Zobrazeno 1 - 10
of 79
pro vyhledávání: '"V.V. Kadyshev"'
Autor:
N.V. Sukhanova, V.V. Kadyshev, T.A. Vasilieva, A.V. Marakhonov, L.A. Katargina, S.I. Kutsev, R.A. Zinchenko
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 23, Iss 1 (2023)
N.V. Sukhanova1, V.V. Kadyshev1, T.A. Vasilieva1, A.V. Marakhonov1, L.A. Katargina 2, S.I. Kutsev1, R.A. Zinchenko1,3 1Research Center for Medical Genetics, Moscow, Russian Federation 2Helmholtz National Medical Research Center for Eye Diseases
Externí odkaz:
https://doaj.org/article/5ebe4119cfe94260a1b985b950813271
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 22, Iss 2 (2022)
V.V. Kadyshev1, E.K. Ginter1, S.I. Kutsev1, Zh.G. Oganezova1,2, R.A. Zinchenko1,3 1Research Center for Medical Genetics, Moscow, Russian Federation 2Pirogov Russian National Research Medical University, Moscow, Russian Federation 3N.A. Semas
Externí odkaz:
https://doaj.org/article/233713ed987c4084b88abf0a5046641d
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 21, Iss 3 (2021)
V.V. Kadyshev, S.A. Ryazhskaya, O.V. Khalanskaya, N.V. Zhurkova, R.A. Zinchenko Research Center for Medical Genetics, Moscow, Russian Federation Albinism is a clinically and genetically heterogeneous group of hereditary diseases whose pathogene
Externí odkaz:
https://doaj.org/article/fff75fe79ab540bcb46038bda9a4561c
Autor:
M.E. Ivanova, V.V. Kadyshev, D.S. Atarshchikov, I.V. Zolnikova, N.P. Akchurina, N.K. Serova, F.A. Konovalov, E.R. Lozier, E.A. Pomerantseva, N.V. Vetrova, D. Barh, L.M. Balashova, J.M. Salmasi
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 20, Iss 1 (2020)
M.E. Ivanova1, V.V. Kadyshev2, D.S. Atarshchikov3, I.V. Zolnikova4, N.P. Akchurina4, N.K. Serova5, F.A. Konovalov6, E.R. Lozier6, E.A. Pomerantseva7, N.V. Vetrova7, D. Barh8, L.M. Balashova9, J.M. Salmasi10 1 LLC “Oftalmic”, Moscow, Russian Fe
Externí odkaz:
https://doaj.org/article/ef25af0d1df74af28e7306ba9626c3cc
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 19, Iss 4 (2019)
M. Kh. Khubetsova1, V.V. Kadyshev2, B.F. Ambalova3 1S.N. Fedorov NMRC “MNTK “Eye Microsurgery”, Moscow, Russian Federation 2Moscow Genetic Research Center, Moscow, Russian Federation 3Right-Shore Central Regional Clinical Hospital, Bes
Externí odkaz:
https://doaj.org/article/2394e03d3f22442a96692c2efcbb6786
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 19, Iss 1 (2019)
V.V. Kadyshev1, A.V. Marakhonov1, S.I. Kutsev1,2, R.A. Zinchenko1,3 1 Research Centre of Medical Genetics of the Russian Academy of Medical Sciences, Moscow, Russian Federation 2 Pirogov Russian National Research Medical University, Moscow, Russi
Externí odkaz:
https://doaj.org/article/4fd41fb4b662420b9c0905135637a7d8
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 18, Iss 3 (2018)
V.V. Kadyshev1, A.V. Marakhonov1, S.I. Kutsev1,2, R.A. Zinchenko1,3 1 Research Centre of Medical Genetics of the Russian Academy of Medical Sciences, Moscow, Russian Federation 2 Pirogov Russian National Research Medical University, Moscow, Russian
Externí odkaz:
https://doaj.org/article/5c98419cbdb943a9b0068dd588c6e739
Autor:
T.A. Vasilieva, Voskresenskaya A. A, V.V. Kadyshev, N.A. Pozdeeva, A.V. Marakhonov, R.A. Zinchenko
Publikováno v:
РМЖ "Клиническая офтальмология", Vol 18, Iss 1 (2018)
Vasilyeva T. A.1, Voskresenskaya A. A.2, Kadyshev V. V.1, Pozdeyeva N. A.2, Marakhonov A. V.1,3, Zinchenko R. A.1,4 1 Research Center for Medical Genetics, Moscow 2 Cheboksary branch of S. Fyodorov Eye Microsurgery Federal State Institution 3 Mosc
Externí odkaz:
https://doaj.org/article/d6d85eef0a184e709f9bace000cc2b66
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
[Gyrate atrophy of the choroid and retina with ornithinemia and foveoschisis (clinical observation)]
Autor:
I.V. Zolnikova, S.V. Milash, R.A. Zinchenko, A.V. Polyakov, A.A. Stepanova, A.B. Chernyak, A.A. Sianosyan, I.V. Egorova, V.V. Kadyshev
Publikováno v:
Vestnik oftalmologii. 138(5)
Gyrate chorioretinal atrophy (GCA) is a rare hereditary disease with certain complications; one extremely rare complication of GCA is foveoschisis. For the first time in Russian ophthalmology, a 10-year-old female child has been described to have gen