Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ștefania Dorobanțu"'
Autor:
Andreea Teodora Constantin, Ioana Streata, Mirela Silvia Covăcescu, Anca Lelia Riza, Ioana Roșca, Corina Delia, Lucia Maria Tudor, Ștefania Dorobanțu, Adina Dragoș, Diana Ristea, Mihai Ioana, Ioan Gherghina
Publikováno v:
Diagnostics, Vol 13, Iss 12, p 1988 (2023)
Familial hypercholesterolemia (FH) is a genetic disease marked by high levels of LDL-cholesterol. This condition has long-term clinical implications, such as cardiovascular events, that are evident during adult life. Here, we report on a single-cente
Externí odkaz:
https://doaj.org/article/6e0c07a7745c430d871fc88b3e9ddc87
Autor:
Gabriela Popescu-Hobeanu, Anca-Lelia Riza, Ioana Streață, Ștefania Tudorache, Alexandru Comănescu, Florentina Tănase, Roxana Cristina Drăgușin, Cornelia Pascu, Anda Lorena Dijmărescu, Monica-Laura Cara, Ștefania Dorobanțu, Bianca Petre-Mandache, Mihai Cucu, Simona Serban Sosoi, Mihai Ioana, Dominic Iliescu, Florin Burada
Publikováno v:
Genes, Vol 13, Iss 12, p 2246 (2022)
It is well known that first-trimester miscarriages are associated with chromosome abnormalities, with numerical chromosome abnormalities being the ones most commonly detected. Conventional karyotyping is still considered the gold standard in the anal
Externí odkaz:
https://doaj.org/article/35f1bbc7851342cea95b8c89ce49767a
Autor:
Gherghina, Andreea Teodora Constantin, Ioana Streata, Mirela Silvia Covăcescu, Anca Lelia Riza, Ioana Roșca, Corina Delia, Lucia Maria Tudor, Ștefania Dorobanțu, Adina Dragoș, Diana Ristea, Mihai Ioana, Ioan
Publikováno v:
Diagnostics; Volume 13; Issue 12; Pages: 1988
Familial hypercholesterolemia (FH) is a genetic disease marked by high levels of LDL-cholesterol. This condition has long-term clinical implications, such as cardiovascular events, that are evident during adult life. Here, we report on a single-cente
Autor:
Francisc Mixich, Marian Olaru, Mihai G. Netea, Elena Leocadia Popescu, Adela Ciocoiu, Ileana Băzăvan, Alina Liliana Cimpoeru, Andreea Nicoleta Ștefan, Răzvan Mihail Pleșea, Andreea Anghel, Mimi Nițu, Marius Sorin Ciontea, Anca Riza, Mihai Olteanu, Mihai Gabriel Cucu, Tiberiu Tătaru, Florin Burada, Reinout van Crevel, Simona Șerban-Șoșoi, Iulia Căpitănescu, Ioana Streața, Mihai Ioana, Aida Maria Stroe, Ștefania Dorobanțu, Ramona Cioboata
Publikováno v:
Revista Romana de Medicina de Laborator, 25, 47-53
Romanian Journal of Laboratory Medicine, Vol 25, Iss 1, Pp 47-53 (2017)
Revista Romana de Medicina de Laborator, 25, 1, pp. 47-53
Romanian Journal of Laboratory Medicine, Vol 25, Iss 1, Pp 47-53 (2017)
Revista Romana de Medicina de Laborator, 25, 1, pp. 47-53
Autophagy, a homeostatic process involved in nutrient regeneration and immune responses, may be involved in intracellular killing of M. tuberculosis. Several studies linked variation in autophagy genes with susceptibility to pulmonary tuberculosis, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a01ec194385d94e46a06110a4f492b28
https://doi.org/10.1515/rrlm-2017-0002
https://doi.org/10.1515/rrlm-2017-0002
Autor:
Isis Ricaño-Ponce, Anca-Lelia Riza, Aline H. de Nooijer, Andrei Pirvu, Stefania Dorobantu, Adina Dragos, Ioana Streata, Mihaela Roskanovic, Inge Grondman, Florentina Dumitrescu, Vinod Kumar, Mihai G. Netea, Mihai Ioana
Publikováno v:
BMC Infectious Diseases, Vol 22, Iss 1, Pp 1-10 (2022)
Abstract Background Sepsis is a heterogeneous syndrome due to a variable range of dysregulated processes in the host immune response. Efforts are made to stratify patients for personalized immune-based treatments and better prognostic prediction. Usi
Externí odkaz:
https://doaj.org/article/e35b5260318e4705ba0bb7cb36dad0a1
Autor:
Anca-Lelia Riza, Ioana Streață, Eugenia Roza, Magdalena Budișteanu, Catrinel Iliescu, Carmen Burloiu, Mihaela-Amelia Dobrescu, Stefania Dorobanțu, Adina Dragoș, Andra Grigorescu, Tiberiu Tătaru, Mihai Ioana, Raluca Teleanu
Publikováno v:
Genes, Vol 13, Iss 7, p 1253 (2022)
Early-onset developmental epileptic encephalopathy (DEE) refers to an age-specific, diverse group of epilepsy syndromes with electroclinical anomalies that are associated with severe cognitive, behavioral, and developmental impairments. Genetic DEEs
Externí odkaz:
https://doaj.org/article/207c4a9d838447c896cb8c50f4e428fc