Zobrazeno 1 - 10
of 41
pro vyhledávání: '"M. Yu. Yukina"'
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 136-150 (2024)
BACKGROUND: Recent clinical descriptions have shown that in adult patients, the cause of nondiabetic hypoglycemia (NDH) may be various genetically determined disorders of glucose metabolism or insulin synthesis/bioavailability. In this connection, in
Externí odkaz:
https://doaj.org/article/82cfad1378454f13a965b51d69eabf4b
Autor:
M. Yu. Yukina, E. A. Troshina, N. F. Nuralieva, S. V. Popov, O. Yu. Rebrova, N. G. Mokrysheva
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 4, Pp 338-354 (2024)
BACKGROUND: It is known that insulinoma in approximately 5% of cases is associated with multiple endocrine neoplasia type 1 syndrome (MEN1), in which the prognosis and management tactics of patients have been developed in detail. The diagnosis of MEN
Externí odkaz:
https://doaj.org/article/07a39f07ae8e42e0942304fd6743fff7
Autor:
N. V. Molashenko, N. Yu. Kalinchenko, V. A. Ioutsi, O. S. Gurinovich, D. M. Babaeva, A. A. Voznesenskaya, N. M. Platonova, M. Yu. Yukina, A. A. Kolodkina, T. A. Ponomareva
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 1, Pp 73-83 (2023)
17β-Hydroxysteroid dehydrogenase 3 deficiency (17HSD3) is a rare autosomal recessive cause of 46, XY disorders of sex development resulting from HSD17B3 gene mutations, in which conversion of androstenedione to testosterone is impared. The clinical
Externí odkaz:
https://doaj.org/article/9943d6f6e4f944f4b670ce9657dd76d4
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 1, Pp 43-48 (2023)
BACKGROUND: Insulinoma is a pancreatic neuroendocrine tumor that manifests by impaired carbohydrate metabolism with the development of hypoglycemic syndrome. The instrumental methods used at the present stage do not always make it possible to identif
Externí odkaz:
https://doaj.org/article/f662b164a5384cd9a50fbd164e93ea00
Publikováno v:
Ожирение и метаболизм, Vol 19, Iss 2, Pp 134-141 (2022)
Background: The diagnostic threshold of β-hydroxybutyrate (BHB) at the moment of hypoglycemia in insulinoma was developed for venous blood many years ago, when there were no alternative ways to measure ketones. Number of works, mainly on patients wi
Externí odkaz:
https://doaj.org/article/3cf31834b3604f4391cc26668028d578
Autor:
M. Yu. Yukina, V. R. Mustafina, E. V. Vasilyev, E. A. Troshina, N. M. Platonova, D. G. Beltsevich
Publikováno v:
Медицинский совет, Vol 0, Iss 7, Pp 150-154 (2021)
Pheochromocytoma/paraganglioma is a neuroendocrine tumor of chromaffin and nonchromaffin cells of the autonomic nervous system, in most cases localized in the medullary layer of the adrenal gland. Its development is often associated with genetic pred
Externí odkaz:
https://doaj.org/article/64d9aa005006432183cb570b2bee2f6c
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 48, Iss 7, Pp 445-458 (2020)
Rationale: In Russia, assessment of anti-P450c21 antibodies (AB) in the diagnosis of autoimmune adrenal insufficiency (AAI) has not been commonly used, and the disease screening has not been implemented.Aims: 1) To determine the sensitivity and speci
Externí odkaz:
https://doaj.org/article/f3deee626e0745828e18d131fc8aa531
Autor:
M. Yu. Yukina, M. O. Chernova, N. F. Nuralieva, A. K. Eremkina, E. A. Troshina, G. A. Melnichenko, N. G. Mokrysheva
Publikováno v:
Ожирение и метаболизм, Vol 17, Iss 4, Pp 357-368 (2020)
Adrenal insufficiency (AI) is a syndrome caused by disturbance in the synthesis and secretion of hormones of the adrenal cortex, which ensure the vital activity, energy and water-salt homeostasis. The widest hormonal deficiency is observed in primary
Externí odkaz:
https://doaj.org/article/992c45b539b04c5ebb9a58a8e04ffb62
Autor:
E. A. Troshina, V. A. Volnukhin, V. A. Petrov, N. F. Nuralieva, M. Yu. Yukina, E. M. Orlova, N. V. Frigo
Publikováno v:
Терапевтический архив, Vol 92, Iss 10, Pp 88-96 (2020)
Vitiligo is a common polygenic autoimmune disease in which the foci of depigmentation are formed on the skin and/or mucous membranes as a result of the death of melanocytes. There are several hypotheses for the pathogenesis of the disease, the leadin
Externí odkaz:
https://doaj.org/article/d112e72029c947f59c2ed7900b4557a6
Publikováno v:
Медицинский совет, Vol 0, Iss 7, Pp 130-136 (2020)
Hypoglycemic syndrome (HGS) is a significant decrease glucose in blood, manifested by neurological symptoms, and stopped by the introduction of glucose. Among the many causes of HGS the special place is taken by the factitious hypoglycemia, as one of
Externí odkaz:
https://doaj.org/article/05796f51c33e4087892b09dab941c938