Zobrazeno 1 - 10
of 25
pro vyhledávání: '"L. I. Zilberman"'
Autor:
E. A. Sechko, E. M. Romanenkova, I. A. Eremina, L. I. Zilberman, L. V. Nikankina, Z. T. Zuraeva, O. B. Bezlepkina, V. A. Peterkova, D. N. Laptev
Publikováno v:
Сахарный диабет, Vol 25, Iss 5, Pp 449-457 (2022)
BACKGROUND: T1D is characterized by autoimmune destruction of pancreatic β-cells, which develops due to genetic and environmental risk factors. Shortly after initiating the treatment with insulin, 80% of children with T1D may require smaller doses o
Externí odkaz:
https://doaj.org/article/2ccbc67cff294dadb606633ddbabed81
Feсal microbiota transplantation in the format of complex therapy in obesive siblings: clinical case
Autor:
E. V. Pokrovskaya, E. S. Zhgun, E. A. Shestakova, I. A. Sklyanik, I. V. Fedushkina, E. I. Olekhnovich, D. N. Konanov, D. A. Kardonsky, Yu. V. Kislun, E. A. Sorokina, L. I. Zilberman, N. V. Zaytseva, E. N. Ilina, V. M. Govorun, M. V. Shestakova
Publikováno v:
Сахарный диабет, Vol 25, Iss 4, Pp 405-417 (2022)
Obesity and associated metabolic diseases are often accompanied by changes in the gut microbiota leading to metagenome gene diversity decrease. Fecal microbiota transplantation (FMT) is one of the most effective methods for correcting the intestinal
Externí odkaz:
https://doaj.org/article/1921d8662c654e4ca3b0491ea026d1b9
Autor:
E. A. Sechko, T. L. Kuraeva, L. I. Zilberman, D. N. Laptev, O. B. Bezlepkina, V. A. Peterkova
Publikováno v:
Сахарный диабет, Vol 25, Iss 2, Pp 145-154 (2022)
BACKGROUND: Monogenic diabetes mellitus (MDM) is a rare form of diabetes mellitus (DM) which caused by one or more mutations in one of the genes that cause pancreatic β-cell dysfunction. Despite the sufficient knowledge of the most common subtypes o
Externí odkaz:
https://doaj.org/article/0a1ea31930b74524921be7eafbdbe310
Autor:
E. A. Sechko, T. L. Kuraeva, E. A. Andrianova, L. I. Zilberman, A. O. Emelyanov, D. N. Laptev, O. B. Bezlepkina
Publikováno v:
Сахарный диабет, Vol 25, Iss 1, Pp 89-94 (2022)
MODY10 is a rare subtype of MODY diabetes, which caused by heterozygous mutations in the insulin gene INS. There are single descriptions of families with MODY-INS or MODY10 in the literature, its clinical course is not well understood. We present a c
Externí odkaz:
https://doaj.org/article/ae03fbd1ad3b496ca56912e6c03fd27b
Autor:
D. N. Laptev, A. O. Emelyanov, E. A. Andrianova, L. I. Zilberman, I. A. Eremina, G. N. Svetlova, E. V. Titovich, O. B. Bezlepkina, V. A. Peterkova
Publikováno v:
Сахарный диабет, Vol 24, Iss 6, Pp 504-510 (2022)
BACKGROUND: In 2018, a Frestyle Libre flash glucose monitoring system (FGM) appeared in Russia and became a potential alternative to the traditional CGM. Studies carried out to date have shown the advantages of FGM over SMBG, but only a few of them r
Externí odkaz:
https://doaj.org/article/11c965ef837642ccb517c1bf34e242ff
Autor:
Yu. V. Tikhonovich, E. E. Petryaykina, A. V. Timofeev, N. A. Zubkova, A. A. Kolodkina, E. L. Sorkina, E. V. Vasiliev, V. M. Petrov, E. A. Andrianova, L. I. Zilberman, G. N. Svetlova, A. L. Кalinin, P. M. Rubtsov, S. L. Кiselev, A. V. Panova, E. V. Shreder, T. S. Krasnova, B. P. Kulieva, I. V. Gariaeva, I. G. Rybkina, O. A. Malievskiy, A. N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 24, Iss 5, Pp 414-421 (2022)
Background: Currently more than 50 mutations of the INS gene are known to affect the various stages of insulin biosynthesis in the beta cells of the pancreas. However only individual cases of diabetes mellitus (DM) associated with heterozygous mutati
Externí odkaz:
https://doaj.org/article/c8fca7154b1248a094e058083772590f
Autor:
D. N. Laptev, A. O. Emelyanov, E. A. Andrianova, L. I. Zilberman, I. A. Eremina, G. N. Svetlova, E. V. Titovich, O. B. Bezlepkina, V. A. Peterkova
Publikováno v:
Сахарный диабет, Vol 24, Iss 6, Pp 504-510 (2022)
BACKGROUND: In 2018, a Frestyle Libre flash glucose monitoring system (FGM) appeared in Russia and became a potential alternative to the traditional CGM. Studies carried out to date have shown the advantages of FGM over SMBG, but only a few of them r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c685e2a3aac87e08179411464f3d27b2
https://doi.org/10.14341/dm12817
https://doi.org/10.14341/dm12817
Autor:
L. I. Zilberman, Irina Eremina, Valentina Alexandrovna Peterkova, Dimitry A. Chistiakov, Tamara Leonidovna Kuraeva, Alexei N. Brovkin, Irina A. Dubinina, Ivan Ivanovich Dedov, Alexei G. Nikitin, Valery V. Nosikov
Publikováno v:
Diabetes & Metabolic Syndrome: Clinical Research & Reviews. 8:133-137
Identification of metabolic and genetic factors capable to mediate progression from normal glucose tolerance (NGT) through impaired glucose tolerance (IGT) to type 2 diabetes (T2D) in childhood obesity.Three groups of obese children with NGT (n=54),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a71e4186b2d3ee4d689bc360107c8ca
https://doi.org/10.1016/j.dsx.2014.07.002
https://doi.org/10.1016/j.dsx.2014.07.002
Autor:
Valentina Alexandrovna Peterkova, Tamara Leonidovna Kuraeva, Aleksey Georgievich Nikitin, Valery V. Nosikov, Elena Yur'evna Lavrikova, Ivan Ivanovich Dedov, Nana Mikhailovna Tsitlidze, Yury Alexandrovich Seregin, L. I. Zilberman
Publikováno v:
Сахарный диабет, Vol 13, Iss 2, Pp 17-20 (2010)
Aim. To analyse frequency distribution of alleles and genotypes of -23 HphI, a polymorphic marker of the INS gene, for evaluation of its associationwith DM1. Materials and methods. The study included two group of subjects: healthy ones and DM1 patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96f17f80697cb0a367905482440b6bef
https://doi.org/10.14341/2072-0351-5668
https://doi.org/10.14341/2072-0351-5668
Autor:
Tamara Leonidovna Kuraeva, L. I. Zilberman, Valentina Peterkova, N. M. Tzitlidze, Elena Yur'evna Lavrikova, Ivan Ivanovich Dedov, Alexey Nikitin, Yu. A. Seregin, Nosikov Vv
Publikováno v:
Molecular Biology. 44:228-232
To study the association with diabetes mellitus type 1, we analyzed the distribution of allele and genotype frequencies of polymorphic marker rs2292239 of ERBB3 gene, encoding epidermal growth factor receptor type 3 and polymorphic marker rs3184504 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04794ec4679ba036704eebb9698fa9c3
https://doi.org/10.1134/s002689331002007x
https://doi.org/10.1134/s002689331002007x