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Darina Krumova

Biographic Data

ID8264256
NAMEDarina Krumova
GIVEN NAMESDarina
FAMILY NAMEKrumova
SIGNATUREKRUMOVA D
AFFILIATIONSMedical University of Varna
VERIFIEDNo
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2025
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Possibilities and Limitations of Prenatal Diagnosis of Rare Imprinting Syndromes

    Open Access•Simona Anzhel, Nikolinka Yordanova et al.•ARTICLE•Children•2026

    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

    Open Access•Adriana Hadzhieva-Hristova, Darina Krumova et al.•ARTICLE•Children•2025

    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

    Open Access•Adriana Hadzhieva-Hristova, Darina Krumova et al.•ARTICLE•Children•2025

    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

    Open Access•Simona Anzhel, Nikolinka Yordanova et al.•ARTICLE•Children•2026

    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)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae