Works matching AU Nikolaeva, Ekaterina A.


Results: 19
    1

    Neuronal ceroid lipofuscinosis in the Russian population: Two novel mutations and the prevalence of heterozygous carriers.

    Published in:
    Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 7, p. 1, doi. 10.1002/mgg3.1228
    By:
    • Kozina, Anastasiya A.;
    • Okuneva, Elena G.;
    • Baryshnikova, Natalia V.;
    • Kondakova, Olga B.;
    • Nikolaeva, Ekaterina A.;
    • Fedoniuk, Inessa D.;
    • Mikhailova, Svetlana V.;
    • Krasnenko, Anna Y.;
    • Stetsenko, Ivan F.;
    • Plotnikov, Nikolay A.;
    • Klimchuk, Olesia I.;
    • Popov, Yaroslav V.;
    • Surkova, Ekaterina I.;
    • Shatalov, Peter A.;
    • Rakitko, Alexander S.;
    • Ilinsky, Valery V.
    Publication type:
    Article
    2
    3
    4
    5
    6
    7
    8
    9

    Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.

    Published in:
    International Journal of Molecular Sciences, 2023, v. 24, n. 2, p. 1597, doi. 10.3390/ijms24021597
    By:
    • Kistol, Denis;
    • Tsygankova, Polina;
    • Krylova, Tatiana;
    • Bychkov, Igor;
    • Itkis, Yulia;
    • Nikolaeva, Ekaterina;
    • Mikhailova, Svetlana;
    • Sumina, Maria;
    • Pechatnikova, Natalia;
    • Kurbatov, Sergey;
    • Bostanova, Fatima;
    • Migiaev, Ochir;
    • Zakharova, Ekaterina
    Publication type:
    Article
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19