Zobrazeno 1 - 7
of 7
pro vyhledávání: '"N. Y. Kashirskaya"'
Autor:
N. V. Petrova, N. Y. Kashirskaya, D. K. Saydaeva, A. V. Polyakov, T.A. Adyan, O. I. Simonova, Y. V. Gorinova, E. I. Kondratyeva, V. D. Sherman, O. G. Novoselova, T. A. Vasilyeva, A. V. Marakhonov, M. Macek, E. K. Ginter, R. A. Zinchenko
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Cystic fibrosis (CF; OMIM #219700) is a common autosomal recessive disease caused by pathogenic variants (henceforward mutations) in the cystic fibrosis transmembrane conductance regulator gene (CFTR). The spectrum and frequencies
Externí odkaz:
https://doaj.org/article/592070c75b8342d5ae78cf9010e42d83
Autor:
S. A. Repina, S. A. Krasovsky, R. V. Rozhivanov, T. M. Sorokina, L. V. Shileiko, M. I. Shtaut, L. F. Kurilo, G. V. Shmarina, T. A. Adyan, N. Y. Kashirskaya, A. V. Polyakov, V. B. Chernykh
Publikováno v:
Андрология и генитальная хирургия, Vol 19, Iss 2, Pp 31-39 (2018)
Introduction. Cystic fibrosis (CF) is common monogenic disease resulted from CFTR gene mutations. A most of CF male patients are infertile due to the obstructive azoospermia, however, the mechanisms of the reduced fertility in male patients without t
Externí odkaz:
https://doaj.org/article/8b0ec55e0eca4a99b1a6b27e482bd461
Autor:
V. D. Sherman, E. I. Kondratieva, A. Y. Voronkova, N. Y. Kashirskaya, L. A. Shabalova, V. S. Nikonova, E. K. Zhekaite, S. I. Kutsev
Publikováno v:
Медицинский совет, Vol 0, Iss 18, Pp 124-128 (2017)
Study objective: comparative evaluation of clinical status of patients with cystic fibrosis (CF) 6–9 years, the diagnosis of which was established before the start of neonatal screening (NS) for MV in the Moscow region and in same age group since t
Externí odkaz:
https://doaj.org/article/946811a28f8543908e247106ef41bf70
Autor:
S. V. POLIKARPOVA, E. I. KONDRATYEVA, L. A. SHABALOVA, N. V. PIVKINA, S. V. ZHILINA, A. Y. VORONKOVA, V. D. SHERMAN, V. S. NIKONOVA, N. I. KAPRANOV, N. Y. KASHIRSKAYA, S. Y. SEMYKIN, E. L. AMELINA, S. A. KRASOVSKY
Publikováno v:
Медицинский совет, Vol 0, Iss 15, Pp 84-89 (2016)
Chronic lower respiratory tract infection in patients with cystic fibrosis (CF) is the major factor determining the severity of the clinical course and prognosis of the disease. The purpose of the study was to investigate the prevailing respiratory m
Externí odkaz:
https://doaj.org/article/9fde4088c52346b292623b7a73c2d83c
Autor:
A. A. Baranov, L. S. Namazova-Baranova, O. I. Simonova, N. Y. Kashirskaya, E. A. Roslavtseva, Y. V. Gorinova, S. A. Krasovskiy, L. R. Selimzyanova
Publikováno v:
Педиатрическая фармакология, Vol 12, Iss 5, Pp 589-604 (2015)
The issue of contemporary diagnosis and correct management of patients with cystic fibrosis is relevant not only for Russia, but for the entire world. Despite achievements of the contemporary medical science, underdiagnosis of this systemic genetic d
Externí odkaz:
https://doaj.org/article/25b4323c3fe54c1cbf697cbaa9f40a59
Publikováno v:
Педиатрическая фармакология, Vol 10, Iss 6, Pp 53-60 (2013)
The article is dedicated to historical and modern trials in the sphere of mucoviscidosis in Russia, peculiarities of clinical manifestations, pathophysiological and pathomorphological disorders and of the disease course with the analysis of the first
Externí odkaz:
https://doaj.org/article/30ce49665a1b4b69bd1971897f163601
Publikováno v:
POMICULTURE & SMALL FRUITS CULTURE IN RUSSIA. 54:278-282
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b38b5ae4f3fa802c83bece4bae198f0d
https://doi.org/10.31676/2073-4948-2018-54-278-282
https://doi.org/10.31676/2073-4948-2018-54-278-282