Zobrazeno 1 - 5
of 5
pro vyhledávání: '"V. S. Tikhonova"'
Publikováno v:
Архивъ внутренней медицины, Vol 13, Iss 5, Pp 392-400 (2023)
Zinner syndrome is a rare congenital anomaly of the mesonephric duct, characterized by a triad of symptoms: seminal vesicle cysts, ipsilateral renal agenesis and ejaculatory duct obstruction. This leads to a severe complication — oligozoospermia/az
Externí odkaz:
https://doaj.org/article/6d9b53f8ad0d46958ea30a2f1b689bc1
Autor:
E. N. Gasanov, E. V. Shpot, A. A. Magomedov, D. V. Chinenov, A. V. Proskura, P. I. Golovnya, E. S. Kapralova, V. S. Tikhonova, L. M. Rapoport
Publikováno v:
Андрология и генитальная хирургия, Vol 22, Iss 4, Pp 60-67 (2021)
The study objective is to improve results of treatment of patients with low-risk prostate cancer (PC).Materials and methods. In the study, comparative analysis of data from 84 patients with low-risk PC was performed: 40 patients were included in the
Externí odkaz:
https://doaj.org/article/1eb69b35f20a4b31a1a902e7b513e5bf
Autor:
I. S. Gruzdev, G. G. Karmazanovsky, M. G. Lapteva, K. A. Zamyatina, V. S. Tikhonova, E. V. Kondratyev, V. Yu. Struchkov, A. V. Glotov, I. S. Proskuryakov, D. V. Podluzhny, A. Sh. Revishvili
Publikováno v:
Medical Visualization. 26:102-109
Objective: to develop a diagnostic model that includes CT and radiomic features for the differential diagnosis of pancreatic neuroendocrine tumors (PNETs) G1 and G2 and pancreatic renal cell carcinoma (RCC) metastases.Material and Methods. 78 patient
Publikováno v:
Medical Visualization.
Purpose. Improving the efficiency of CT in the differential diagnosis of mass-forming pancreatitis (MFP) and pancreatic ductal adenocarcinoma (PDAC) making a diagnostic model based using a combination of texture features and contrast enhancement feat
Autor:
V S Tikhonova, A N Voytovich, A V Kamaev, T E Ivashchenko, A V Orlov, L A Zhelenina, D S Korostovtsev, V I Larionova, A N Voitovich, T E Ivaschenko, D S Korostovsev
Publikováno v:
Russian Journal of Allergy. 8:24-27
Background. To detect sixteen cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations most common to Russian populations in children with severe asthma (SA). Patients and Methods. S A group included 59 children aged 4-17 years old (