Giovanni Meliota
Biographic Data
| ID | 8260999 |
|---|---|
| NAME | Giovanni Meliota |
| GIVEN NAMES | Giovanni |
| FAMILY NAME | Meliota |
| SIGNATURE | MELIOTA G |
| AFFILIATIONS | Pediatric Cardiology Unit, Giovanni XXIII Pediatric Hospital, 70126 Bari, Italy |
| ORCID | 0000-0002-9924-4915 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
Anomalous Coronary Artery Origin from Pulmonary Artery and Coronary Fistulas
Anomalous coronary artery origin from pulmonary artery and coronary-pulmonary fistulas are the major causes of ischemic cardiopathy in children. Both anomalies are characterized by a connection between a higher and a lower pressure chamber causing coronary steal. However, several mechanisms and associated lesions may be responsible of the different presentations of the "coronary steal phenomenon". The aim of this review is to highlight the differ…
Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome
Loeys-Dietz syndrome (LDS) is a rare autosomal-dominant disorder of the connective tissue with some typical vascular findings, skeletal manifestations, craniofacial features, and cutaneous findings with a wide phenotypic spectrum. Six different genes are involved in LDS and the diagnosis is based on the identification of a heterozygous pathogenic variant in TGFBR1 , TGFBR2 , SMAD3 , TGFB2 , TGFB3 , or SMAD2 in children with suggestive findings. T…
No prominent works on this page.
Cleft Palate and Aortic Dilatation as Clues for Loeys–Dietz Syndrome
Loeys-Dietz syndrome (LDS) is a rare autosomal-dominant disorder of the connective tissue with some typical vascular findings, skeletal manifestations, craniofacial features, and cutaneous findings with a wide phenotypic spectrum. Six different genes are involved in LDS and the diagnosis is based on the identification of a heterozygous pathogenic variant in TGFBR1 , TGFBR2 , SMAD3 , TGFB2 , TGFB3 , or SMAD2 in children with suggestive findings. T…
Anomalous Coronary Artery Origin from Pulmonary Artery and Coronary Fistulas
Anomalous coronary artery origin from pulmonary artery and coronary-pulmonary fistulas are the major causes of ischemic cardiopathy in children. Both anomalies are characterized by a connection between a higher and a lower pressure chamber causing coronary steal. However, several mechanisms and associated lesions may be responsible of the different presentations of the "coronary steal phenomenon". The aim of this review is to highlight the differ…
Artery (1 work) · Bone and Dental Protein Studies (1 work) · Cardiovascular Issues in Pregnancy (1 work) · Congenital Heart Disease Studies (1 work) · Connective tissue (1 work) · Connective Tissue Disorder (1 work) · Connective tissue disorders research (1 work) · Coronary arteries (1 work) · Coronary Artery Anomalies (1 work) · Coronary artery anomaly (1 work)