Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Valerica BELENGEANU"'
Autor:
Daniela-Eugenia Popescu, Simona Cerbu, Ioana Rosca, Nicoleta Lungu, Ana Adriana Trușculescu, Valerica Belengeanu, Aniko Maria Manea, Mirabela Adina Dima, Florin Gorun, Zoran Laurentiu Popa, Doru Ciprian Crisan, Marioara Boia
Publikováno v:
Children, Vol 10, Iss 8, p 1370 (2023)
The aim of this study is to evaluate the test results of neonates delivered by COVID-19-positive mothers during pregnancy with those of neonates born to unvaccinated mothers who are COVID-19-free. A cohort study was conducted on 367 pregnant women wh
Externí odkaz:
https://doaj.org/article/23d100b86dee4e858ee4e4d42a4af1f4
Autor:
Daniela-Eugenia Popescu, Cosmin Cîtu, Ana Maria Cristina Jura, Nicoleta Lungu, Dan Navolan, Marius Craina, Alin Semenescu, Florin Gorun, Mihai-Andrei Jura, Valerica Belengeanu, Marioara Boia
Publikováno v:
Vaccines, Vol 10, Iss 6, p 848 (2022)
When the first vaccines against SARS-CoV-2 emerged, pregnant women were excluded from clinical trials, so vaccine recommendations were initially adjourned, with late initiation for this populational category. The present study aims to quantify the se
Externí odkaz:
https://doaj.org/article/5421f860f321428c8f26fd81cf020e48
Autor:
Valerica, Belengeanu, Diana, Marian, Tiberiu, Hosszu, Alexandru Simion, Ogodescu, Alina Draga, Belengeanu, Christian, Samoilă, Paul, Freiman, Ioana Elena, Lile
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 60(2)
Orofaciodigital syndrome (OFDS) is a collective term for a rare inherited disorder that displays a wide phenotypic and genetic heterogeneity. The findings of diagnostic are the combination of the characteristic oral, facial and digital anomalies. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2e4a9a7f83a043d373833ad9a44cf6ca
https://pubmed.ncbi.nlm.nih.gov/31658347
https://pubmed.ncbi.nlm.nih.gov/31658347
Autor:
Ioan Ioiart, Valerica Belengeanu, Imola Miklos, Dragos V. Nica, Alin Grelus, Cristina Popescu
Publikováno v:
International Journal of Molecular Sciences, Vol 18, Iss 11, p 2465 (2017)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
This is the first study investigating the clinical relevance of 5-hydroxymethylcytosine (5hmC) in genomic DNA from white blood cells (WBC) in the context of prostate cancer (PCa) and other prostate pathologies. Using an enzyme-linked immunosorbent as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b21f3a5fee158e11aad36bfa6736ebb
https://www.mdpi.com/1422-0067/18/11/2465
https://www.mdpi.com/1422-0067/18/11/2465
Autor:
Nicoleta ANDREESCU, Dorina STOICANESCU, Alina BELENGEANU, Simona FARCAS, Cristina POPA, Monica STOIAN, Valerica BELENGEANU
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVII, Iss 1, Pp 9-13 (2010)
Breast cancer is among the most common forms of cancer. The molecular mechanisms involved in hormone dependence of breast cancer have been largely investigated. The role of the estrogen and progesterone receptors has been documented, but the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::26235fbde288f8e6f603fa9e20692d5c
Publikováno v:
Analele Universitatii din Oradea: Fascicula Biologie, Vol TOM XVI, Iss 2, Pp 138-141 (2009)
Rare disorders are defined as diseases, including those of genetic origin, which are life-threatening or chronically debilitating, which are of such low prevalence that special combined efforts are needed to address them. We present a case with a rar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::810d3ebac7df3e29e04c594d8fe9b330
Autor:
Valerica Belengeanu
Publikováno v:
Acta Endocrinologica (Bucharest). 4:87-97
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45889bdf7c784bee786aafbd39aeb0e3
https://doi.org/10.4183/aeb.2008.87
https://doi.org/10.4183/aeb.2008.87
Autor:
Valerica Belengeanu, Eirik Frengen, Nicoleta Andreescu, Alina Belengeanu, Thilini H. Gamage, Doriana Misceo, Simona Farcas, Monica Stoian
Publikováno v:
Gene. 539(1)
We report a 20-month-old girl ascertained at the age of 11 months for developmental delay. She presented with hypotonia and delayed motor development. The patient had severe language impairment and showed behaviour consistent with autism spectrum dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bdf0cb9281f9311273fd7ec53e180f7
https://pubmed.ncbi.nlm.nih.gov/24508274
https://pubmed.ncbi.nlm.nih.gov/24508274
Autor:
Luminita Pilat, David Chirila, Calin Popa, Doriana Misceo, Valerica Belengeanu, Ilinca Frunza, Cristina Popescu, Monica Stoian, Viorica Leordean, Alina Belengeanu
Publikováno v:
Current Opinion in Biotechnology. 24:S97-S98
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f099dbcc1071f9a8f190895ce22b63d3
https://doi.org/10.1016/j.copbio.2013.05.293
https://doi.org/10.1016/j.copbio.2013.05.293
Autor:
Valerica, Belengeanu, Kinga, Rozsnyai, Cristina, Gug, Mariana, Bănăţeanu, Simona, Farcaş, Alina, Belengeanu
Publikováno v:
Clinical dysmorphology. 13(4)
We report two siblings with congenital generalized hypertrichosis and distinctive facial appearance consistent with the dysmorphic facial features described in Ambras syndrome. The patients were born to non-consanguineous, phenotypically normal paren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7eda881443faf86be90a69bc1b9417d1
https://pubmed.ncbi.nlm.nih.gov/15365467
https://pubmed.ncbi.nlm.nih.gov/15365467