Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andrei Pîrvu"'
Autor:
Bianca Petre-Mandache, Emilia Burada, Mihai Gabriel Cucu, Diter Atasie, Anca-Lelia Riza, Ioana Streață, Radu Mitruț, Răzvan Pleșea, Amelia Dobrescu, Andrei Pîrvu, Gabriela Popescu-Hobeanu, Paul Mitruț, Florin Burada
Publikováno v:
Current Oncology, Vol 31, Iss 10, Pp 6406-6418 (2024)
Colorectal cancer (CRC) is a major public health problem worldwide, currently ranking third in cancer incidence and second in mortality. Multiple genes and environmental factors have been involved in the complex and multifactorial process of CRC carc
Externí odkaz:
https://doaj.org/article/f47b0aa1510d4090890fd2665d485e79
Autor:
Elena Anca Pinoșanu, Denisa Pîrșcoveanu, Carmen Valeria Albu, Emilia Burada, Andrei Pîrvu, Roxana Surugiu, Raluca Elena Sandu, Alina Florina Serb
Publikováno v:
Current Issues in Molecular Biology, Vol 46, Iss 4, Pp 3484-3501 (2024)
Ischemic stroke triggers a complex cascade of cellular and molecular events leading to neuronal damage and tissue injury. This review explores the potential therapeutic avenues targeting cellular signaling pathways implicated in stroke pathophysiolog
Externí odkaz:
https://doaj.org/article/7d9e3e11eaa246c4bd3627f246715de6
Autor:
Ioana Streață, Alexandru Caramizaru, Anca-Lelia Riza, Simona Șerban-Sosoi, Andrei Pîrvu, Monica-Laura Cara, Mihai-Gabriel Cucu, Amelia Mihaela Dobrescu, Ro-NMCA-ID Group, CExBR Pediatric Neurology Obregia Group, CExBR Pediatric Neurology “V. Gomoiu” Hospital Group, Elena-Silvia Shelby, Adriana Albeanu, Florin Burada, Mihai Ioana
Publikováno v:
Diagnostics, Vol 12, Iss 12, p 3137 (2022)
The investigation of unexplained global developmental delay (GDD)/intellectual disability (ID) is challenging. In low resource settings, patients may not follow a standardized diagnostic process that makes use of the benefits of advanced technologies
Externí odkaz:
https://doaj.org/article/09c88a287b2a4ef8af2ea46572d5411f
Autor:
Rodica Diaconu, Andreea-Ramona Dumitrașcu, Elisa Liehn, Andrei Pîrvu, Mihai Ioana, Dragoș Alexandru, Eugen Țieranu, Tudor-Adrian Bălșeanu, Ionuț Donoiu
Publikováno v:
Romanian Journal of Cardiology. 33:19-24
Background: Apolipoprotein E (ApoE) is a ubiquitous protein involved in maintaining cholesterol homeostasis and lipoprotein clearance from circulation. It is coded by three alleles (ε2, ε3, ε4) with six genotypes (ε3/ε3, ε3/ε4, ε2/ε3, ε4/ε
Autor:
Anca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș, Andrei Pîrvu, Diana Miclea, Gheorghe Mihuț, Răzvan-Mihail Pleșea, Delia Ștefan, Mihaela Drodar, Călin Lazăr, null on behalf of the HINT Study, null on behalf of the FUSE Study, Mihai Ioana, Radu Popp
Publikováno v:
Genes; Volume 14; Issue 1; Pages: 69
The genetic causes of autosomal recessive nonsyndromic hearing loss (ARNSHL) are heterogeneous and highly ethnic-specific. We describe GJB2 (connexin 26) variants and carrier frequencies as part of our study and summarize previously reported ones for
Autor:
Elena-Silvia Shelby, Michael Morris, Liliana Pădure, Andrada Mirea, Relu Cocoș, Alexandru Cărămizaru, Simona Șerban-Sosoi, Andrei Pîrvu, Ioana Streață
Publikováno v:
Genes; Volume 13; Issue 2; Pages: 212
19q13 microdeletion syndrome is a very rare genetic disease characterized by pre- and postnatal growth retardation, intellectual disability, expressive language impairment, ectodermal dysplasia, and slender habitus. Since the description of the first
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