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Gabriel-Petre Gorecki

Biographic Data

ID8260651
NAMEGabriel-Petre Gorecki
GIVEN NAMESGabriel-Petre
FAMILY NAMEGorecki
SIGNATUREGORECKI G
AFFILIATIONSClinical Emergency Hospital Bucharest
ORCID0000-0002-5340-8929
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2024
LATEST PUBLICATION YEAR2026
H-INDEX0
  • Preventable Infectious Pathology Dominates Neonatal Readmissions

    Open Access•Daniela-Eugenia Popescu, Ioana Roșca et al.•ARTICLE•Children•2026

    Background: Readmission of newborns within the first 28 days after initial discharge represents a significant healthcare concern, causing distress to families and financial burden on healthcare systems. Understanding readmission patterns and risk factors is essential for implementing preventive strategies. Objective: This retrospective observational study aimed to evaluate the prevalence and characteristics of neonatal readmissions to a pediatric…

  • Prenatal Features of Mirage Syndrome—Case Report and Review of the Literature

    Open Access•Anca Maria Panaitescu, Iulia Huluță et al.•ARTICLE•Children•2024

    MIRAGE syndrome is a recently described congenital condition characterized genetically by heterozygous gain-of-function missense mutations in the growth repressor sterile alpha domain containing 9 (SAMD9) located on the arm of chromosome 7 (7q21.2). The syndrome is rare and is usually diagnosed in newborns and children with myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy, hence the acronym…

No prominent works on this page.

  • Prenatal Features of Mirage Syndrome—Case Report and Review of the Literature

    Open Access•Anca Maria Panaitescu, Iulia Huluță et al.•ARTICLE•Children•2024

    MIRAGE syndrome is a recently described congenital condition characterized genetically by heterozygous gain-of-function missense mutations in the growth repressor sterile alpha domain containing 9 (SAMD9) located on the arm of chromosome 7 (7q21.2). The syndrome is rare and is usually diagnosed in newborns and children with myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy, hence the acronym…

  • Preventable Infectious Pathology Dominates Neonatal Readmissions

    Open Access•Daniela-Eugenia Popescu, Ioana Roșca et al.•ARTICLE•Children•2026

    Background: Readmission of newborns within the first 28 days after initial discharge represents a significant healthcare concern, causing distress to families and financial burden on healthcare systems. Understanding readmission patterns and risk factors is essential for implementing preventive strategies. Objective: This retrospective observational study aimed to evaluate the prevalence and characteristics of neonatal readmissions to a pediatric…

Amniocentesis (1 work) · Biology (1 work) · Breastfeeding (1 work) · Bronchiolitis (1 work) · Congenital gastrointestinal and neural anomalies (1 work) · Epidemiology (1 work) · Esophageal and GI Pathology (1 work) · Exome sequencing (1 work) · Fetus (1 work) · Genetic counseling (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