Search Results - "Khairieva, A V"

Fulminant hypercorticism due to ACTG producing pheochromocytoma by Useinova, Z. T., Pigarova, E. A., Bel’tsevich, D. G., Chevais, A., Dzeranova, L. K., Sitkin, I. I., Tarbaeva, N. V., Khairieva, A. V., Degtyarev, M. V., Platonova, N. M., Troshina, E. A., Bondarenko, E. V.

“…Endogenous hypercorticism (EH) is a severe symptom complex caused by hypercortisolemia; according to the etiology, ACTH-dependent and ACTH-independent variants…”
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Severe bone complications of primary hyperparathyroidism in a young patient with the rare verified mutation of MEN1 by Eremkina, A. K., Sazonova, D. V., Bibik, E. E., Sheikhova, A. Z., Khairieva, A. V., Buklemishev, Yu. V., Mokrysheva, N. G.

“…Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine…”
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A clinical case of phosphopenic osteomalacia due to paraneoplastic secretion of metastatic prostate cance by Gronskaya, S. A., Golounina, O. O., Buklemishev, Yu. V., Khairieva, A. V., Degtyarev, M. V., Rozhinskaya, L. Ya, Belaya, Zh. E.

“…Phosphaturic mesenchymal tumor can cause osteomalacia due to excessive secretion of fibroblast growth factor 23 (FGF23), which disrupts the metabolism of…”
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Features of diagnosis and treatment of fulminant hypercorticism due to ACTH-producing pheochromocytoma: a clinical case by Ebanoidze, L. G., Pigarova, E. A., Beltsevich, D. G., Sheva, A., Dzeranova, L. K., Sitkin, I. I., Tarbaeva, N. V., Khairieva, A. V., Degtyarev, M. V., Bondarenko, E. V.

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Fulminant hypercorticism due to ACTG producing pheochromocytoma by Useinova, Z T, Pigarova, E A, Bel'tsevich, D G, Chevais, A, Dzeranova, L K, Sitkin, I I, Tarbaeva, N V, Khairieva, A V, Degtyarev, M V, Platonova, N M, Troshina, E A, Bondarenko, E V

“…Endogenous hypercorticism (EH) is a severe symptom complex caused by hypercortisolemia; according to the etiology, ACTH-dependent and ACTH-independent variants…”
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Severe bone complications of primary hyperparathyroidism in a young patient with the rare verified mutation of MEN1 by Eremkina, A K, Sazonova, D V, Bibik, E E, Sheikhova, A Z, Khairieva, A V, Buklemishev, Yu V, Mokrysheva, N G

“…Multiple endocrine neoplasia type 1 syndrome (MEN1) is a rare inherited disorder that can include combinations of more than 20 endocrine and non-endocrine…”
Get more information