Zobrazeno 1 - 7
of 7
pro vyhledávání: '"M Kh Toboeva"'
Publikováno v:
Терапевтический архив, Vol 91, Iss 2, Pp 97-100 (2019)
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often phenotypically similar to a weakened form of familial adenomatous polyposis. For the development of the disease mutations in both alleles
Externí odkaz:
https://doaj.org/article/bf83a884fa0044c380d4014c9e1d20fc
Autor:
A. S. Tsukanov, V. P. Shubin, A. M. Kuzminov, M. Kh. Toboeva, T. A. Savelyeva, V. N. Kashnikov, Yu. A. Shelygin
Publikováno v:
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, Vol 28, Iss 6, Pp 51-57 (2019)
Aim. In this research, we aim to develop a criterion for differentiating MutYH-associated polyposis from sporadic colon polyps.Materials and methods. A search for mutations in the MutYH gene was carried out using the PCR, electrophoresis and direct s
Externí odkaz:
https://doaj.org/article/c8232751b7824c77ab0a4b2fc8ea7eca
Autor:
M. Kh. Toboeva, Yu. A. Shelygin, A. S. Tsukanov, D. Yu. Pikunov, S. A. Frolov, A. A. Ponomarenko
Publikováno v:
Koloproktologia. 21:120-129
BACKGROUND: to date, there are no clear guidelines for MutYH-associated polyposis (MAP) surgery.AIM: to study the world literature on MutYH-associated polyposis surgery using a meta-analysis.MATERIALS AND METHODS: the systematic review was carried ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea263c3d276353d29b964d2e3ffc42c4
https://doi.org/10.33878/2073-7556-2022-21-4-120-129
https://doi.org/10.33878/2073-7556-2022-21-4-120-129
Publikováno v:
Alʹmanah Kliničeskoj Mediciny, Vol 46, Iss 1, Pp 16-22 (2018)
Up to 10% of cases of sporadic colorectal cancer are considered to be related to hereditary genetic factors. The rates of colorectal cancer related to already identified genetic factors is about 5%. In the last decades, due to the development of comp
Externí odkaz:
https://doaj.org/article/f66fd2e37f2442fe98c46b299ad271c1
Autor:
D. Yu. Pikunov, A. N. Loginova, A. M. Kuzminov, M. Kh. Toboeva, A. A. Barinov, A. S. Tsukanov
Publikováno v:
Koloproktologia. 21:25-33
Aim: based on literature data and our own experience, to demonstrate the need for a meticulous family history harvesting in patients with suspected hereditary polyposis syndrome, as well as the importance of conducting a complex molecular genetic stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::357aa51657e3102d7cd6e66dc5c06514
https://doi.org/10.33878/2073-7556-2022-21-2-25-33
https://doi.org/10.33878/2073-7556-2022-21-2-25-33
Publikováno v:
Терапевтический архив, Vol 91, Iss 2, Pp 97-100 (2019)
MutYH-associated polyposis is the only polyposis syndrome with an autosomal recessive type of inheritance, often phenotypically similar to a weakened form of familial adenomatous polyposis. For the development of the disease mutations in both alleles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d08705121960416576121ae943f2a798
https://ter-arkhiv.ru/0040-3660/article/viewFile/32958/pdf
https://ter-arkhiv.ru/0040-3660/article/viewFile/32958/pdf
Autor:
A. S. Tsukanov, A. M. Kuzminov, A V Gavryushin, D. V. Vyshegorodtsev, O A Maynovskaya, M Kh Toboeva, V Yu Korolik
Publikováno v:
Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko. 83(6)
Turcot syndrome is a rare hereditary syndrome characterized by a combination of brain tumors and colorectal cancer. According to the literature, about 150 such cases have been reported. This article presents a rare clinical case and a literature revi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a31bc0ed78b6869d6ed3c64cd6855de
https://pubmed.ncbi.nlm.nih.gov/32031170
https://pubmed.ncbi.nlm.nih.gov/32031170