Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Valeriu Moldovan"'
Autor:
Adela Nechifor-Boilă, Ancuţa Zahan, Claudia Bănescu, Valeriu Moldovan, Doina Piciu, Septimiu Voidăzan, Angela Borda
Publikováno v:
Cancers, Vol 15, Iss 16, p 4053 (2023)
We aimed to evaluate the prognostic value of BRAFV600E mutation in a series of 127 papillary thyroid carcinoma (PTC) cases as a single factor, and in synergic interaction with other standard risk factors. BRAFV600E mutation was assessed by real-time
Externí odkaz:
https://doaj.org/article/ba84c93dda9445b3a81b2f2c45b91a2a
Autor:
Anca Delia Mare, Cristina Nicoleta Ciurea, Adrian Man, Bianca Tudor, Valeriu Moldovan, Luminița Decean, Felicia Toma
Publikováno v:
Gastroenterology Insights, Vol 12, Iss 1, Pp 28-40 (2021)
Diarrheal disease is still a major public health concern, as it is still considered an important cause of death in children under five years of age. A few decades ago, the detection of enteropathogenic E. coli was made by detecting the O, H, and K an
Externí odkaz:
https://doaj.org/article/b02ac92aef81428e8c89b1a47efa183e
Autor:
Simona Loredana Vasilache, Anastasia Boaghi, Raluca-Monica Pop, Claudia Bănescu, Valeriu Moldovan, Carmen Duicu, Ionela Maria Paşcanu, Oana Mărginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 69, Iss 4, Pp 300-304 (2020)
Obiective. Numeroși factori au fost asociați cu creșterea prevalenţei obezităţii, alimentaţia fiind cel mai important factor. Scopul acestui studiu a fost evaluarea comportamentului alimentar la copiii şcolari din Târgu Mureş şi evaluarea
Externí odkaz:
https://doaj.org/article/5c63d14fabd04053b82f58d4763fd8fc
Autor:
Simona Loredana Vasilache, Anastasia Boaghi, Raluca-Monica Pop, Claudia Banescu, Valeriu Moldovan, Carmen Duicu, Ionela Maria Pascanu, Oana Marginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 69, Iss 4, Pp 295-299 (2020)
Objectives. Numerous factors have been associated with hight prevalence of obesity, nutrition being the most important factor. The aim of this study was to evaluate the eating behavior of school children in Targu Mures and to evaluate the impact on a
Externí odkaz:
https://doaj.org/article/8c6a4f3c1b3b4269bafc00dd0a8f4409
Autor:
Anca Meda Georgescu, Claudia Banescu, Razvan Azamfirei, Adina Hutanu, Valeriu Moldovan, Iudita Badea, Septimiu Voidazan, Minodora Dobreanu, Ioana Raluca Chirtes, Leonard Azamfirei
Publikováno v:
BMC Infectious Diseases, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract Background The goal of the study was to evaluate a potential role for tumor necrosis factor alpha (TNF-α) genetic variability as biomarker in sepsis. In particular, we aimed to determine if single nucleotide polymorphisms (SNPs) of TNF-α g
Externí odkaz:
https://doaj.org/article/9bd75e4a023147339dbbe4df45299ded
Publikováno v:
Anatolian Journal of Cardiology, Vol 23, Iss 3, Pp 120-127 (2020)
Familial hypercholesterolemia (FH) is considered the genetic cause of coronary heart disease and ischemic stroke. FH is mainly an autosomal codominant pattern-based disorder and is primarily determined by point mutations within the low-density lipopr
Externí odkaz:
https://doaj.org/article/b0eb563aff8b493496cc01ef4029f4c4
Autor:
Alina Scridon, Vasile Bogdan Halaţiu, Alkora Ioana Balan, Dan Alexandru Cozac, Valeriu Moldovan, Claudia Bănescu, Marcel Perian, Răzvan Constantin Şerban
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Background: The complex interactions that exist between the pacemaker current, If, and the parasympathetic nervous system could significantly influence the course of patients undergoing chronic therapy with the If blocker ivabradine. We thus aimed to
Externí odkaz:
https://doaj.org/article/27d8a690476b456c98f5ab09d3bc3929
Autor:
Simona Loredana Vasilache, Adelina Micheu, Claudia Banescu, Valeriu Moldovan, Carmen Duicu, Ionela Maria Pascanu, Oana Marginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 66, Iss 4, Pp 248-251 (2017)
Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused by lack of expression of genes on the paternally inherited chromosome 15q11.2-q13 region. There are three major genetic subtypes in PWS: paternal 15q11-q13 deletion (70%
Externí odkaz:
https://doaj.org/article/7a32bc3bfce04116beca4b5573f57fd8
Autor:
Simona Loredana Vasilache, Adelina Micheu, Claudia Bănescu, Valeriu Moldovan, Carmen Duicu, Ionela Maria Paşcanu, Oana Mărginean
Publikováno v:
Romanian Journal of Pediatrics, Vol 66, Iss 4, Pp 283-286 (2017)
Sindromul Prader-Willi (SPW) reprezintă o afecţiune genetică complexă, multisistemică, cauzată de lipsa expresiei genelor din regiunea q11.2-q13 a cromozomului 15 patern. Există trei subtipuri genetice majore în SPW: deleţia paternă din re
Externí odkaz:
https://doaj.org/article/d1aadb8ffaee43b29dede8ad6547e2e6
Autor:
Anca Negovan, Mihaela Iancu, Valeriu Moldovan, Septimiu Voidazan, Simona Bataga, Monica Pantea, Kinga Sarkany, Cristina Tatar, Simona Mocan, Claudia Banescu
Publikováno v:
Gastroenterology Research and Practice, Vol 2016 (2016)
Background. Aspirin use for cardiovascular or cancer prevention is limited due to its gastrointestinal side effects. Objective. Our prospective, observational case-control study aims to identify the predictive factors for ulcers in low-dose aspirin c
Externí odkaz:
https://doaj.org/article/f9aa036cbec24445b207480c86164e59