Ștefana Maria Moisă

ORCID: 0000-0003-4140-0492
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About
Contact & Profiles
Research Areas
  • Palliative Care and End-of-Life Issues
  • Congenital Heart Disease Studies
  • Romani and Gypsy Studies
  • Cardiac Arrhythmias and Treatments
  • Cardiac electrophysiology and arrhythmias
  • Gastroesophageal reflux and treatments
  • Lipoproteins and Cardiovascular Health
  • Childhood Cancer Survivors' Quality of Life
  • Congenital Diaphragmatic Hernia Studies
  • Vascular Malformations and Hemangiomas
  • Mechanical Circulatory Support Devices
  • Hematological disorders and diagnostics
  • Patient Dignity and Privacy
  • Atrial Fibrillation Management and Outcomes
  • Cardiovascular Effects of Exercise
  • Genetics and Neurodevelopmental Disorders
  • Medical Malpractice and Liability Issues
  • Cardiac tumors and thrombi
  • Interpreting and Communication in Healthcare
  • Infectious Diseases and Tuberculosis
  • Hyperglycemia and glycemic control in critically ill and hospitalized patients
  • Ethics in medical practice
  • Venous Thromboembolism Diagnosis and Management
  • Cystic Fibrosis Research Advances
  • Eosinophilic Esophagitis

Grigore T. Popa University of Medicine and Pharmacy
2013-2025

Clinical Emergency Hospital Bucharest
2022-2024

Weatherford College
2021

Iuliu Hațieganu University of Medicine and Pharmacy
2019

Spitalul Clinic de Urgență pentru Copii Cluj-Napoca
2011-2014

Spitalul Clinic de Recuperare
2009-2013

Hai phong University Of Medicine and Pharmacy
2012

Wolf–Parkinson–White (WPW) syndrome is a disorder characterized by the presence of at least one accessory pathway (AP) that can predispose people to atrial/ventricular tachyarrhythmias and even sudden cardiac death. It second most common cause paroxysmal supraventricular tachycardia in parts world, affecting about 0.1–0.3% general population. Most patients with WPW have normal anatomy, but it may be associated concomitant congenital heart disease or systemic diseases. Although many...

10.3390/diagnostics14030296 article EN cc-by Diagnostics 2024-01-30

Background: Nowadays it is considered that a specific causal relationship exists between asthma and gastroesophageal reflux (GER), because of the aspiration gastric refluate which leads to maintain spasticity even real crisis paroxystic expiratory dyspnea. This study explores this evaluates results after treatment. Methods: 56 children diagnosed with asthma, hospitalized in regional center pediatric gastroenterology Northeast Romania, underwent 24-hour continuous esophageal pH monitoring...

10.3390/children9030336 article EN cc-by Children 2022-03-02

Congenital hyperinsulinism (CHI) is a rare disorder of glucose metabolism and the most common cause severe persistent hypoglycemia (hyperinsulinemic hypoglycemia, HH) in neonatal period childhood. Most cases are caused by mutations ABCC8 KCNJ11 genes that encode ATP-sensitive potassium channel (KATP). We present correlation between genetic heterogeneity variable phenotype patients with early-onset HH gene mutations. In first patient, who presented since day life, molecular testing revealed...

10.3390/ijms25105533 article EN International Journal of Molecular Sciences 2024-05-19

Background: Biomarkers, electrocardiogram (ECG) and Holter ECG are basic, accessible feasible cardiac investigations. The combination of their results may lead to a more complex predictive model that improve the clinical approach in acute heart failure (AHF). main objective was investigate which parameters correlated with usual biomarkers (prohormone N-terminal proBNP, high-sensitive troponin I) patients failure, population from Romania. relationship between certain support future research...

10.3390/diagnostics12123037 article EN cc-by Diagnostics 2022-12-03

Maturity-onset diabetes of the young (MODY) is part heterogeneous group monogenic (MD) characterized by non-immune dysfunction pancreatic β-cells. The diagnosis MODY still remains a challenge for clinicians, with many cases being misdiagnosed as type 1 or 2 mellitus (T1DM/T2DM), and over 80% remaining undiagnosed. With introduction modern technologies, important progress has been made in deciphering molecular mechanisms etiology MD, including MODY. aim our study was to identify genetic...

10.3390/ijms25126318 article EN International Journal of Molecular Sciences 2024-06-07

Gastroschisis is a congenital abdominal wall defect that presents an increasing occurrence at great cost for the health system. The aim of study to detect main factors unfavorable evolution in case gastroschisis and find best predictors death.we conducted retrospective cohort neonates with treated tertiary pediatric center during last 30 years; 159 patients were eligible study. Logistic regression was used determine risk death, estimated based on independent variables previously validated by...

10.3390/jpm11111168 article EN Journal of Personalized Medicine 2021-11-09
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