Zobrazeno 1 - 10
of 171
pro vyhledávání: '"N S Kuznetsov"'
Publikováno v:
Эндокринная хирургия, Vol 9, Iss 2, Pp 31-35 (2015)
One of the most difficult in diagnostic and treatment options for endogenous Cushing is the ectopic ACTH syndrome, which causes the development of tumors of different histogenesis localization producing adrenocorticotropic hormone (ACTH), and much le
Externí odkaz:
https://doaj.org/article/1ad516e92967445697dd25a1fd4c188f
Publikováno v:
Эндокринная хирургия, Vol 8, Iss 2, Pp 4-8 (2014)
Postoperative hypocalcemia is the most frequent complication after thyroidectomy. One goal of our study was to investigate the parathyroid hormone (PTH) as the main predictor and early postoperative hypocalcemia. The study prospectively included 135
Externí odkaz:
https://doaj.org/article/67d9106c41cc4cb1bee0d27deb4492ff
Publikováno v:
Эндокринная хирургия, Vol 8, Iss 2, Pp 20-26 (2014)
Beckwith-Wiedemann syndrome (BWS) is a genetic overgrowth disorder involving a predisposition to tumor development. The common features of Beckwith-Wiedemann syndrome include omphalocele, macroglos- sia and macrosomia. The increased risk for neoplasi
Externí odkaz:
https://doaj.org/article/9b4337c0098141f38e5c867f62da3b6c
Publikováno v:
Эндокринная хирургия, Vol 8, Iss 2, Pp 14-19 (2014)
The main difficulty of primary hyperparathyroidism in the surgical aspect, it is possible atypical location of the parathyroid glands and multiple nature of the lesion. Proposed significant number of methods for pre- operative and intraoperative for
Externí odkaz:
https://doaj.org/article/8c324de28f924e33a9db6c636242570a
Publikováno v:
Эндокринная хирургия, Vol 8, Iss 2, Pp 9-13 (2014)
At the present time topical diagnosis of ACTH-producing neuroendocrine tumors of different localization is the most challenging problem for endocrinologists around the world. Despite the significant improvement of existing diagnostic techniques, in 9
Externí odkaz:
https://doaj.org/article/08e8197988af472fb6bfc39113067354
Autor:
G A Melnichenko, I S Stilidi, V A Gorbunova, B Ya Alexeev, D G Beltsevich, A O Raykhman, N S Kuznetsov, N V Zhukov, V Yu Bokhyan
Publikováno v:
Эндокринная хирургия, Vol 8, Iss 1, Pp 4-26 (2014)
Statement of hormonal activity and potential malignancy are the most important issues of diagnosis and selection of appropriate treatment way for patients with adrenal tumors. Adrenal cortical carcinoma (ACC) is rare disease with poor prognosis. Inci
Externí odkaz:
https://doaj.org/article/c29028d2f432430fa8db653865144d62
Autor:
F M Abdulkhabirova, D G Bel'tsevich, V E Vanushko, I I Dedov, N S Kuznetsov, G A Mel'nichenko, N M Platonova, P O Rumyantsev, E A Troshina, A N Tyul'pakov, V V Fadeev, M A Kropotov, L N Lyubchenko, A M Mudunov, S O Podvyaznikov, V G Polyakov, I S Romanov, S Subramanian, S A Tyulyandin, V Zh Brzhezovskiy, A Yu Abrosimov, A A Il'in, P A Isaev, V S Medvedev, U V Rumyantseva, V O Ol'shanskiy, I V Reshetov, A N Makhson, V O Bondarenko, P S Vetshev, D V Zaletaev, Yu V Ivanov, L G Kozhanov, I V Soldatov, S S Kharnas, A S Barchuk, L M Bershteyn, I V Sleptsov, R A Chernikov, A N Bubnov, E N Grineva, G M Manikhas, A F Romanchishen, S V Korenev, I V Vikhlyanov, A D Gashchenko, V V Dvornichenko, A V Kiyaev, V A Privalov, S V Yaytsev, P V Svetitskiy, R Sh Khasanov, V A Tsvetaev, E L Choynzonov, S P Shevchenko
Publikováno v:
Эндокринная хирургия, Vol 7, Iss 2, Pp 4-16 (2013)
Представленные клинические рекомен дации объединяют мнения членов рабочей группы по ключевым и наиболее спорным проблемам диагностик
Externí odkaz:
https://doaj.org/article/20b518f362ce4c0fbfdea11f9e4327ca
Autor:
N S Kuznetsov, E I Marova, O V Remizov, N V Latkina, Voskoboynikov, E A Dobreva, V V Krylov, I A Voronkova
Publikováno v:
Эндокринная хирургия, Vol 7, Iss 2, Pp 39-44 (2013)
Ectopic hormonesecreting of cecum are rare. We report the case of a 52yearold woman with a typical clin ical picture of Cushing disease. Diagnostic tests confirmed ACTH dependent Cushing’s syndrome, which is caused by neuroendocrine tumor of the ce
Externí odkaz:
https://doaj.org/article/a2256853d98d4f1286a10169bd020c11
Autor:
N S Kuznetsov, E I Marova, N V Latkina, E A Dobreva, V V Krylov, L E Kats, O V Remizov, I A Voronkova
Publikováno v:
Эндокринная хирургия, Vol 6, Iss 4, Pp 43-50 (2012)
Ectopic hormone-secreting pheochromocytomas are rare. Only case reports exist in the literature. Despite the large number of guides on diagnosis and treatment of pheochromocytoma, and Cushing syndrome, the extreme rarity of ectopic ACTH-syndrome caus
Externí odkaz:
https://doaj.org/article/70aaf5c637434915a8479bcdc1664730
Publikováno v:
Эндокринная хирургия, Vol 6, Iss 4, Pp 4-10 (2012)
Topical diagnostic methods in ACTH-producing neuroendocrine tumors with various localization. Topical diagnostic of ACTH-producing neuroendocrine tumors is a major stage in management of patients with ACTH-producing syndrome, because one of the main
Externí odkaz:
https://doaj.org/article/99eb4e204d6641c9beb5de94b1f5cabc