Zobrazeno 1 - 10
of 33
pro vyhledávání: '"A N Tyulpakov"'
Autor:
E O Mamedova, N G Mokrysheva, E A Pigarova, E G Przhiyalkovskaya, I A Voronkova, E V Vasilyev, V M Petrov, V A Gorbunova, L Ya Rozhinskaya, Zh E Belaya, A N Tyulpakov
Publikováno v:
Терапевтический архив, Vol 88, Iss 10, Pp 57-62 (2016)
The article describes two clinical cases of severe primary hyperparathyroidism (PHPT) caused by parathyroid carcinoma in young female patients who underwent molecular genetic testing to rule out the hereditary forms of PHPT. In both patients, heteroz
Externí odkaz:
https://doaj.org/article/38ae1e1d8f9441e8beb204f3d5ea36c7
Publikováno v:
Терапевтический архив, Vol 87, Iss 3, Pp 83-87 (2015)
Hereditary lipodystrophies (HLD) are a heterogeneous group of rare diseases characterized by a complete or partial loss of subcutaneous fat and by the development of metabolic disturbances: diabetes mellitus with obvious insulin resistance and acanth
Externí odkaz:
https://doaj.org/article/d1e16c3d847c4cbca4e0974fa86d1ee1
Autor:
Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 25, Iss 1, Pp 81-88 (2022)
Mutations in the GLIS3 gene encoding the GLIS3 transcription factor are cause of a rare syndromic form of neonatal diabetes mellitus (NDM) with congenital hypothyroidism. Additional features include congenital glaucoma, hepatic fibrosis, polycystic k
Externí odkaz:
https://doaj.org/article/15276206fcaa42249961e40a5ce1fb10
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:
Irina V. Kononenko, Anastasiya A. Glibka, Natalya A. Zubkova, Alexander Y. Mayorov, Anatoly N. Tyulpakov, Olga M. Schmidt
Publikováno v:
Сахарный диабет, Vol 22, Iss 4, Pp 384-391 (2019)
Approximately 90% of all cases of diabetes mellitus in adults involve type 2 diabetes, while the prevalence of maturity-onset diabetes of the young (MODY) remains undetermined leading to inappropriate treatment regimens. One of the most common monoge
Externí odkaz:
https://doaj.org/article/687734329d874d88b6d54f1e843edee5
Autor:
Sergey N. Lysenko, Marina A. Chechneva, Fatima F. Burumkulova, Vasily A. Petrukhin, Anton E. Panov, Margarita A. Plechanova, Victoria I. Ulyatovskaya, Natalia A. Zubkova, Anatoliy N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 22, Iss 4, Pp 358-366 (2019)
BACKGROUND: The basis of early ultrasound (US) diagnosis of diabetic fetopathy (DF) in pregnant with gestational diabetes mellitus (GDM) is the forehanded detection of macrosomia, especially its asymmetric forms. In pregnant with GDM on a diet therap
Externí odkaz:
https://doaj.org/article/b0478a24092941008369ed5de1b04b8f
Autor:
Natalia A. Zubkova, Fatima F. Burumkulova, Vasily A. Petrukhin, Margarita A. Plechanova, Anton E. Panov, Evgeny V. Vasilyev, Vasily M. Petrov, Nina A. Makretskaya, Anatoliy N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 22, Iss 3, Pp 274-280 (2019)
MODY1 and MODY3 represent rare causes of diabetes in pregnancy. Establishing a molecular diagnosis of MODY1 or MODY3 during pregnancy may be important for minimizing risk of perinatal complications and for improving glycemic control after pregnancy.
Externí odkaz:
https://doaj.org/article/e0311204822549d6a1dc1c0e345dbe75
Autor:
Nina A. Makretskaya, Olga B. Bezlepkina, Anna A. Kolodkina, Alexey V. Kiyaev, Evgeny V. Vasilyev, Vasily M. Petrov, Olga A. Chikulaeva, Oleg A. Malievsky, Ivan I. Dedov, Anatoliy N. Tyulpakov
Publikováno v:
Клиническая и экспериментальная тиреоидология, Vol 14, Iss 2, Pp 64-71 (2018)
Congenital hypothyroidism is a heterogeneous group of diseases, which is manifested by loss of function of the thyroid gland that affects infants from birth. 8085% of cases are due to different types of thyroid dysgenesis. 5 genes have been described
Externí odkaz:
https://doaj.org/article/cd8d17dae145417982f86e830ab25c5f
Autor:
Marina S. Sheremeta, Ekaterina A. Pigarova, Kristina S. Kulikova, Irina M. Belovalova, Anatoliy N. Tyulpakov, Pavel O. Rumiantsev
Publikováno v:
Ожирение и метаболизм, Vol 14, Iss 4, Pp 77-82 (2017)
Osteogenesis imperfecta (OI) – is a group of genetically disorders, which are charaterized by a disturbed bone formation. In turn, the excess of thyroid hormones in Graves' disease (GD) also posses a negative effect on bone tissue, thereby aggravat
Externí odkaz:
https://doaj.org/article/3102796a1f7346d8ab36aa9b1a0705ee
Autor:
Anastasiya A. Glibka, Irina Vladimirovna Kononenko, Alexander Yur'evich Mayorov, Anatoly N. Tyulpakov, Olga M. Schmidt, Natalya A. Zubkova
Publikováno v:
Сахарный диабет, Vol 22, Iss 4, Pp 384-391 (2019)
Approximately 90% of all cases of diabetes mellitus in adults involve type 2 diabetes, while the prevalence of maturity-onset diabetes of the young (MODY) remains undetermined leading to inappropriate treatment regimens. One of the most common monoge