Effectiveness of multidisciplinary team as a new model of after stroke patients’ rehabilitation

Ivanova, G., Melnikova, E., Shmonin, A., Verbitskaya, E., Belkin, A., Bodrova, R., Lebedev, P., Maltseva, M., Prokopenko, S., Prosvirnina, M., Sarana, A., Stakhovskaya, L., Suvorov, A., Khasanova, D. & Shamalov, N., 31 Dec 2019, In: Bulletin of Russian State Medical University. 2019;6, p. 5-14

Research output: Contribution to journal › Article › peer-review

Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes

Glotov, O. S., Serebryakova, E. A., Turkunova, M. E., Efimova, O. A., Glotov, A. S., Barbitoff, Y. A., Nasykhova, Y. A., Predeus, A. V., Polev, D. E., Fedyakov, M. A., Polyakova, I. V., Ivashchenko, T. E., Shved, N. Y., Shabanova, E. S., Tiselko, A. V., Romanova, O. V., Sarana, A. M., Pendina, A. A., Scherbak, S. G., Musina, E. V. & 10 others, Petrovskaia-Kaminskaia, A. V., Lonishin, L. R., Ditkovskaya, L. V., Zhelenina, L. А., Tyrtova, L. V., Berseneva, O. S., Skitchenko, R. K., Suspitsin, E. N., Bashnina, E. B. & Baranov, V. S., Dec 2019, In: Molecular Medicine Reports. 20, 6, p. 4905-4914 10 p.

Research output: Contribution to journal › Article › peer-review

Reproductive History of a Woman With 8p and 18p Genetic Imbalance and Minor Phenotypic Abnormalities

Pendina, A. A., Shilenkova, Y. V., Talantova, O. E., Efimova, O. A., Chiryaeva, O. G., Malysheva, O. V., Dudkina, V. S., Petrova, L. I., Serebryakova, E. A., Shabanova, E. S., Mekina, I. D., Komarova, E. M., Koltsova, A. S., Tikhonov, A. V., Tral, T. G., Tolibova, G. K., Osinovskaya, N. S., Krapivin, M. I., Petrovskaia-Kaminskaia, A. V., Korchak, T. S. & 16 others, Ivashchenko, T. E., Glotov, O. S., Romanova, O. V., Shikov, A. E., Urazov, S. P., Tsay, V. V., Eismont, Y. A., Scherbak, S. G., Sagurova, Y. M., Vashukova, E. S., Kozyulina, P. Y., Dvoynova, N. M., Glotov, A. S., Baranov, V. S., Gzgzyan, A. M. & Kogan, I. Y., 20 Nov 2019, In: Frontiers in Genetics. 10, 1164.

Research output: Contribution to journal › Article › peer-review

CT-fusion-guided endovascular repair of iatrogenic common iliac artery aneurysm: A case report

Khilchuk, A., Vlasenko, S., Muradyan, M., Agarkov, M., Abdulkarim, D., Shcherbak, S., Gladyshev, D., Sarana, A., Litvinovskii, S. & Kovalik, V., Nov 2019, In: Radiology Case Reports. 14, 11, p. 1394-1400 7 p.

Research output: Contribution to journal › Article › peer-review

Endovascular management of the peripherally inserted central venous catheter iatrogenic pinch-off syndrome: A case report

Vlasenko, S. V., Agarkov, M. V., Khilchuk, A. A., Scherbak, S. G., Sarana, A. M., Karmazanashvili, E. G., Kalinina, L. P. & Volkov, V. G., 1 Mar 2019, In: Radiology Case Reports. 14, 3, p. 381-384 4 p.

Research output: Contribution to journal › Article › peer-review

БИОМАРКЕРЫ КОНТРАСТ-ИНДУЦИРОВАННОГО ОСТРОГО ПОЧЕЧНОГО ПОВРЕЖДЕНИЯ ПОСЛЕ ЧРЕСКОЖНЫХ КОРОНАРНЫХ ВМЕШАТЕЛЬСТВ

Хильчук, А. А., Абугов, С. А., Власенко, С. В., Щербак, С. Г., Сарана, А. М., Агарков, М. В. & Кармазанашвили, Е. Г., Mar 2019, In: НЕФРОЛОГИЯ И ДИАЛИЗ. 21, 3, p. 301-311

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New Frameshift Mutation Found in NEW PKP2 Gene in Arrhythmogenic Right Ventricular Cardiomiopathy/Displasia a Family Case Study

Fedyakov, M. A., Veleslavova, O. E., Romanova, O. V., Shubik, Y. V., Urazov, S. P., Rud, S. D., Сарана, А. М., Щербак, С. Г. & Глотов, О. С., 2019, In: Вестник Санкт-Петербургского государственного университета. Серия 11. Медицина. 14, 1, p. 5–21

Research output: Contribution to journal › Article › peer-review

New frameshift mutation found in PKP2 gene in arhythmogenic right ventricular cardiomyopathy/dysplasia:a family case study.

Fedyakov, M. A., Veleslavova, O. E., Romanova, O. V., Shubik, Y. V., Urazov, S. P., Rud, S. D., Sarana, A. M., Scherbak, S. G. & Glotov, O. S., 2019, In: Вестник Санкт-Петербургского университета. Медицина. 14, 1, p. 3-13

Research output: Contribution to journal › Article