The use of chromosomal microarray analysis for diagnostics of chromosomal pathology in fetal central nervous system malformations
Kievskaya, J. K., Kanivets, I. V., Kudryavtseva, E. V., Pyankov, D. V., Korostelev, S. A.
Published in Акушерство, гинекология и репродукция (14.10.2020)
Published in Акушерство, гинекология и репродукция (14.10.2020)
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SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold
Kievskaya, J K, Shilova, N V, Kanivets, I V, Kudryavtseva, E V, Pyankov, D V, Korostelev, S A
Published in Sovremennye tekhnologii v medit͡s︡ine (01.01.2021)
Published in Sovremennye tekhnologii v medit͡s︡ine (01.01.2021)
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Glutaric aciduria type 1 in children. Clinical presentation of 46 cases in Russian families
Mikhailova, S. V., Saifullina, E. V., Baranova, P. V., Vorontsova, V. P. , Gribov, D. I. , Zhivihina, M. V., Slatetskaya, A. N. , Magzhanov, R. V. , Samokhvalov, V. A. , Virtseva, M. N., Borscheva, L. P., Koh, E. E., Novikova, M. V., Abrukova, A. V. , Belyashova, E. Yu, Gerasimenko, N. Yu, Guseva, L. V., Yukhimenko, Zh. V., Nikitina, N. V., Belyaeva, T. I. , Shkurko, T. A., Pichkur, N. A., Kakaulina, V. S., Pechatnikova, N. L., Polyakova, N . A., Korostelev, S. A., Pyankov, D. V., Kanivets, I. V., Demina, N. A., Pyrkova, E. Yu, Baidakova, G. V., Kurkina, M. V., Zakharova, E. Yu
Published in Nervno-myshechnye bolezni (13.09.2021)
Published in Nervno-myshechnye bolezni (13.09.2021)
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Epidemiologic, clinical and pathogenesis features of achromatopsia in the Russian population
Ivanova, M. E., Zolnikova, I. V., Khatsenko, I. E., Strelnikov, V. V., Konovalov, F. A., Lozier, E. R., Ampleeva, M. A., Antonets, A. V., Kanivets, I. V., Gorgisheli, K. V., Atarshchikov, D. S., Pyankov, D. V., Korostelev, S. A., Kuznetsova, E. B., Bar, D., Balashova, L. M., Salmasi, Zh. M.
Published in Rossiĭskiĭ oftalʹmologicheskiĭ zhurnal (15.03.2020)
Published in Rossiĭskiĭ oftalʹmologicheskiĭ zhurnal (15.03.2020)
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BRAF-positive paucicellular variant of anaplastic carcinoma in the presence of tall cell variant papillary thyroid cancer
Dolzhansky, O V, Paltseva, E M, Khmelkova, D N, Konovalov, F A, Kanivets, I V, Lavrov, A V, Pyankov, D V, Korostelev, S A, Levendyuk, O A, Pominalnaya, V M, Fedorov, D N
Published in Arkhiv patologii (2017)
Published in Arkhiv patologii (2017)
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Glutaric aciduria type 1 in children. Clinical presentation of 46 cases in Russian families
Mikhailova, S V, Saifullina, E V, Baranova, P V, Vorontsova, V P, Gribov, D I, Zhivihina, M V, Slatetskaya, A N, Magzhanov, R V, Samokhvalov, V A, Virtseva, M N, Borscheva, L P, Koh, E E, Novikova, M V, Abrukova, A V, E. Yu. Belyashova, N. Yu. Gerasimenko, Guseva, L V, Yukhimenko, Zh V, Nikitina, N V, Belyaeva, T I, Shkurko, T A, Pichkur, N A, Kakaulina, V S, Pechatnikova, N L, N . A. Polyakova, Korostelev, S A, Pyankov, D V, Kanivets, I V, Demina, N A, E. Yu. Pyrkova, Baidakova, G V, Kurkina, M V, E. Yu. Zakharova
Published in Nervno-myshechnye bolezni (01.01.2021)
Published in Nervno-myshechnye bolezni (01.01.2021)
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Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy
Vasilyeva, T A, Kadyshev, V V, Marakhonov, A V, Kanivets, I V, Korostelev, S A, Koshkin, P A, Pyankov, D V, Petrova, N V, Kutsev, S I, Zinchenko, R A
Published in Vestnik oftal'mologii (2023)
Published in Vestnik oftal'mologii (2023)
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