Zobrazeno 1 - 10
of 93
pro vyhledávání: '"E A PIGAROVA"'
Publikováno v:
Терапевтический архив, Vol 90, Iss 10, Pp 115-127 (2018)
A high prevalence of vitamin D deficiency and its negative consequences for health is identified as area of primary concern for scientists and clinicians worldwide. Vitamin D deficiency affects not only bone health but many socially significant acute
Externí odkaz:
https://doaj.org/article/a619f669953440ce93dc1f954e3f2f58
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:
S Yu Vorotnikova, E A Pigarova
Publikováno v:
Остеопороз и остеопатии, Vol 19, Iss 3, Pp 23-27 (2016)
The data from a number of clinical trials investigating a once-yearly infusion of5 mg zoledronic acidshow a marked efficacy of this intervention in the treatment of primary and secondary osteoporosis with a combination of fracture risk reduction and
Externí odkaz:
https://doaj.org/article/3765946a1cdb49fbb715fcd71cdbeb3e
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:
E A Pigarova
Publikováno v:
Остеопороз и остеопатии, Vol 18, Iss 2, Pp 29-32 (2015)
Vitamin D belongs to the group of fat-soluble vitamins. It is naturally present in only a very limited amount of food, and the synthesis in the human body is possible only under certain conditions - when the UV rays of sunlight fall on the skin. Nati
Externí odkaz:
https://doaj.org/article/54270711ba0d4340bf4a08f320a8ae1c
Publikováno v:
Остеопороз и остеопатии, Vol 18, Iss 3, Pp 36-39 (2015)
Clinical symptoms of vitamin D deficiency may be quite misleading and masked as rare hereditary syndromes. We describe a family, sister and brother presented with the pain in lower extremities at the age of 14 and 16years accordingly, with severe vit
Externí odkaz:
https://doaj.org/article/75c188dcadf54102b06b8b7fb0877d49
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 A PIGAROVA, L Ya ROZhINSKAYa
Publikováno v:
Остеопороз и остеопатии, Vol 17, Iss 1, Pp 33-37 (2014)
Переломы при остеопорозе представляют собой крайне неблагоприятное осложнение заболевания, и нередко могут иметь, и что особенно ярко
Externí odkaz:
https://doaj.org/article/8800e96fda5f4d6bac82814f7c0dfb99
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
Publikováno v:
Ожирение и метаболизм, Vol 21, Iss 2, Pp 188-194 (2024)
Hyperprolactinemia has multiple etiologies and is the most common endocrine manifestation of pathology of the hypothalamic-pituitary axis. Hyperprolactinemic hypogonadism is of great scientific interest due to the prevalence of endocrine pathology
Externí odkaz:
https://doaj.org/article/0468d0d5de364197aa4795f726bf3094