Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D V Bryunin"'
Autor:
N A Arutyunyan, T A Dzhibladze, V M Zuev, A I Ishchenko, D V Bryunin, I D Hohlova, I V Gadaeva, A A Siordiya
Publikováno v:
Гинекология, Vol 17, Iss 3, Pp 93-96 (2015)
In the article information is resulted about the complex inspection of women with fruitlessness and different endometrial pathology, including the immunogistokhimicheskie methods of diagnostics. 100 patients are inspected in age from 27 to 42 years,
Externí odkaz:
https://doaj.org/article/6df6244aa9634bb6aed19550cfe442c1
Autor:
D V Bryunin
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss S7, Pp 57-58 (2012)
Externí odkaz:
https://doaj.org/article/f1acc50140f640e6b4d525de3ac93151
Autor:
D V Bryunin
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss S7, Pp 56-57 (2012)
Externí odkaz:
https://doaj.org/article/49bd8a065a5f4aaea24dbc3a941d3f1c
Publikováno v:
RUDN Journal of Medicine, Vol 0, Iss S7, Pp 189-190 (2012)
Externí odkaz:
https://doaj.org/article/f7af8ece715f4fa98422286ca53e9ec0
Autor:
E. A. Dubova, К. A. Pavlov, S. V. Lishchuk, A. S. Tertychnyi, A. A. Bakhvalova, D. V. Bryunin
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 46, Iss 4, Pp 374-378 (2018)
Wolffian tumor is a rare neoplasm arising from mesonephric duct remnants. Not more than 100 cases of the disease have been described. The authors present their own clinical observation of the Wolffian tumor in a 43-year old female patient. Radiologic
Externí odkaz:
https://doaj.org/article/3e890d2b320f44a39f96a9f6179727d6
Publikováno v:
Urologiia (Moscow, Russia : 1999). (4)
The article is focused on the problem of diagnosis and surgical treatment of infiltrative forms of endometriosis with lesions of both internal genitalia and urinary tract. A clinical observation of a young woman who underwent a robot-assisted operati
Autor:
A. S. Tertychnyi, A. A. Bakhvalova, E. A. Dubova, S. V. Lishchuk, К. A. Pavlov, D. V. Bryunin
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 46, Iss 4, Pp 374-378 (2018)
Wolffian tumor is a rare neoplasm arising from mesonephric duct remnants. Not more than 100 cases of the disease have been described. The authors present their own clinical observation of the Wolffian tumor in a 43-year old female patient. Radiologic
Autor:
M F, Kalashnikova, N V, Likhodey, A N, Tiulpakov, E V, Fedorova, D V, Bryunin, A A, Bakhvalova, M A, Glushakova, S A, Smirnova, V V, Fadeyev
Publikováno v:
Problemy endokrinologii. 65(4)
SertoliLeydig cell tumor is a rather rare type of ovarian neoplasms belonging to the group of sex cordstromal tumors. This malignancy is characterized by androgen overproduction, which results in the so-called virilization and can be accompanied by v