Determination of frequencies of alleles, associated with the pseudodeficiency of lysosomal hydrolases, in population of Ukraine by Olkhovych, N V, Gorovenko, N G

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Major mutation p.His281Tyr in Gene GLB1 in patients with GM1-gangliosidosis in Ukraine by Mytsyk, N. Y., Olkhovych, N. V., Gorovenko, N. G.

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Spectrum of mutations in patients with organic acidurias from Ukraine by Barvinska, O. I., Olkhovych, N. V., Shkurko, T. O., Gorovenko, N. G.

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Variation in particular biochemical indicators, cytokine and adipokine profiles of the blood, and the structural and functional parameters of the liver in patients with nonalcoholic fatty liver disease and different genotypes by the polymorphic locus A313G of the GSTP1 gene by Prysyazhnyuk, V. P., Rossokha, Z. I., Gorovenko, N. G.

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Molecular-genetic characterization of Ukrainian patients with mucopolysaccharidosis IIIA: identification of three new mutations in the heparan-N-sulfatase gene by Trofimova, N. S., Olkhovich, N. V., Gorovenko, N. G.

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Identification and characterization of six new mutations in GLB1 gene in Ukrainian patients with GM1 gangliosidosis and Morquio B disease by Mytsyk, N. Y., Gorovenko, N. G.

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Specificities of Sanfilippo A syndrome laboratory diagnostics by Trofimova, N. S., Olkhovich, N. V., Gorovenko, N. G.

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DIFFERENTIATION OF NORM AND PATHOLOGY DURING SELECTIVE BIOCHEMICAL SKREENING OF LYSOSOMAL STORAGE DISEASES WITH INCREASED EXCRETION OF OLIGOSACCHARIDES by Mytsyk, N Y, Olkhovych, N V, Gorovenko, N G

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The frequency of alleles in the GSTT1 and GSTM1 genes involved in phase II of xenobiotic transformation in long-lived people of subcarpathia by Kozovyi, R. V., Podolska, S. V., Gorovenko, N. G.

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role of genetic determinant in the development of severe perinatal asphyxia by Gorovenko, N. G, Rossokha, Z. I, Podolskaya, S. V, Pokhylko, V. I, Lundberg, G. A

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Early detection and group-specific identification of Mycobacterium tuberculosis strains by method of single-nucleotide polymorphism analysis with hairpin primers by Cherednyk, Yu. O., Anopryenko, O. V., Gorovenko, N. G., Feschenko, Yu. I.

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Study on association of the polymorphic variants of ACE (I/D), AT2R1 (A1166C), TNF-α (G308A), MTHFR (C677T) genes and their combinations with the risk of development of perinatal pathology and gestation reduction by Gorovenko, N. G., Kyryachenko, S. P., Rossokha, Z. I.

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Comparative evaluation of genetic risk models of reproductive disorders caused by MTHFR, MTRR, MTR1 gene polymorphism by Rossokha, Z. І., Kyriachenko, S. P., Gorovenko, N. G.

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Pharmacogenetic substantiation of personalized prescription of oral anticoagulants in clinical practice by Bentsionova, K I, Rossokha, Z I, Ievseienkova, O G, Gorovenko, N G

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Efficiency of application of different DNA probes in identifying marker chromosomes by Tavokina, L. V., Brovko, A. O., Baronova, E. V., Moskalenko, E. P., Gorovenko, N. G.

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Identification of the nonsense mutation W1282X in two cystic fibrosis families from Ukraine by Gusak, N. M., Gorovenko, N. G., Buzhievskaya, T. I.

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Determining the frequency of common mutations in the GBA gene in patients with Gaucher disease in Ukraine by Gorovenko, N. G., Ol’khovich, N. V., Nedoboy, A. M., Pichkur, N. O.

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Pharmacogenetic substantiation of personalized prescription of oral anticoagulants in clinical practice by Bentsionova, K.I., Rossokha, Z.I., Ievseienkova, O.G., Gorovenko, N.G.

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Comparative evaluation of genetic risk models of reproductive disorders caused by MTHFR, MTRR, MTR1 gene polymorphism by Rossokha, Z І, Kyriachenko, S P, Gorovenko, N G

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Leiden mutation (rs6025) in a severe COVID-19 pneumonia patient with Down syndrome: a clinical case by Pokhylko, V.I., Cherniavska, Y.I., Fishchuk, L.Y., Rossokha, Z.I., Ievseienkova, O.G., Dubitska, O.M., Popova, O.F., Fastovets, M.М., Kaliuzhka, O.О., Gorovenko, N.G.

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