Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Mihaela Dragomir"'
Autor:
Andra Grigore, Mihaela Dragomir, Onda-Tabita Călugăru, Dumitru Jardan, Cerasela Jardan, Melen Brînză, Paul Bălănescu, Daniel Coriu
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 15, p 8366 (2024)
Hemophilia A (HA) is an X-linked recessive bleeding disorder caused by mutations in the F8 gene, resulting in deficient or dysfunctional factor VIII (FVIII). This study aimed to characterize the mutational profile of HA in Romanian patients using nex
Externí odkaz:
https://doaj.org/article/88c2cd00c03143f8b7d22202038e48ac
Autor:
Mihaela Dragomir, Onda-Tabita Călugăru, Bogdan Popescu, Cerasela Jardan, Dumitru Jardan, Monica Popescu, Silvia Aposteanu, Sorina Bădeliță, Gabriela Nedelcu, Cătălin Șerban, Codruța Popa, Tatiana Vassu-Dimov, Daniel Coriu
Publikováno v:
Cancers, Vol 16, Iss 2, p 358 (2024)
Multiple myeloma is a hematologic neoplasm caused by abnormal proliferation of plasma cells. Sequencing studies suggest that plasma cell disorders are caused by both cytogenetic abnormalities and oncogene mutations. Therefore, it is necessary to dete
Externí odkaz:
https://doaj.org/article/6915b1c628934c0abfd89008c3da18a4
Autor:
Melen Brinza, Andra Grigore, Mihaela Dragomir, Dumitru Jardan, Cerasela Jardan, Paul Balanescu, Claudia Cristina Tarniceriu, Oana Viola Badulescu, Cristina Blag, Ciprian Tomuleasa, Adina Traila, Margit Serban, Daniel Coriu
Publikováno v:
Medicina, Vol 59, Iss 10, p 1821 (2023)
Background and Objectives: Despite the vast heterogeneity in the genetic defects causing hemophilia A (HA), large intron inversions represent a major cause of disease, accounting for almost half of the cases of severe HA worldwide. We investigated th
Externí odkaz:
https://doaj.org/article/e54957c7546c486cba33e66922c6dd97
Autor:
Delia Codruţa Popa, Andreea Şerbănică, Radu Obrisca, Ionut Şerbănică, Letiţia Radu, Cristina Jercan, Andra Marcu, Ana Bica, Minodora Asan, Mădălina Petran, Mihaela Dragomir, Cerasela Jardan, Valeria Ţică, Anca Gheorghe, Irina Stoian, Daniel Coriu, Anca Coliţă, Andrei Coliţă
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Acute lymphoblastic leukemia (ALL) is the most frequent childhood cancer, with 80–85% represented by B cell ALL and only 15% by T cell ALL. T Cell ALL (T-ALL) carries a more reserved prognosis compared to B Cell ALL (B-ALL) with regard to response
Externí odkaz:
https://doaj.org/article/20273a428980449b87811819bec5c3b1
Autor:
Andreea Nicoleta Serbanica, Delia Codruta Popa, Constantin Caruntu, Sergiu Pasca, Cristian Scheau, Ionut Vlad Serbanica, Raluca Suciu, Valeria Tica, Elisa Busescu, Luminita Nicoleta Cima, Cerasela Jardan, Mihaela Dragomir, Daniel Coriu, Andrei Colita, Anca Colita
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 4, p 1451 (2023)
B-cell precursor acute lyphoblastic leukemia (ALL) is a common pediatric malignancy and patients may have significant benefits from monoclonal antibodies therapy with increased survival rates. Positive CD20 expression is identified in about half of t
Externí odkaz:
https://doaj.org/article/d1d18fe770a04e87931b625c70bc3f5a
Autor:
Nicoleta Pirciulescu, Mihnea-Alexandru Gaman, Marina Mihailescu, Cristina Constantin, Mihaela Dragomir, Camelia Dobrea, Simona Costache, Iulia Ursuleac, Daniel Coriu, Ana Manuela Crisan
Publikováno v:
Medicina, Vol 58, Iss 12, p 1798 (2022)
Introduction: Essential thrombocythemia is a chronic myeloproliferative neoplasm associated with thrombo-hemorrhagic events and the progression to myelofibrosis or acute myeloid leukemia. The purpose of this article is to present real-world data on E
Externí odkaz:
https://doaj.org/article/114935ce814147a88fc0030889e45319
Autor:
Andreea Jercan, Amalia Ene, Ruxandra Jurcut, Mirela Draghici, Sorina Badelita, Mihaela Dragomir, Camelia Dobrea, Monica Popescu, Dumitru Jardan, Emanuel Stoica, Speranta Iacob, Ionela Codita, Claudiu Stan, Daniel Coriu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background In Romania, 23 patients have been diagnosed with hereditary transthyretin amyloidosis (ATTRh), 18 of whom have the Glu54Gln mutation. This retrospective cohort included all patients with Glu54Gln-mutated ATTRh who were diagnosed i
Externí odkaz:
https://doaj.org/article/c2b271c673c24582aaa937c8667f0036
Autor:
Letitia-Elena Radu, Andrei Colita, Sergiu Pasca, Ciprian Tomuleasa, Codruta Popa, Catalin Serban, Anca Gheorghe, Andreea Serbanica, Cristina Jercan, Andra Marcu, Ana Bica, Patric Teodorescu, Catalin Constantinescu, Bobe Petrushev, Minodora Asan, Cerasela Jardan, Mihaela Dragomir, Alina Tanase, Anca Colita
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
Introduction: Childhood acute lymphoblastic leukemia (ALL) is a hematologic malignancy characterized by the acquisition of several genetic lesions in the lymphoid progenitors with subsequent proliferation advantage and lack of maturation. Along the y
Externí odkaz:
https://doaj.org/article/19bdc832da5d43a380225e67120599af
Autor:
Onda T. Lupu, Bogdan Popescu, Elena Avram, Mihaela Dragomir, Gheorghe Dănuț Cimponeriu, Ioana Mighiu, Silvia Aposteanu, Daniel Coriu
Publikováno v:
Revista Romana de Medicina de Laborator. 30:261-272
Introduction: Acute promyelocytic leukemia (APL) is defined by the PML-RARA fusion gene. APL treatment can have significant side effects, therefore the development of optimal therapeutic options is crucial. Although the study of miRNAs is still in it
Autor:
Alexandra Ghiaur, Bogdan Ionescu, Cristina Constantin, Didona Vasilache, Mihaela Dragomir, Daniel Coriu
Publikováno v:
Clinical Lymphoma Myeloma and Leukemia. 22:S241-S242