Zobrazeno 1 - 10
of 619
pro vyhledávání: '"Kalinchenko, A."'
Autor:
Ekaterina Kim, Natalia Kalinchenko, Anna Eremkina, Liliya Urusova, Rustam Salimkhanov, Natalia Mokrysheva
Publikováno v:
Therapeutic Advances in Medical Oncology, Vol 16 (2024)
Parathyroid carcinoma (PC) is extremely rare in children and adolescent. PC is more often sporadic, but also it could be associated with germline mutations. The clinical features of primary hyperparathyroidism (PHPT) are nonspecific in children and a
Externí odkaz:
https://doaj.org/article/3fe57714d1d1419c94d56bc47822d5b1
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
Autor:
Nina Makretskaya, Natalia Kalinchenko, Inna Tebieva, Sofya Ionova, Rena Zinchenko, Andrey Marakhonov, Anatoly Tiulpakov
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundCongenital adrenal hyperplasia (CAH) caused by 3β-HSD deficiency is a rare form of congenital adrenal deficiency with an autosomal recessive type of inheritance. Previously we have demonstrated that a single nucleotide variant (SNV) p.Trp2
Externí odkaz:
https://doaj.org/article/5e5c7612678946a68f9a3c87d1f9c23b
Autor:
Kim, Ekaterina, Kalinchenko, Natalia, Eremkina, Anna, Urusova, Liliya, Salimkhanov, Rustam, Mokrysheva, Natalia
Publikováno v:
Therapeutic Advances in Medical Oncology; 8/1/2024, p1-14, 14p
Publikováno v:
Juvenis Scientia, Vol 7, Iss 6, Pp 6-16 (2021)
The development of metabolic disorders occurs in psoriasis: insulin resistance, systemic inflammation, atherosclerosis, oxidative stress and obesity. The paper presents pathological biochemical pathways of metabolic disorders development which is cau
Externí odkaz:
https://doaj.org/article/86cc9e48e83c4094a6083db679cefe0a
Autor:
N. G. Mokrysheva, G. A. Melnichenko, L. V. Adamyan, E. A. Troshina, N. V. Molashenko, A. I. Sazonova, E V. Uvarova, R. M. Esayan, E. N. Andreeva, Z. A. Uzhegova, M. A. Kareva, N. Yu. Kalinchenko, B. M. Shifman, V. V. Fadeev, E. V. Biryukova, M. B. Antsiferov, L. A. Suplotova, T. P. Kiseleva, M. I. Yarmolinskaya, L. V. Suturina
Publikováno v:
Ожирение и метаболизм, Vol 18, Iss 3, Pp 345-382 (2021)
Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive diseases characterized by a defect in one of the enzymes or transport proteins involved in the cortisol synthesis in the adrenal cortex. The most common form of CAH, which occurs
Externí odkaz:
https://doaj.org/article/3369b7791129437fa976464c14c3294c
Akademický článek
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Akademický článek
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Publikováno v:
Андрология и генитальная хирургия, Vol 21, Iss 1, Pp 22-28 (2020)
Introduction. Single-stage feminization genitoplasty under the age of 12 months is recommended by the international consensus on the treatment of girls with congenital adrenal hyperplasia (CAH).The study objective is to evaluate the results of femini
Externí odkaz:
https://doaj.org/article/f250e4d72bda41d898e7d578b25bdaad
Clinical application experience of asfotase alfa for a young patient with childhood hypophosphatasia
Autor:
Nataliya Y. Kalinchenko, Olga O. Golounina, Tatiana A. Grebennikova, Galina A. Melnichenko, Anatoly N. Tiulpakov, Zhanna E. Belaya
Publikováno v:
Остеопороз и остеопатии, Vol 22, Iss 1, Pp 24-29 (2019)
Hypophosphatasia (HPP) is a rare hereditary metabolic disease characterized by defective bone and dental mineralization, systemic complications that lead to disability of patients. HPP is classified into six forms according to the age of onset and se
Externí odkaz:
https://doaj.org/article/31a314c6f93344f7a6c3c70210b0bfac