The Integrative Approach to Study of the Structure and Functions of Cardiac Voltage-Dependent Ion Channels by Kacher, Y. G., Karlova, M. G., Glukhov, G. S., Zhang, H., Zaklyazminskaya, E. V., Loussouarn, G., Sokolova, O. S.

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Phenotypic Manifestations of Val93Ile Missense Mutation and Its Influence on Kir2.1 Channel Functioning by Zhang, H., Glukhov, G. S., Pustovit, K. B., Kacher, Yu. G., Rusinova, V. S., Kiseleva, I. I., Komolyatova, V. N., Makarov, L. M., Zaklyazminskaya, E. V., Sokolova, O. S.

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Laminopathies in Russian families by Rudenskaya, GE, Polyakov, AV, Tverskaya, SM, Zaklyazminskaya, EV, Chukhrova, AL, Groznova, OE, Ginter, EK

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Noncompact myocardium with dilated phenotype: differences in comparison with other forms of dilated cardiomyopathy by Blagova, O, Pavlenko, E V, Varionchik, N V, Sedov, V P, Polyak, M E, Zaklyazminskaya, E V

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Combination of arrhythmogenic right ventricular dysplasia with left ventricular non-compaction as a special form of cardiomyopathy: clinic, diagnostics, genetic, natural course by Lutokhina, Y A, Blagova, O V, Shestak, A G, Polyak, M E, Bukaeva, A A, Zaklyazminskaya, E V, Varionchik, N V, Sedov, V P, Kogan, E A, Alexandrova, S A, Nedostup, A V

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Myocardial Biopsy In "Idiopathic» Atrial Fibrillation And Other Arrhythmias: Nosological Diagnosis, Clinical And Morphological Parallels, And Treatment by Blagova, O V, Nedostup, A V, Kogan, E A, Sulimov, V A, Abugov, S A, Kupriyanova, A G, Zaydenov, V A, Donnikov, A E, Zaklyazminskaya, E V, Okisheva, E A

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Laminopathies in Russian families by RUDENSKAYA, G. E, POLYAKOV, A. V, TVERSKAYA, S. M, ZAKLYAZMINSKAYA, E. V, CHUKHROVA, A. L, GROZNOVA, O. E, GINTER, E. K

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New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling by Polyak, Margarita E, Zaklyazminskaya, Elena V

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De Novo Asp219Val Mutation in Cardiac Tropomyosin Associated with Hypertrophic Cardiomyopathy by Tsaturyan, Andrey K, Zaklyazminskaya, Elena V, Polyak, Margarita E, Kopylova, Galina V, Shchepkin, Daniil V, Kochurova, Anastasia M, Gonchar, Anastasiia D, Kleymenov, Sergey Y, Koubasova, Natalia A, Bershitsky, Sergey Y, Matyushenko, Alexander M, Levitsky, Dmitrii I

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Biallelic variants in PPP1R13L cause paediatric dilated cardiomyopathy by Robinson, H.K., Zaklyazminskaya, E., Povolotskaya, I., Surikova, Y., Mallin, L., Armstrong, C., Mabin, D., Benke, P.J., Chrisant, M.R., McDonald, M., Marboe, C.C., Agre, K.E., Deyle, D.R., McWalter, K., Douglas, G., Balashova, M.S., Kaimonov, V., Shirokova, N., Pomerantseva, E., Turner, C.L., Ellard, S.

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New Recessive Dystrophic Epidermolysis Bullosa intermediate variant resulting from alternative splicing of exon 19 and truncation in FN III-like domain of type VII collagen by Martynova, Aleksandra A, Kubanov, Alexey A, Evtushenko, Nadezhda A, Kosykh, Anastasiya V, Kondratyev, Nikolay V, Beilin, Arkadii K, Karamova, Arfenya E, Monchakovskaya, Ekaterina S, Bogdanova, Ekaterina A, Azimov, Karim A, Ziganshin, Rustam H, Nefedova, Maria A, Bozhanova, Nina G, Zaklyazminskaya, Elena V, Gurskaya, Nadya G

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