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Setalia Popa

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Articles by Setalia Popa

Vitamin C: From Self-Sufficiency to Dietary Dependence in the Framework of Its Biological Functions and Medical Implications

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By Setalia Popa, Andrei Mihai Cristian
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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IJMS | Free Full-Text | Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability

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By Delia Andreia Bizim, Setalia Popa, Nicoleta Gimiga, Gabriela Ghiga
| MDPI
All articles published by MDPI are made immediately available worldwide under an open access license. No special permission is required to reuse all or part of the article published by MDPI, including figures and tables. For articles published under an open access Creative Common CC BY license, any part of the article may be reused without permission provided that the original article is clearly cited. For more information, please refer to https://www.mdpi.com/openaccess.
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Genetic Heterogeneity Correlated with Phenotypic Variability in Congenital Hyperinsulinism Caused by Mutation in ABCC8 Gene Associated with Early‐Onset Persistent Neonatal Hypoglycemia

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By Setalia Popa, Nicoleta Gimiga, Delia Andreia Bizim, Gabriela Ghiga
| Preprints.org
Preprint Article Version 1 This version is not peer-reviewed Version 1 : Received: 28 March 2024 / Approved: 29 March 2024 / Online: 29 March 2024 (08:08:35 CET) Butnariu, L.I.; Bizim, D.A.; Păduraru, G.; Păduraru, L.; Moisă, Ș.M.; Popa, S.; Gimiga, N.; Ghiga, G.; Bădescu, M.C.; Lupu, A.; Vasiliu, I.; Trandafir, L.M. Genetic Heterogeneity Correlated with Phenotypic Variability in Congenital Hyperinsulinism Caused by Mutation in ABCC8 Gene Associated with Early‐Onset Persistent Neonatal...
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Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome

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By Eusebiu Vlad Gorduza, Monica-Cristina Panzaru, Simona Stoleriu, Setalia Popa
| MDPI
Abstract : 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 genetics techniques and extended analysis at the genome or exome level has led to important progress in the identification of genetic factors (heritability) involved in lipid metabolism disorders associated with MetS.
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