of the ABCC8 gene (MODY 12): features of clinical course and therapy

    Diabetes mellitus associated with the mutation of the ABCC8 gene (MODY 12): features of clinical course and therapy oleh Alla K. Ovsyannikova, Oksana D. Rymar, Elena V. Shakhtshneider, Vadim V. Klimontov, Elena A. Koroleva, Mikhail I. Voevoda

    Diterbitkan 2019-03-01
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  3. 3
    Variants of the HNF4A and HNF1A genes in patients with impaired glucose metabolism and dyslipidemia

    Variants of the HNF4A and HNF1A genes in patients with impaired glucose metabolism and dyslipidemia oleh Dinara E. Ivanoshchuk, Alla K. Ovsyannikova, Svetlana V. Mikhailova, Elena V. Shakhtshneider, Emil S. Valeev, Oksana D. Rymar, Pavel S. Orlov, Mikhail I. Voevoda

    Diterbitkan 2022-01-01
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