Zobrazeno 1 - 10
of 10
pro vyhledávání: '"E O Mamedova"'
Autor:
G A Melnichenko, Zh E Belaya, L Ya Rozhinskaya, T A Grebennikova, E A Pigarova, N V Toroptsova, O A Nikitinskaya, L Ya Farba, N V Tarbaeva, T O Chernova, L K Dzeranova, A V Ilyin, S V Yureneva, I V Kryukova, E O Mamedova, E V Biryukova, N V Zagorodny, S S Rodionova, O M Lesniak, I A Skripnikova, A V Dreval, L A Alekseeva, I I Dedov
Publikováno v:
Остеопороз и остеопатии, Vol 19, Iss 3, Pp 28-36 (2016)
Представлено краткое изложение клинических рекомендаций по диагностике и лечению остеопороза, разработанных членами Российской ассоц
Externí odkaz:
https://doaj.org/article/2ac7af4c0af84749a3f1bafb51d43098
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
Autor:
N G Mokrysheva, E O Mamedova, E A Pigarova, Yu A Berezkina, A V Vorontsov, V N Azizyan, A Yu Grigoriev, T R Alekseeva, M A Kutin, A V Kochatkov, L Ya Rozhinskaya
Publikováno v:
Терапевтический архив, Vol 87, Iss 12, Pp 122-127 (2015)
The article briefly reviews the specific features of target-organ lesions in multiple endocrine neoplasia type 1 (MEN1) syndrome and a clinical case of genetically confirmed MEN1 syndrome in a young female patient. Despite the relative rarity of this
Externí odkaz:
https://doaj.org/article/1b1030c2700b4082a8a429ef6f1b5c51
Autor:
E O Mamedova, N G Mokrysheva, E G Przhiialkovskaia, E A Pigarova, L Ia Rozhinskaia, A N Tiul'pakov
Publikováno v:
Терапевтический архив, Vol 86, Iss 10, Pp 87-91 (2014)
Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant hereditary disease due to a mutation in the MEN1 tumor suppressor gene. The risk of the disease in first-degree relatives of MEN1 mutation carriers is 50%. MEN1 gene mutations ar
Externí odkaz:
https://doaj.org/article/45bd109a6f2d41909215694b048c052a
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 1, Pp 79-84 (2024)
Multiple endocrine neoplasia type 1 (MEN1) and congenital adrenal hyperplasia (CAH) are rare monogenic hereditary endocrinopathies with a prevalence of 1–9 cases per 100,000 and 9–15 cases per 100,000, respectively. MEN1 is characterized by the d
Externí odkaz:
https://doaj.org/article/a93e058ef6eb428ebd6ca51daf7e3cba
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 170-171 (2024)
A corrigendum on "A Rare Case of Co-occurrence of Multiple Endocrine Neoplasia Syndrome and Congenital Adrenal Hyperplasia" by Axenia S. Bondarenko, Elizaveta O. Mamedova, Zhanna E. Belaya, Galina A. Melnichenko (2024). Obesity and metabolism. 2024
Externí odkaz:
https://doaj.org/article/5b6d928c9c874ef399c03ab254734a0f
Publikováno v:
Problems of Endocrinology. 69:24-30
Functioning pituitary adenomas and pheochromocytomas/paragangliomas are rare in the general population. Pituitary adenomas occur in the familial setting in approximately 5% of cases, whereas pheochromocytomas/paragangliomas can be hereditary in 30–
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c53b1fe51cb12da6289a5690df63e5ab
https://doi.org/10.14341/probl13196
https://doi.org/10.14341/probl13196
Autor:
I. I. Dedov, G. A. Melnichenko, N. G. Mokrysheva, E. N. Andreeva, M. B. Antsiferov, D. G. Beltsevich, E. E. Bibik, A. M. Gorbacheva, M. V. Degtyarev, L. V. Yeghshatyan, A. K. Eremkina, T. L. Karonova, I. V. Kim, J. A. Krupinova, I. V. Kryukova, N. S. Kuznetsov, S. V. Lukyanov, E. O. Mamedova, N. V. Markina, S. S. Mirnaya, E. A. Pigarova, L. Ya. Rozhinskaya, K. Yu. Slashchuk, I. V. Sleptsov, N. B. Chagai
Publikováno v:
Endocrine Surgery. 16:5-54
The article presents a draft of clinical recommendations for the diagnosis and treatment of primary hyperparathyroidism in adult patients, which provides a modern examination algorithm, discusses the basic principles of laboratory, instrumental diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1024e1f3d249eadb44f2084ef85d2b5a
https://doi.org/10.14341/serg12790
https://doi.org/10.14341/serg12790
Autor:
D. A. Trukhina, E. O. Mamedova, A. M. Lapshina, E. V. Vasilyev, A. N. Tiulpakov, Zh. E. Belaya
Publikováno v:
Problemy endokrinologii. 67(6)
BACKGROUND: Multiple endocrine neoplasia type 1 (MEN 1) is a rare autosomal dominant disorder caused by mutations in the MEN1 gene, which encodes the menin protein. If a patient has the MEN 1 phenotype in the absence of mutations in the MEN1 gene, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b0ccd56094ad16d3b97e8337d607cff
https://pubmed.ncbi.nlm.nih.gov/35018761
https://pubmed.ncbi.nlm.nih.gov/35018761