Found: 25
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Nosocomial Infections Affecting Newborns with Abdominal Wall Defects.
- Published in:
- Healthcare (2227-9032), 2023, v. 11, n. 8, p. 1131, doi. 10.3390/healthcare11081131
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- Article
Statistical Analysis of the Main Risk Factors of an Unfavorable Evolution in Gastroschisis.
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- Journal of Personalized Medicine, 2021, v. 11, n. 11, p. 1168, doi. 10.3390/jpm11111168
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- Article
Differential diagnosis difficulties related to infantile hemangioma -- case report and literature review.
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- Romanian Journal of Morphology & Embryology, 2019, v. 60, n. 4, p. 1375
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- Publication type:
- Article
The Genetic Architecture of Vascular Anomalies: Current Data and Future Therapeutic Perspectives Correlated with Molecular Mechanisms.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12199, doi. 10.3390/ijms232012199
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- Article
Modern Treatment of Valvulopathies in Patients with Congenital Hemophilia.
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- Life (2075-1729), 2024, v. 14, n. 3, p. 354, doi. 10.3390/life14030354
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- Publication type:
- Article
Acute Myocardial Infarction in Patients with Hereditary Thrombophilia—A Focus on Factor V Leiden and Prothrombin G20210A.
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- Life (2075-1729), 2023, v. 13, n. 6, p. 1371, doi. 10.3390/life13061371
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- Publication type:
- Article
An Up-to-Date Literature Review on Ventricular Assist Devices Experience in Pediatric Hearts.
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- Life (2075-1729), 2022, v. 12, n. 12, p. 2001, doi. 10.3390/life12122001
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- Publication type:
- Article
Myocardial Ischemia Related to Common Cancer Therapy—Prevention Insights.
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- Life (2075-1729), 2022, v. 12, n. 7, p. 1034, doi. 10.3390/life12071034
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- Publication type:
- Article
Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?
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- Life (2075-1729), 2022, v. 12, n. 6, p. 865, doi. 10.3390/life12060865
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- Article
CLEIDOCRANIAL DYSPLASIA: A CASE REPORT.
- Published in:
- 2017
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- Publication type:
- Case Study
Current Challenges in the Treatment of the Omphalocele—Experience of a Tertiary Center from Romania.
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- Journal of Clinical Medicine, 2022, v. 11, n. 19, p. 5711, doi. 10.3390/jcm11195711
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- Publication type:
- Article
Genetic Modifying Factors of Cystic Fibrosis Phenotype: A Challenge for Modern Medicine.
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- Journal of Clinical Medicine, 2021, v. 10, n. 24, p. 5821, doi. 10.3390/jcm10245821
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- Publication type:
- Article
The Role of Natural Extracts in the Management of Infantile Hemangiomas and Vascular Tumors.
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- Pediatric Health, Medicine & Therapeutics, 2024, v. 15, p. 1, doi. 10.2147/PHMT.S439537
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- Publication type:
- Article
Medical Cultural Competence. A Phenomenological Analysis.
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- Romanian Journal for Multidimensional Education / Revista Românească pentru Educaţie Multidimensională, 2024, v. 16, n. 2, p. 447, doi. 10.18662/rrem/16.2/866
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- Publication type:
- Article
Diagnosis and Management of Simple and Complicated Meconium Ileus in Cystic Fibrosis, a Systematic Review.
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- Diagnostics (2075-4418), 2024, v. 14, n. 11, p. 1179, doi. 10.3390/diagnostics14111179
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- Publication type:
- Article
Omphalocele and Cardiac Abnormalities—The Importance of the Association.
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- Diagnostics (2075-4418), 2023, v. 13, n. 8, p. 1413, doi. 10.3390/diagnostics13081413
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- Publication type:
- Article
Ganglioneuroma of the Bladder in Association with Neurofibromatosis Type 1.
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- Diagnostics (2075-4418), 2022, v. 12, n. 12, p. 3126, doi. 10.3390/diagnostics12123126
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- Publication type:
- Article
Cardiovascular Risk Factors in Patients with Congenital Hemophilia: A Focus on Hypertension.
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- Diagnostics (2075-4418), 2022, v. 12, n. 12, p. 2937, doi. 10.3390/diagnostics12122937
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- Publication type:
- Article
An Up-to-Date Narrative Review on Congenital Heart Disease Percutaneous Treatment in Children Using Contemporary Devices.
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- Diagnostics (2075-4418), 2022, v. 12, n. 5, p. N.PAG, doi. 10.3390/diagnostics12051189
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- Publication type:
- Article
Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation.
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- Genes, 2022, v. 13, n. 11, p. 2083, doi. 10.3390/genes13112083
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- Publication type:
- Article
Identification of Genetic Variants Associated with Hereditary Thoracic Aortic Diseases (HTADs) Using Next Generation Sequencing (NGS) Technology and Genotype–Phenotype Correlations.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 20, p. 11173, doi. 10.3390/ijms252011173
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- Publication type:
- Article
The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 12, p. 6318, doi. 10.3390/ijms25126318
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- Publication type:
- Article
Congenital Hyperinsulinism Caused by Mutations in ABCC8 Gene Associated with Early-Onset Neonatal Hypoglycemia: Genetic Heterogeneity Correlated with Phenotypic Variability.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 10, p. 5533, doi. 10.3390/ijms25105533
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- Publication type:
- Article
Advancing Cancer Research: Current Knowledge on Cutaneous Neoplasia.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 13, p. 11176, doi. 10.3390/ijms241311176
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- Publication type:
- Article
Can Bioactive Food Substances Contribute to Cystic Fibrosis-Related Cardiovascular Disease Prevention?
- Published in:
- Nutrients, 2023, v. 15, n. 2, p. 314, doi. 10.3390/nu15020314
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- Publication type:
- Article