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pro vyhledávání: '"E G, Przhiialkovskaia"'
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:
Arkhiv patologii. 72(1)
Pituitary adenomas are benign, but 30-50% of patients do not achieve remission after treatment. The purpose of the study was to analyze the prognostic value of immunoexpression of the proliferation marker Ki-67 and the angiogenetic factors CD31 and V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4dfd3222503cb5d4453feef8b8bb9393
https://pubmed.ncbi.nlm.nih.gov/20369584
https://pubmed.ncbi.nlm.nih.gov/20369584