Zobrazeno 1 - 4
of 4
pro vyhledávání: '"A V Khairieva"'
Autor:
S. A. Gronskaya, O. O. Golounina, Yu. V. Buklemishev, A. V. Khairieva, M. V. Degtyarev, L. Ya. Rozhinskaya, Zh. E. Belaya
Publikováno v:
Osteoporosis and Bone Diseases. 25:43-51
Phosphaturic mesenchymal tumor can cause osteomalacia due to excessive secretion of fibroblast growth factor 23 (FGF23), which disrupts the metabolism of phosphate and vitamin D. These tumors are predominantly benign, but less than 5% of them are mal
Autor:
A. K. Eremkina, D. V. Sazonova, E. E. Bibik, A. Z. Sheikhova, A. V. Khairieva, Yu. V. Buklemishev, N. G. Mokrysheva
Publikováno v:
Problems of Endocrinology. 68:81-93
Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine tumors. Unfortunately, none of the described MEN1 mutations has been associated with a peculiar
Autor:
A K, Eremkina, D V, Sazonova, E E, Bibik, A Z, Sheikhova, A V, Khairieva, Yu V, Buklemishev, N G, Mokrysheva
Publikováno v:
Problemy endokrinologii. 68(1)
Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine tumors. Unfortunately, none of the described MEN1 mutations has been associated with a peculiar
Publikováno v:
Khirurgiya. Zhurnal im. N.I. Pirogova. :36
To define the indications for pancreatoduodenectomy using 3D CT-imaging, to calculate the volume of damaged and intact tissues and to determine type of surgery depending on severity of disease in case of ductal pancreatic adenocarcinoma.Retrospective