Zobrazeno 1 - 10
of 527
pro vyhledávání: '"molecular genetic testing"'
Autor:
K. K. Laktionov, K. A. Sarantseva, L. A. Nelyubina, S. V. Gamayunov, E. A. Kolesnikova, M. G. Gordiev
Publikováno v:
Сибирский онкологический журнал, Vol 23, Iss 2, Pp 72-81 (2024)
Lung cancer remains one of the most dangerous and most common cancers, requiring constant improvement of diagnostic and treatment methods. The genetic heterogeneity of lung cancer forces us to search for new therapeutic targets in an attempt to achie
Externí odkaz:
https://doaj.org/article/73b447e88d214b60aa826941c8d2573c
Autor:
A. A. Rogozhina, A. O. Averkova, E. A. Zubova, L. O. Minushkina, V. A. Brazhnik, O. N. Ivanova, M. A. Chichkova, N. R. Khasanov, E. D. Kosmacheva, O. I. Boeva, D. A. Zateyshchikov
Publikováno v:
Российский кардиологический журнал, Vol 28, Iss 10 (2023)
Aim. To assess the possibility of familial hypercholesterolemia (FH) detection among patients with early coronary artery disease (CAD) in practice in comparison with data from different populations. Patients with early manifestations of CAD are a pro
Externí odkaz:
https://doaj.org/article/f41139a48f6a4da18bfe7de9ad6a3c87
Publikováno v:
Clinical Ophthalmology, Vol Volume 16, Pp 239-244 (2022)
Alexandre Lachance,1,2 Mélanie Hébert,1,2 Marc Hébert,1– 3 Christian Salesse,1,2 Serge Bourgault,1,2 Ali Dirani1,2 1Faculté de médecine, Université Laval, Québec, QC, Canada; 2Département d’ophtalmologie et d’oto-rhino-laryngologie –
Externí odkaz:
https://doaj.org/article/b5f60da44ae845f392242af26d3a5cf7
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 65, Iss 5, Pp 259-270 (2022)
Muscular dystrophies are a clinically and genetically heterogeneous group of disorders involving the skeletal muscles. They have a progressive clinical course and are characterized by muscle fiber degeneration. Congenital muscular dystrophies (CMD) i
Externí odkaz:
https://doaj.org/article/2acf9fb043874c1ca73d3ab5ce3de26d
Autor:
Anastasia V. Blokhina, Alexandra I. Ershova, Alexey N. Meshkov, Anna V. Kiseleva, Marina V. Klimushina, Anastasia A. Zharikova, Evgeniia A. Sotnikova, Vasily E. Ramensky, Oxana M. Drapkina
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
One of the most common autosomal dominant disorders is familial hypercholesterolemia (FH), causing premature atherosclerotic cardiovascular diseases and a high risk of death due to lifelong exposure to elevated low-density lipoprotein cholesterol (LD
Externí odkaz:
https://doaj.org/article/b2d0004e163a4fe693bff5c150365aa7
Autor:
Yi Ding, Guoli Chen
Publikováno v:
Human Pathology Reports, Vol 28, Iss , Pp 300632- (2022)
Mainly driven by the clinical need, molecular genetic testing has been integrated into the standard patient care of cancer management including colorectal cancer (CRC) for various clinical purposes. A proper selection of anti-cancer therapies relies
Externí odkaz:
https://doaj.org/article/61b9f90640f04be594887a9bf3b76341
Autor:
Nikolay N. Murashkin, Alexander I. Materikin, Eduard T. Ambarchian, Roman V. Epishev, Leonid A. Opryatin, Roman A. Ivanov, Daria S. Kukoleva, Daria G. Kuptsova, Alexander A. Pushkov, Marina Yu. Pomazanova, Yana V. Kozyr
Publikováno v:
Вопросы современной педиатрии, Vol 19, Iss 6, Pp 483-489 (2020)
Background. Nowadays, dermatoses with mixed clinical picture and resistant to classical management become more common. The presence of various genetic disorders typical for most chronic dermatoses may indicate possible combination of several nosologi
Externí odkaz:
https://doaj.org/article/b30554053689421a99f4a299896af686
Autor:
Aleksandr V. Alimov, Svetlana S. Smirnova, Evgenia V. Lelenkova, Aleksandr Yu. Markaryan, Ivan V. Vyalykh, Vladislav K. Verevshchikov, Andrey B. Komissarov, Anna A. Sominina
Publikováno v:
Журнал микробиологии, эпидемиологии и иммунобиологии, Vol 97, Iss 2, Pp 140-149 (2020)
Objective. To study the role of influenza viruses in the development of severe acute respiratory infections (SARI) in patients admitted to Yekaterinburg hospitals during 2017-2018 epidemic season.Materials and Methods. A retrospective epidemiological
Externí odkaz:
https://doaj.org/article/f4d4ceb31bec46e49eb5fcf6063a44b0
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:
Frontiers in Molecular Biosciences, Vol 8 (2021)
Background: The lifespan of Marfan Syndrome (MFS) patients is shortened, especially in patients without early diagnostics, preventive treatment, and elective surgery. Clinically, MFS diagnosis is mainly dependent on phenotypes, but for children, spor
Externí odkaz:
https://doaj.org/article/40d2dcdca2a44ffdb42581f73498598c