Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Setalia, Popa"'
Autor:
Lăcrămioara Ionela Butnariu, Delia Andreia Bizim, Carmen Oltean, Cristina Rusu, Monica Cristina Pânzaru, Gabriela Păduraru, Nicoleta Gimiga, Gabriela Ghiga, Ștefana Maria Moisă, Elena Țarcă, Iuliana Magdalena Starcea, Setalia Popa, Laura Mihaela Trandafir
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 12, p 6318 (2024)
Maturity-onset diabetes of the young (MODY) is part of the heterogeneous group of monogenic diabetes (MD) characterized by the non-immune dysfunction of pancreatic β-cells. The diagnosis of MODY still remains a challenge for clinicians, with many ca
Externí odkaz:
https://doaj.org/article/be52cdcd516f4b7ba989b7109e2473c9
Autor:
Lăcrămioara Ionela Butnariu, Delia Andreia Bizim, Gabriela Păduraru, Luminița Păduraru, Ștefana Maria Moisă, Setalia Popa, Nicoleta Gimiga, Gabriela Ghiga, Minerva Codruța Bădescu, Ancuta Lupu, Ioana Vasiliu, Laura Mihaela Trandafir
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 10, p 5533 (2024)
Congenital hyperinsulinism (CHI) is a rare disorder of glucose metabolism and is the most common cause of severe and persistent hypoglycemia (hyperinsulinemic hypoglycemia, HH) in the neonatal period and childhood. Most cases are caused by mutations
Externí odkaz:
https://doaj.org/article/06d4eaa7767842e2af2516de1efd88c2
Autor:
Monica-Cristina Pânzaru, Setalia Popa, Ancuta Lupu, Cristina Gavrilovici, Vasile Valeriu Lupu, Eusebiu Vlad Gorduza
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
The corpus callosum is the largest white matter structure connecting the two cerebral hemispheres. Agenesis of the corpus callosum (ACC), complete or partial, is one of the most common cerebral malformations in humans with a reported incidence rangin
Externí odkaz:
https://doaj.org/article/2ce992ed2f1f432fb10d12e6be44bfbe
Autor:
Lăcramioara Ionela Butnariu, Eusebiu Vlad Gorduza, Elena Țarcă, Monica-Cristina Pânzaru, Setalia Popa, Simona Stoleriu, Vasile Valeriu Lupu, Ancuta Lupu, Elena Cojocaru, Laura Mihaela Trandafir, Ștefana Maria Moisă, Andreea Florea, Laura Stătescu, Minerva Codruța Bădescu
Publikováno v:
Diagnostics, Vol 13, Iss 14, p 2348 (2023)
Atherogenic dyslipidemia plays a critical role in the development of metabolic syndrome (MetS), being one of its major components, along with central obesity, insulin resistance, and hypertension. In recent years, the development of molecular genetic
Externí odkaz:
https://doaj.org/article/ad39512519eb42e49cb6ba48b811cb05
Autor:
Daniela Luminita Zob, Iolanda Augustin, Lavinia Caba, Monica-Cristina Panzaru, Setalia Popa, Alina Delia Popa, Laura Florea, Eusebiu Vlad Gorduza
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 1, p 716 (2022)
Melanoma is a common and aggressive tumor originating from melanocytes. The increasing incidence of cutaneous melanoma in recent last decades highlights the need for predictive biomarkers studies. Melanoma development is a complex process, involving
Externí odkaz:
https://doaj.org/article/a639d78e1eca4699b9f93dee269f0a45
Autor:
Lăcrămioara Ionela Butnariu, Eusebiu Vlad Gorduza, Laura Florea, Elena Țarcă, Ștefana Maria Moisă, Laura Mihaela Trandafir, Simona Stoleriu, Minerva Codruța Bădescu, Alina-Costina Luca, Setalia Popa, Iulian Radu, Elena Cojocaru
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12199 (2022)
Vascular anomalies (VAs) are morphogenesis defects of the vascular system (arteries, capillaries, veins, lymphatic vessels) singularly or in complex combinations, sometimes with a severe impact on the quality of life. The progress made in recent year
Externí odkaz:
https://doaj.org/article/c61ec932963f492e86a0b7fc984efecb
Autor:
Roxana Popescu, Mihaela Grămescu, Lavinia Caba, Monica-Cristina Pânzaru, Lăcrămioara Butnariu, Elena Braha, Setalia Popa, Cristina Rusu, Georgeta Cardos, Monica Zeleniuc, Violeta Martiniuc, Cristina Gug, Luminiţa Păduraru, Maria Stamatin, Carmen C. Diaconu, Eusebiu Vlad Gorduza
Publikováno v:
Genes, Vol 12, Iss 1957, p 1957 (2021)
Genes
Genes
We present a complex chromosomal anomaly identified using cytogenetic and molecular methods. The child was diagnosed during the neonatal period with a multiple congenital anomalies syndrome characterized by: flattened occipital region; slight turrice
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42a9e67d95bacf6e8c60619b2b2a4201
https://www.mdpi.com/2073-4425/12/12/1957
https://www.mdpi.com/2073-4425/12/12/1957
Autor:
Setalia, Popa1 setalia_ostapov@yahoo.com, Viviana, Aursulesei2,3, Genoveva, Baroi3,4, Anca, Ivanov3,5, Ingrith, Miron3,5, Datcu, D. M.2,3
Publikováno v:
Acta Medica Marisiensis. 2012, Vol. 58 Issue 5, p347-349. 3p. 1 Black and White Photograph.
Autor:
Butnariu, Lăcrămioara Ionela1 (AUTHOR) ionela.butnariu@umfiasi.ro, Russu, Georgiana2 (AUTHOR) g_russu@yahoo.com, Luca, Alina-Costina2,3 (AUTHOR) alina.luca@umfiasi.ro, Sandu, Constantin4 (AUTHOR) sandu.v.constantin@umfiasi.ro, Trandafir, Laura Mihaela3 (AUTHOR) gabriela.ghiga@umfiasi.ro, Vasiliu, Ioana5 (AUTHOR) ioana.vasiliu@umfiasi.ro, Popa, Setalia1 (AUTHOR) ionela.butnariu@umfiasi.ro, Ghiga, Gabriela3 (AUTHOR), Bălănescu, Laura6 (AUTHOR) laura7balanescu@yahoo.com, Țarcă, Elena7 (AUTHOR) tarca.elena@umfiasi.ro
Publikováno v:
International Journal of Molecular Sciences. Oct2024, Vol. 25 Issue 20, p11173. 26p.
Publikováno v:
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi. 117(1)
Peripheral artery disease (PAD) is a common condition. Over the past 20 years the risk factors for PAD have changed.To identify the regional characteristics of the patients with PAD and the sex- and urban/rural-related differences.Retrospective study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::743a598cb84306eb8a4376de664e2cde
https://pubmed.ncbi.nlm.nih.gov/24505899
https://pubmed.ncbi.nlm.nih.gov/24505899