Antoneta Dacia Petroaie
Biographic Data
| ID | 8258899 |
|---|---|
| NAME | Antoneta Dacia Petroaie |
| GIVEN NAMES | Antoneta Dacia |
| FAMILY NAME | Petroaie |
| SIGNATURE | PETROAIE A D |
| AFFILIATIONS | Grigore T. Popa University of Medicine and Pharmacy |
| ORCID | 0000-0002-1239-8058 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2020 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
PEX6 Mutation in a Child with Infantile Refsum Disease—A Case Report and Literature Review
The aim of this paper is to describe the temporal progression and clinical picture of a 2-year-old child with infantile Refsum disease, as well as the diagnostic procedures performed; this case presented multiple hematologic, metabolic, and developmental complications and progressive disabilities. Genetic testing revealed a mutation of the PEX6 (Peroxisomal Biogenesis Factor 6) gene, and the metabolic profile was consistent with the diagnosis. Pa…
A Call to Action
Living in a digital era when most women can enjoy the benefits of easy access to a wealth of online information does not guarantee that mothers-to-bear aware of healthy dietary and nutrition recommendations for pregnancy and the lactation period. Our study aimed to survey the awareness of pregnant women from urban and rural North Eastern Romania in order to identify potential knowledge gaps or misconceptions and suggest solutions to achieve adequ…
No prominent works on this page.
A Call to Action
Living in a digital era when most women can enjoy the benefits of easy access to a wealth of online information does not guarantee that mothers-to-bear aware of healthy dietary and nutrition recommendations for pregnancy and the lactation period. Our study aimed to survey the awareness of pregnant women from urban and rural North Eastern Romania in order to identify potential knowledge gaps or misconceptions and suggest solutions to achieve adequ…
PEX6 Mutation in a Child with Infantile Refsum Disease—A Case Report and Literature Review
The aim of this paper is to describe the temporal progression and clinical picture of a 2-year-old child with infantile Refsum disease, as well as the diagnostic procedures performed; this case presented multiple hematologic, metabolic, and developmental complications and progressive disabilities. Genetic testing revealed a mutation of the PEX6 (Peroxisomal Biogenesis Factor 6) gene, and the metabolic profile was consistent with the diagnosis. Pa…
Biology (2 works) · Medicine (2 works) · Advertising (1 work) · Bioinformatics (1 work) · Breastfeeding Practices and Influences (1 work) · Business (1 work) · Call to action (1 work) · Disease (1 work) · Endocrine system (1 work) · Environmental health (1 work)