Darina Krumova
Biographic Data
| ID | 8264256 |
|---|---|
| NAME | Darina Krumova |
| GIVEN NAMES | Darina |
| FAMILY NAME | Krumova |
| SIGNATURE | KRUMOVA D |
| AFFILIATIONS | Medical University of Varna |
| VERIFIED | No |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes
Background: Prader-Willi syndrome (PWS) is a multisystemic complex imprinting disorder. Prenatal diagnosis of PWS is still a challenge with non-specific ultrasound markers and limitations for diagnosis with non-invasive screening methods. Prenatal suspicion and early postnatal diagnosis are essential for promoting healthy growth and development, preventing complications, and providing healthcare professionals and families with the necessary suppo…
Assessment of Phoenix Sepsis Score, pSofa, Pelod-2, and PRISM III in Pediatric Intensive Care
Background/Objectives : Early identification of pediatric sepsis complications in intensive care is challenging and requires improved diagnostic tools. This study aimed to compare the Phoenix Sepsis Score (PSS), pSOFA, PELOD-2, and PRISM III in assessing clinical complexity in children with septic and critical conditions in the PICU and to identify the most suitable scale for this patient cohort. Methods : Data were collected prospectively from 5…
No prominent works on this page.
Assessment of Phoenix Sepsis Score, pSofa, Pelod-2, and PRISM III in Pediatric Intensive Care
Background/Objectives : Early identification of pediatric sepsis complications in intensive care is challenging and requires improved diagnostic tools. This study aimed to compare the Phoenix Sepsis Score (PSS), pSOFA, PELOD-2, and PRISM III in assessing clinical complexity in children with septic and critical conditions in the PICU and to identify the most suitable scale for this patient cohort. Methods : Data were collected prospectively from 5…
Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes
Background: Prader-Willi syndrome (PWS) is a multisystemic complex imprinting disorder. Prenatal diagnosis of PWS is still a challenge with non-specific ultrasound markers and limitations for diagnosis with non-invasive screening methods. Prenatal suspicion and early postnatal diagnosis are essential for promoting healthy growth and development, preventing complications, and providing healthcare professionals and families with the necessary suppo…
Assisted Reproductive Technology and Twin Pregnancy (1 work) · Cohort (1 work) · Disaster Response and Management (1 work) · Emergency Medicine (1 work) · Fetus (1 work) · Genetic counseling (1 work) · Genetic diagnosis (1 work) · Genetic Syndromes and Imprinting (1 work) · Genetic testing (1 work) · Imprinting (psychology (1 work)