Zobrazeno 1 - 7
of 7
pro vyhledávání: '"E. P. Vasilyev"'
Autor:
Yu. V. Tikhonovich, L. G. Chernich, I. N. Velikanov, V. M. Polyakova, E. V. Vasilyev, V. M. Petrov, E. V. Shreder, Е. V. Glavatskich, A. N. Tyulpakov
Publikováno v:
Сахарный диабет, Vol 25, Iss 1, Pp 81-88 (2022)
Mutations in the GLIS3 gene encoding the GLIS3 transcription factor are cause of a rare syndromic form of neonatal diabetes mellitus (NDM) with congenital hypothyroidism. Additional features include congenital glaucoma, hepatic fibrosis, polycystic k
Externí odkaz:
https://doaj.org/article/15276206fcaa42249961e40a5ce1fb10
Autor:
M. Yu. Yukina, V. R. Mustafina, E. V. Vasilyev, E. A. Troshina, N. M. Platonova, D. G. Beltsevich
Publikováno v:
Медицинский совет, Vol 0, Iss 7, Pp 150-154 (2021)
Pheochromocytoma/paraganglioma is a neuroendocrine tumor of chromaffin and nonchromaffin cells of the autonomic nervous system, in most cases localized in the medullary layer of the adrenal gland. Its development is often associated with genetic pred
Externí odkaz:
https://doaj.org/article/64d9aa005006432183cb570b2bee2f6c
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
Publikováno v:
Neftyanoe khozyaystvo - Oil Industry. 1:60-65
Autor:
E. P. Vasilyev
Publikováno v:
Vestnik of Ryazan State Radio Engineering University. 73:26-36
Autor:
E. P. Vasilyev
Publikováno v:
Vestnik of Ryazan State Radio Engineering University. 72:62-70
Autor:
E. P. Vasilyev
Publikováno v:
Vestnik of Ryazan State Radio Engineering University. 71:23-33