Zobrazeno 1 - 10
of 50
pro vyhledávání: '"T I, Subbotina"'
Autor:
T. I. Subbotina, A V Krivtsov, Yu. V. Ichuk, A. L. Smetanin, A I Andriyanov, E. F. Sorokoletova
Publikováno v:
Bulletin of the Russian Military Medical Academy. 22:236-242
Historical materials about the life and work of G.V. Khlopin, an outstanding scientist and hygienist, who created his own large scientific school. The main activity of which was the development of prevention and public hygiene. Biographical data are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::880323beab535beb75462ae68f247766
https://doi.org/10.17816/brmma62834
https://doi.org/10.17816/brmma62834
Autor:
M V Shumikhina, T I Subbotina, M M Litvinova, S Z Nuralieva, T V Filippova, D V Svetlichnaya, I S Chugunov, S L Morozov, Z K Gadzhieva, V I Rudenko
Publikováno v:
Scopus-Elsevier
Kidney stone disease (KSD) is an actual problem of modern health care. By now, more than 80 monogenic forms of urolithiasis have been described. To diagnose such forms of KSD different molecular genetic technologies are used. In the current article 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40c0d9da16181f440e807e92a414e05
https://doi.org/10.18565/urology.2020.3.81-86
https://doi.org/10.18565/urology.2020.3.81-86
Autor:
Yuri Alyaev, V I Rudenko, D V Svetlichnaya, M M Litvinova, T I Subbotina, Z K Gadzhieva, E G Tadevosyan, T V Filippova, A Y Asanov, K R Khamidullin, M M Azova, A M Pushkarev
Publikováno v:
Urologiia. :125-130
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease. The mutations in the AGXT, GRHPR, HOGA1 genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c1abe91cffbb58c79bb7c3ac7820fd17
https://doi.org/10.18565/urology.2019.6.125-130
https://doi.org/10.18565/urology.2019.6.125-130
Autor:
Yuri Alyaev, V I Rudenko, T I Subbotina, Z K Gadzhieva, D V Svetlichnaya, A Y Asanov, M V Shumikhina, M M Azova, T V Filippova, M M Litvinova
Publikováno v:
Urologiia. :140-143
Primary hyperoxaluria is a group of inherited metabolic diseases characterized by increased formation of calcium-oxalate stones in kidneys with development of nephrolithiasis and chronic kidney disease. The article summarizes the modern information o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2db88ec79ffb72e0868632aaa49736f
https://doi.org/10.18565/urology.2019.5.140-143
https://doi.org/10.18565/urology.2019.5.140-143
Autor:
Yu. V. Ishchyk, I A Konovalova, A I Andriyanov, V V Sochenko, A V Krivtsov, N V Yurchik, A. L. Smetanin, T I Subbotina, V P Andreev
Publikováno v:
Bulletin of the Russian Military Medical Academy. 20:139-143
The nutrition of food for the crews of surface ships (vessels) of the Navy in a long sea cruise was studied to assess the energy and plastic adequacy of the current diet. The indicators of the chemical composition and energy value of the average dail
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f480df39c36e04861f0f6166765b9bb0
https://doi.org/10.17816/brmma12297
https://doi.org/10.17816/brmma12297
Autor:
N S Shishkina, Vera Anatol'evna Gorelysheva, E M Sementsova, T I Subbotina, Olga Mikhailovna Smirnova, Ivan Ivanovich Dedov
Publikováno v:
Сахарный диабет, Vol 7, Iss 4, Pp 34-36 (2004)
Сахарный диабет (СД) часто ассоциирован с различными генетическими синдромами. Доля лиц с генетическими синдромами, сопровождающимися
Externí odkaz:
https://doaj.org/article/5a4b54ae1e6648f5927b02afedef64b7
Autor:
T V, Filippova, D V, Svetlichnaya, V I, Rudenko, Y G, Alyaev, E G, Tadevosyan, M M, Azova, T I, Subbotina, Z K, Gadzhieva, A Y, Asanov, K R, Khamidullin, A M, Pushkarev, M M, Litvinova
Publikováno v:
Urologiia (Moscow, Russia : 1999). (6)
Primary hyperoxaluria is a group of rare inherited diseases characterized by impaired oxalate metabolism with the early manifestation of urolithiasis and the development of the chronic kidney disease. The mutations in the AGXT, GRHPR, HOGA1 genes are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abe8ed86cd176295bec14271ea9839eb
https://pubmed.ncbi.nlm.nih.gov/32003182
https://pubmed.ncbi.nlm.nih.gov/32003182
Autor:
T I Subbotina, M M Litvinova, A Yu Asanov, V I Rudenko, Leonid Rapoport, Kamil Khafizov, T V Filippova, Z K Gadzhieva, Yu B Kazilov
Publikováno v:
Urologiia. :154-160
The article presents pooled results of domestic and international studies investigating genetic aspects of urolithiasis associated with impaired calcium metabolism. The review highlights the importance of early and accurate diagnosis of hereditary di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11a704f38262cca35b9d7b00d658fa2b
https://doi.org/10.18565/urology.2018.4.154-160
https://doi.org/10.18565/urology.2018.4.154-160
Autor:
A. L. Smetanin, A I Andriyanov, I A Konovalova, T. I. Subbotina, O. G. Korosteleva, V. I. Polyakov, N. A. Tshukina
Publikováno v:
Marine Medicine. 4:75-82
The dynamics of indicators of the component composition of the seamen’s organism of the surface ship of the Navy in the conditions of a long march in interaction with the crew’s feeding habits is considered in the article. The actual nutrition of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6740a8eed51ec504c7cb19f3a9086050
https://doi.org/10.22328/2413-5747-2018-4-3-75-82
https://doi.org/10.22328/2413-5747-2018-4-3-75-82
Autor:
T V, Filippova, D V, Svetlichnaya, V I, Rudenko, Y G, Alyaev, M V, Shumikhina, M M, Azova, T I, Subbotina, Z K, Gadzhieva, A Yu, Asanov, M M, Litvinova
Publikováno v:
Urologiia (Moscow, Russia : 1999). (5)
Primary hyperoxaluria is a group of inherited metabolic diseases characterized by increased formation of calcium-oxalate stones in kidneys with development of nephrolithiasis and chronic kidney disease. The article summarizes the modern information o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88c5cf3a4ef4948b6b2c60e194c56b09
https://pubmed.ncbi.nlm.nih.gov/31808650
https://pubmed.ncbi.nlm.nih.gov/31808650