Showing 1 - 6 results of 6 for search 'T. A. Pomerantseva', query time: 0.03s Refine Results
  1. 1
    THE MAIN COMPONENTS OF SOCIALIZATION AND INDIVIDUALIZATION OF PRIMARY SCHOOL CHILDREN

    THE MAIN COMPONENTS OF SOCIALIZATION AND INDIVIDUALIZATION OF PRIMARY SCHOOL CHILDREN by T. A. Pomerantseva

    Published 2018-11-01
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  2. 2
    Clinical and genetic characteristics of the early 66th type epileptic encephalopathy (literature review and own observation)

    Clinical and genetic characteristics of the early 66th type epileptic encephalopathy (literature review and own observation) by T. V. Markova, A. O. Borovikov, E. R. Lozier, A. A. Isaev, V. S. Kaimonov, E. A. Pomerantseva, F. A. Konovalov, O. A. Schagina, E. L. Dadali

    Published 2020-06-01
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  3. 3
    A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing

    A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing by Ekaterina A. Gibitova, Pavel V. Dobrynin, Ekaterina A. Pomerantseva, Elizaveta V. Musatova, Anna Kostareva, Igor Evsyukov, Sergey Y. Rychkov, Olga V. Zhukova, Oxana Y. Naumova, Elena L. Grigorenko

    Published 2022-05-01
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  4. 4
    Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia))

    Case of phenotype of optic nerve atrophy due to mutation in С19orf12 gene (neurodegeneration with the brain iron accumulation (nbia)) by M.E. Ivanova, V.V. Kadyshev, D.S. Atarshchikov, I.V. Zolnikova, N.P. Akchurina, N.K. Serova, F.A. Konovalov, E.R. Lozier, E.A. Pomerantseva, N.V. Vetrova, D. Barh, L.M. Balashova, J.M. Salmasi

    Published 2020-03-01
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  5. 5
    Corrigendum to “Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene” [59 (2022) 102648]

    Corrigendum to “Generation of two iPSC lines from healthy donor with a heterozygous mutation in the VPS13B gene” [59 (2022) 102648] by S.A. Chechetkina, A.A. Khabarova, A.S Chvileva, O.M. Kurchenko, A.V. Smirnov, A.M. Yunusova, I.N. Kotov, E.V. Musatova, E.A. Pomerantseva, E.A. Volovikov, M.A. Lagarkova, T.A. Shnaider, I.E. Pristyazhnyuk

    Published 2022-07-01
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  6. 6
    Ultrastructural Abnormalities in Induced Pluripotent Stem Cell-Derived Neural Stem Cells and Neurons of Two Cohen Syndrome Patients

    Ultrastructural Abnormalities in Induced Pluripotent Stem Cell-Derived Neural Stem Cells and Neurons of Two Cohen Syndrome Patients by Tatiana A. Shnaider, Anna A. Khabarova, Ksenia N. Morozova, Anastasia M. Yunusova, Sophia A. Yakovleva, Anastasia S. Chvileva, Ekaterina R. Wolf, Elena V. Kiseleva, Elena V. Grigor’eva, Viktori Y. Voinova, Maria A. Lagarkova, Ekaterina A. Pomerantseva, Elizaveta V. Musatova, Alexander V. Smirnov, Anna V. Smirnova, Diana S. Stoklitskaya, Tatiana I. Arefieva, Daria A. Larina, Tatiana V. Nikitina, Inna E. Pristyazhnyuk

    Published 2023-11-01
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