Zobrazeno 1 - 10
of 87
pro vyhledávání: '"multiple endocrine neoplasia syndrome"'
Publikováno v:
Waike lilun yu shijian, Vol 26, Iss 06, Pp 522-527 (2021)
Objective To investigate the association between RET genotype and disease phenotype in the patients with hereditary medullary thyroid carcinoma (HMTC). Methods A total of 13 patients diagnosed as HMTC and undergoing surgical treatment for thyroid car
Externí odkaz:
https://doaj.org/article/b527564f6f284edea548e1a9001b6fe1
Akademický článek
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Autor:
Pavel O. Rumiantsev, Konstantin Y. Slashchuk, Sergey V. Korenev, Andrei G. Goncharov, Dmitriy G. Beltsevich, Olga S. Chukhacheva
Publikováno v:
Эндокринная хирургия, Vol 13, Iss 3, Pp 105-117 (2020)
Medullary thyroid cancer (MTC) is about 5% of all thyroid carcinomas and is hereditary in 2030% of cases. Multiple endocrine neoplasia syndrome type 2 (MEN2), in addition to medullary thyroid cancer, may include pheochromocytoma, hyperparathyroidism,
Externí odkaz:
https://doaj.org/article/aec487359e2c46ddb52c96fc5048156c
Autor:
L. Ya. Rozhinskaya, P. M. Khandaeva, A. S. Lutsenko, A. M. Lapshina, A. Yu. Grigor'ev, S. D. Arapova, Zh. E. Belaya, G. A. Mel'nichenko
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 46, Iss 3, Pp 270-275 (2018)
Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer's syndrome) is a group of heterogeneous inherited diseases, with its pathogenesis related to hyperplasia or neoplasms of several endocrine glands. This syndrome is characterized by autosomal
Externí odkaz:
https://doaj.org/article/c68396e1228f4d548596762f98ef4976
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Эндокринная хирургия, Vol 7, Iss 4, Pp 4-13 (2013)
In the study were enrolled 137 patients with medullary thyroid cancer (MTC). Low 35%-sensitivity of FNAC and high accuracy of basal calcitonin in MTC diagnostics were found. Mutation analysis of the RET pro- tooncogene in familial and sporadic MTC, R
Externí odkaz:
https://doaj.org/article/0f5f1f5ae8934b5291667a7813712f5f
Autor:
D O Gazizova, D G Beltsevich
Publikováno v:
Эндокринная хирургия, Vol 7, Iss 3, Pp 4-21 (2013)
During last 4 years leading endocrine societies of the world published clinical recommendations on diag nostics and treatment of medullary thyroid cancer. The article covers most aspects of following patients with this pathology.
Externí odkaz:
https://doaj.org/article/9bf7642e5f774a4aa325fdbee303726e
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 6, Pp PD10-PD12 (2016)
With the increasing use of 18F-Fluro-Deoxyglucose (FDG) Positron Emission Tomography (PET) the number of thyroid incidentalomas is on the rise. Focal thyroid incidentalomas identified by FDG-PET have been reported to have a high incidence of maligna
Externí odkaz:
https://doaj.org/article/695bf432243b439383bd0b3affc8d360
Autor:
Andrei G. Goncharov, Olga S. Chukhacheva, Konstantin Y. Slashchuk, Sergey V. Korenev, D. G. Beltsevich, Pavel O. Rumiantsev
Publikováno v:
Эндокринная хирургия, Vol 13, Iss 3, Pp 105-117 (2020)
Medullary thyroid cancer (MTC) is about 5% of all thyroid carcinomas and is hereditary in 2030% of cases. Multiple endocrine neoplasia syndrome type 2 (MEN2), in addition to medullary thyroid cancer, may include pheochromocytoma, hyperparathyroidism,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dc4dd820b8677dc65bd5d62923b62af
https://surg-endojournals.ru/serg/article/viewFile/11270/pdf
https://surg-endojournals.ru/serg/article/viewFile/11270/pdf
Autor:
Patimat Khandaeva, Alexander Lutsenko, L Ya Rozhinskaya, S D Arapova, Zh E Belaya, A. M. Lapshina, Galina A. Melnichenko, A Yu Grigor'ev
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 46, Iss 3, Pp 270-275 (2018)
Multiple endocrine neoplasia syndrome type 1 (MEN1, Wermer's syndrome) is a group of heterogeneous inherited diseases, with its pathogenesis related to hyperplasia or neoplasms of several endocrine glands. This syndrome is characterized by autosomal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f106d21997df349c0bd0a48831855bf
https://doi.org/10.18786/2072-0505-2018-46-3-270-275
https://doi.org/10.18786/2072-0505-2018-46-3-270-275