Zobrazeno 1 - 10
of 20
pro vyhledávání: '"E G, Przhiyalkovskaya"'
Autor:
E. G. Przhiyalkovskaya, N. G. Mokrysheva, E. A. Troshina, G. A. Melnichenko, I. I. Dedov, M. B. Antsiferov, L. I. Astafieva, T. P. Bardymova, Zh. E. Belaya, G. R. Vagapova, S. Yu. Vorotnikova, A. Yu. Grigoriev, E. N. Grineva, L. K. Dzeranova, I. A. Ilovaiskaya, P. L. Kalinin, A. M. Lapshina, A. S. Lutsenko, E. O. Mamedova, E. I. Marova, M. A. Perepelova, E. A. Pigarova, V. S. Pronin, L. Ya. Rozhinskaya, Yu. Yu. Trunin, A. S. Shutova
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 215-249 (2024)
We recommend acromegaly to be ruled in all patients with characteristic changes in appearance (A3). In all patients without characteristic changes in appearance, we recommend to rule out acromegaly, if several clinical signs suspicious for acromegaly
Externí odkaz:
https://doaj.org/article/0e53e7cc97e84856a75fa6c849e035d8
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 195-204 (2024)
Acromegaly is a rare neuroendocrine disease caused by excessive production of growth hormone (GH), which acts as a trigger for cartilage tissue destruction leading to joint damage.Patients with acromegaly, especially in the active stage, often compla
Externí odkaz:
https://doaj.org/article/9d04378f9ccf423d86cb552c355b794d
Autor:
A. A. Almaskhanova, K. V. Melkozerov, E. G. Przhiyalkovskaya, N. V. Tarbaeva, R. S. Kosharnaia, I. S. Gomova, P. A. Alferova, L. Ya. Rozhinskaya, V. Y. Kalashnikov, Zh. E. Belaya, G. A. Melnichenko, N. G. Mokrysheva
Publikováno v:
Рациональная фармакотерапия в кардиологии, Vol 20, Iss 3, Pp 349-356 (2024)
The most common causes of death in acromegaly are cardiovascular diseases (about 60%). Heart arrhythmias and conduction disorders lead to sudden cardiac death (SCD). In this article, we described a clinical case about preventing SCD in a patient with
Externí odkaz:
https://doaj.org/article/3edf616007344eb78810a9560bc3088e
Autor:
E. A. Starostina, N. V. Frolkova, S. M. Seidova, E. G. Przhiyalkovskaya, N. M. Platonova, E. A. Troshina
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 1, Pp 85-91 (2024)
Androgen insensitivity syndrome is a genetic disorder characterized by complete or partial androgen insensitivity in individuals with a 46XY genotype. It is also the most common cause of disorders of sexual differentiation in patients with a 46XY kar
Externí odkaz:
https://doaj.org/article/5144fcf6dcda4eeba83686269ff64fe4
Autor:
A. S. Lutsenko, E. G. Przhiyalkovskaya, O. K. Vikulova, M. A. Isakov, Zh. E. Belaya, L. Ya. Rozhinskaya, E. A. Pigarova, L. K. Dzeranova, E. I. Marova, G. A. Melnichenko, N. M. Platonova, E. A. Troshina, N. G. Mokrysheva
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 4, Pp 318-329 (2024)
BACKGROUND: Pituitary adenomas are the third most common intracranial neoplasm. Clinical significance is determined by the nature of growth and hormonal activity, leading to disruption of various parts of metabolism. Medical registries are a valuable
Externí odkaz:
https://doaj.org/article/3c8fb017bc52413f98ecfcac654d7e6f
Autor:
E. A. Starostina, N. V. Frolkova, S. M. Seidova, E. G. Przhiyalkovskaya, N. M. Platonova, E. A. Troshina
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 172-173 (2024)
A corrigendum on "Androgen insensitivity syndrome: preventive gonadectomy, "pros" and "cons"" (Obesity and metabolism by Еvgenia A. Starostina, Nadezhda V. Frolkova, Seidbike M. Seidova, Elena G. Przhiyalkovskaya, Nadezhda M. Platonova (2024). Obesi
Externí odkaz:
https://doaj.org/article/ddb3f423a32144809f6502b9eb633db3
Autor:
A. S. Shutova, E. A. Fedina, A. G. Kuzmin, E. A. Pigarova, E. G. Przhiyalkovskaya, E. E. Litvinova, N. A. Shutova, L. K. Dzeranova
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 3, Pp 269-273 (2023)
This article presents a non-standard clinical case of non-obvious causes of secondary osteoporosis in the routine practice of an outpatient and inpatient endocrinologist. This work demonstrates a rather rare situation, including the identification of
Externí odkaz:
https://doaj.org/article/68a8777e9877458babde36cc3da2eccf
Autor:
I. I. Dedov, G. A. Melnichenko, L. K. Dzeranova, E. N. Andreeva, E. N. Grineva, E. I. Marova, N. G. Mokrysheva, E. A. Pigarova, S. Y. Vorotnikova, N. S. Fedorova, A. S. Shutova, E. G. Przhiyalkovskaya, I. A. Ilovaуskaya, T. I. Romantsova, S. A. Dogadin, L. A. Suplotova
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 2, Pp 170-188 (2023)
Hyperprolactinemia is a persistent excess of the blood serum prolactin. The syndrome contains various symptoms, the most characteristic is a violation of the reproductive system. There are multiple endogenous and exogenous causes of hyperprolactinemi
Externí odkaz:
https://doaj.org/article/e66ae6be2b924d338bf260ee24a3b32a
Autor:
L. K. Dzeranova, M. I. Yevloyeva, M. A. Perepelova, E. A. Pigarova, A. S. Shutova, A. V. Dorovskikh, V. N. Azizyan, E. G. Przhiyalkovskaya
Publikováno v:
Ожирение и метаболизм, Vol 20, Iss 1, Pp 66-72 (2023)
Acromegaly is a severe neuroendocrine disease characterized by hypersecretion of growth hormone (GH) caused in 95% of cases by pituitary adenoma, which leads to the development of pathology of various organs and systems. The severity of the condition
Externí odkaz:
https://doaj.org/article/ad0f04113fc14f3b918d8d28dea9a6b5
Autor:
L. K. Dzeranova, A. V. Dorovskikh, E. A. Pigarova, E. G. Przhiyalkovskaya, A. S. Shutova, M. I. Yevloyeva, A. Yu. Grigoriev, V. N. Azizyan, O. V. Ivashchenko
Publikováno v:
Ожирение и метаболизм, Vol 19, Iss 2, Pp 189-197 (2022)
Acromegaly is a severe neuroendocrine disease caused by chronic excessive production of somatotropic hormone (STH), characterized by specific changes in appearance, metabolic disorders. In 95% of cases, the cause of pathology is STH-producing pituita
Externí odkaz:
https://doaj.org/article/6806f244e9c1450783f54aea88943fc9