Liver venous deprivation in the prevention of post-resection hepatic failure von Sudakov, M. A., Shchekoturov, I. O., Vasilenko, E. I., Cholak, P. M., Emelyanova, A. S., Savostyanov, K. A., Egorov, A. V., Vetshev, F. P.

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Clinical and Genetic Characteristics of Pediatric Patients with Hypophosphatasia in the Russian Population von Glotov, Oleg S, Savostyanov, Kirill V, Nagornova, Tatyana S, Chernov, Alexandr N, Fedyakov, Mikhail A, Raspopova, Aleksandra N, Krasnoukhov, Konstantin N, Danilov, Lavrentii G, Moiseeva, Nadegda V, Kalinin, Roman S, Tsai, Victoria V, Eismont, Yuri A, Voinova, Victoria Y, Vitebskaya, Alisa V, Gurkina, Elena Y, Kuzenkova, Ludmila M, Sosnina, Irina B, Pushkov, Alexander A, Zhanin, Ilya S, Zakharova, Ekaterina Y

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The prevalence of Fabry disease among 1009 unrelated patients with hypertrophic cardiomyopathy: a Russian nationwide screening program using NGS technology von Savostyanov, K, Pushkov, A, Zhanin, I, Mazanova, N, Trufanov, S, Pakhomov, A, Alexeeva, A, Sladkov, D, Asanov, A, Fisenko, A

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Signatures of Dermal Fibroblasts from RDEB Pediatric Patients von Beilin, Arkadii K., Evtushenko, Nadezhda A., Lukyanov, Daniil K., Murashkin, Nikolay N., Ambarchian, Eduard T., Pushkov, Alexander A., Savostyanov, Kirill V., Fisenko, Andrey P., Rogovaya, Olga S., Vasiliev, Andrey V., Vorotelyak, Ekaterina A., Gurskaya, Nadya G.

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P069 Experience in the use of elexacaftor/tezacaftor/ivacaftor in cystic fibrosis patients of the Chechen ethnic group in the Russian Federation von Simonov, M., Gorinova, Y., Simonova, O., Savostyanov, K., Pushkov, A.

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Neuroprotective and anti-inflammatory properties of proteins secreted by glial progenitor cells derived from human iPSCs von Salikhova, Diana I, Shedenkova, Margarita O, Sudina, Anastasya K, Belousova, Ekaterina V, Krasilnikova, Irina A, Nekrasova, Anastasya A, Nefedova, Zlata A, Frolov, Daniil A, Fatkhudinov, Timur Kh, Makarov, Andrey V, Surin, Alexander M, Savostyanov, Kirill V, Goldshtein, Dmitry V, Bakaeva, Zanda V

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Bavaria's external relations von Minkova, K. V., Savostyanov, A. A.

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Genetic Landscape of Nephropathic Cystinosis in Russian Children von Savostyanov, K V, Pushkov, A A, Shchagina, O A, Maltseva, V V, Suleymanov, E A, Zhanin, I S, Mazanova, N N, Fisenko, A P, Mishakova, P S, Polyakov, A V, Balanovska, E V, Zinchenko, R A, Tsygin, A N

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Multiple coronary fistulae into left ventricle as a rare cause of myocardial ischemia von Averkova, A, Savostyanov, K, Zateyshchikov, D

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338 Features of genotype-phenotype correlation in siblings with cystic fibrosis von Simonov, M., Krasnovidova, A., Simonova, O., Gorinova, Y., Chernevich, V., Savostyanov, K., Pushkov, A.

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P030 Features of clinical course of cystic fibrosis in patients from Chechen Republic von Simonov, M., Gorinova, Y., Simonova, O., Savostyanov, K., Pushkov, A., Alekseeva, A.

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308 The new cell cultures from dystrophic epidermolysis bullosa patients in Russia von Beilin, A., Evtushenko, N., Murashkin, N., Savostyanov, K., Fisenko, A., Ambarchyan, E., Vorotelyak, E., Gurskaya, N.

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P001 Phenotypic features of cystic fibrosis gene mutations in patients from the Russian Federation von Gorinova, Y., Savostyanov, K., Pushkov, A., Krasovskiy, S., Simonova, O.

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111 Next generation sequencing is the suitable method for identification of hereditary dermatosis with EB symptom complex in Russian patients von Pushkov, A., Murashkin, N., Fisenko, A., Trufanov, S., Nikitin, A., Pakhomov, A., Sladkov, D., Ambarchyan, E., Savostyanov, K.

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Delayed motor, mental and speech development and congenital brain malformations: the first description of Zhu–Tokita–Takenouchi–Kim syndrome in Russia von Kondakova, O. B., Gudkova, A. P., Demyanov, S. V., Davydova, Yu. I., Lyalina, A. A., Grebenkin, D. I., Bakovich, E. A., Kanivets, I. V., Demyanov, D. S., Zhanin, I. S., Pushkov, A. A., Savostyanov, K. V.

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Family case of aromatic L-amino acid decarboxylase deficiency von Kondakova, O. B., Kazakova, K. A., Lyalina, A. A., Lapshina, N. V., Pushkov, A. A., Mazanova, N. N., Davydova, Yu. I., Grebenkin, D. I., Kanivets, I. V., Savostyanov, K. V.

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Prospects of etiopathogenetic treatment of Huntington’s disease von Kondakova, O. B., Demyanov, S. V., Krasivskaya, A. V., Demyanov, G. V., Grebenkin, D. I., Davydova, Yu. I., Lyalina, A. A., Radkevich, E. R., Savostyanov, K. V.

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AB0863 High Frequency of Caps and Traps in Russian Patients with Systemic Juvenile Idiopathic Arthritis von Alexeeva, E., Savostyanov, K., Sleptsova, T., Pushkov, A., Bzarova, T., Valieva, S., Denisova, R., Isayeva, K., Chistyakova, E., Lomakina, O., Soloshenko, M., Kaschenko, E.

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Molecular genetic features of the development of restrictive cardiomyopathy in Russian children von Savostyanov, K. V., Basargina, E. N., Ryabova, E. E., Pushkov, A. A., Zhanin, I. S., Basargina, E. Yu, Alekseeva, A. Yu, Muraveva, L. V., Gandaeva, L. A., Fisenko, A. P.

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AB0888 Mutations in TNFRSF1A and NLRP3 Genes in Patients with Recurrent Inflammatory Attacks in Russian Population von Savostyanov, K., Alexeeva, E., Sleptsova, T., Pushkov, A., Valieva, S., Bzarova, T., Denisova, R., Mitenko, E., Nikitin, A., Isayeva, K., Chomahidze, A., Fetisova, A., Chistyakova, E.

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