Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Dmitry V. Kalinin"'
Autor:
Anastasiya V. Snezhkina, Vladislav S. Pavlov, Dmitry V. Kalinin, Elena A. Pudova, George S. Krasnov, Asiya F. Ayupova, Anastasiya A. Kobelyatskaya, Alexey A. Dmitriev, Dmitrii A. Atiakshin, Maria S. Fedorova, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Vagal paraganglioma (VPGL) is a rare neuroendocrine tumor that originates from the paraganglion associated with the vagus nerve. VPGLs present challenges in terms of diagnostics and treatment. VPGL can occur as a hereditary tumor and, like other head
Externí odkaz:
https://doaj.org/article/832d98b91b964158b2ed1e1c2b7796ad
Autor:
Elena A. Pudova, Anastasiya A. Kobelyatskaya, Irina V. Katunina, Anastasiya V. Snezhkina, Maria S. Fedorova, Vladislav S. Pavlov, Ildar R. Bakhtogarimov, Margarita S. Lantsova, Sergey P. Kokin, Kirill M. Nyushko, Boris Ya. Alekseev, Dmitry V. Kalinin, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2418 (2023)
Radical prostatectomy is the gold standard treatment for prostate cancer (PCa); however, it does not always completely cure PCa, and patients often experience a recurrence of the disease. In addition, the clinical and pathological parameters used to
Externí odkaz:
https://doaj.org/article/1465453d633e432487d72a18b320472c
Autor:
Oleg V. Zayratyants, Maria V. Samsonova, Andrey L. Cherniaev, Oleko D. Mishnev, Liudmila M. Mikhaleva, Nikolai M. Krupnov, Dmitry V. Kalinin
Publikováno v:
Судебная Медицина, Vol 6, Iss 4, Pp 10-23 (2020)
Background: Pathological anatomy, patogenesis and the morphogenesis of manifestations and complications of COVID-19 remain insufficiently studied. The fullest information on structural bases of organs and tissues alterations by new coronavirus diseas
Externí odkaz:
https://doaj.org/article/9455dce95c4f4da4a80c1afa7b9a088c
Autor:
Anna V. Kudryavtseva, Dmitry V. Kalinin, Vladislav S. Pavlov, Maria V. Savvateeva, Maria S. Fedorova, Elena A. Pudova, Anastasiya A. Kobelyatskaya, Alexander L. Golovyuk, Zulfiya G. Guvatova, George S. Razmakhaev, Tatiana B. Demidova, Sergey A. Simanovsky, Elena N. Slavnova, Andrey А. Poloznikov, Andrey P. Polyakov, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Krasnov, Anastasiya V. Snezhkina
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-11 (2020)
Abstract Background Vagal paragangliomas (VPGLs) belong to a group of rare head and neck neuroendocrine tumors. VPGLs arise from the vagus nerve and are less common than carotid paragangliomas. Both diagnostics and therapy of the tumors raise signifi
Externí odkaz:
https://doaj.org/article/d3d667cb88dc4d0782b8c0c21e300aac
Autor:
Vladislav S. Pavlov, Dmitry V. Kalinin, Elena N. Lukyanova, Alexander L. Golovyuk, Maria S. Fedorova, Elena A. Pudova, Maria V. Savvateeva, Anastasiya V. Lipatova, Zulfiya G. Guvatova, Andrey D. Kaprin, Marina V. Kiseleva, Tatiana B. Demidova, Sergey A. Simanovsky, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Krasnov, Anastasiya V. Snezhkina, Anna V. Kudryavtseva
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-6 (2020)
Abstract Background Carotid and vagal paragangliomas (CPGLs and VPGLs) are rare neoplasms that arise from the paraganglia located at the bifurcation of carotid arteries and vagal trunk, respectively. Both tumors can occur jointly as multiple paragang
Externí odkaz:
https://doaj.org/article/40962aa040a7464bab83b50d630f1b24
Autor:
Anastasiya A. Kobelyatskaya, Alexander A. Kudryavtsev, Anna V. Kudryavtseva, Anastasiya V. Snezhkina, Maria S. Fedorova, Dmitry V. Kalinin, Vladislav S. Pavlov, Zulfiya G. Guvatova, Pavel A. Naberezhnev, Kirill M. Nyushko, Boris Y. Alekseev, George S. Krasnov, Elizaveta V. Bulavkina, Elena A. Pudova
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 19, p 11695 (2022)
Following radical surgery, patients may suffer a relapse. It is important to identify such patients so that therapy tactics can be modified appropriately. Existing stratification schemes do not display the probability of recurrence with enough precis
Externí odkaz:
https://doaj.org/article/6d1be706ca49440dbf01d48203ac229f
Autor:
Anastasiya V. Snezhkina, Elena N. Lukyanova, Andrew R. Zaretsky, Dmitry V. Kalinin, Anatoly V. Pokrovsky, Alexander L. Golovyuk, George S. Krasnov, Maria S. Fedorova, Elena A. Pudova, Sergey L. Kharitonov, Nataliya V. Melnikova, Boris Y. Alekseev, Marina V. Kiseleva, Andrey D. Kaprin, Alexey A. Dmitriev, Anna V. Kudryavtseva
Publikováno v:
BMC Medical Genetics, Vol 20, Iss S1, Pp 5-13 (2019)
Abstract Background Carotid paragangliomas (CPGLs) are rare neuroendocrine tumors that arise from the paraganglion at the bifurcation of the carotid artery and are responsible for approximately 65% of all head and neck paragangliomas. CPGLs can occur
Externí odkaz:
https://doaj.org/article/2105a401902e4c3ab6c7f1fa82bc4cf2
Autor:
Anna V. Kudryavtseva, Elena N. Lukyanova, Dmitry V. Kalinin, Andrew R. Zaretsky, Anatoly V. Pokrovsky, Alexander L. Golovyuk, Maria S. Fedorova, Elena A. Pudova, Sergey L. Kharitonov, Vladislav S. Pavlov, Anastasiya A. Kobelyatskaya, Nataliya V. Melnikova, Alexey A. Dmitriev, Andrey P. Polyakov, Boris Y. Alekseev, Marina V. Kiseleva, Andrey D. Kaprin, George S. Krasnov, Anastasiya V. Snezhkina
Publikováno v:
BMC Medical Genomics, Vol 12, Iss S2, Pp 23-34 (2019)
Abstract Background Carotid body tumor (CBT) is a rare neoplasm arising from paraganglion located near the bifurcation of the carotid artery. There is great intra-tumor heterogeneity, and CBT development could be associated with both germline and som
Externí odkaz:
https://doaj.org/article/2e9b4e602b0c4156b0100670e6045ff3
Autor:
Anastasiya V. Snezhkina, Maria S. Fedorova, Vladislav S. Pavlov, Dmitry V. Kalinin, Alexander L. Golovyuk, Elena A. Pudova, Zulfiya G. Guvatova, Nataliya V. Melnikova, Alexey A. Dmitriev, George S. Razmakhaev, Andrey A. Poloznikov, Galina S. Alekseeva, Andrey D. Kaprin, George S. Krasnov, Anna V. Kudryavtseva
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Head and neck paragangliomas (HNPGLs) are rare neuroendocrine tumors that have a high degree of heritability and are predominantly associated with mutations in ten genes, such as SDHx, SDHAF2, VHL, RET, NF1, TMEM127, MAX, FH, MEN2, and SLC25A11. Eluc
Externí odkaz:
https://doaj.org/article/0984d7b56b80408e99976452d1ef8d8b
Autor:
Anastasiya V. Snezhkina, Elena N. Lukyanova, Dmitry V. Kalinin, Anatoly V. Pokrovsky, Alexey A. Dmitriev, Nadezhda V. Koroban, Elena A. Pudova, Maria S. Fedorova, Nadezhda N. Volchenko, Oleg A. Stepanov, Ekaterina A. Zhevelyuk, Sergey L. Kharitonov, Anastasiya V. Lipatova, Ivan S. Abramov, Alexander V. Golovyuk, Yegor E. Yegorov, Khava S. Vishnyakova, Alexey A. Moskalev, George S. Krasnov, Nataliya V. Melnikova, Dmitry S. Shcherbo, Marina V. Kiseleva, Andrey D. Kaprin, Boris Y. Alekseev, Andrew R. Zaretsky, Anna V. Kudryavtseva
Publikováno v:
BMC Medical Genomics, Vol 11, Iss S1, Pp 5-19 (2018)
Abstract Background Carotid body tumor (CBT) is a form of head and neck paragangliomas (HNPGLs) arising at the bifurcation of carotid arteries. Paragangliomas are commonly associated with germline and somatic mutations involving at least one of more
Externí odkaz:
https://doaj.org/article/3bad409c00ff45b99812fa4c6066a2b2