Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Neale, Nicola"'
Publikováno v:
In Progress in Pediatric Cardiology December 2022 67
Autor:
Abhinav Agarwal, Suad R Al Amer, Habib Al Tarif, Aieshah Ahmed Ismael, Abdulla Faisal Alshaiji, Vimalarani Arulselvam, Neale Nicola Kalis
Publikováno v:
Heart Views, Vol 23, Iss 2, Pp 78-85 (2022)
Introduction: Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease. Surgical correction has improved survival but re-intervention is often required. Objectives: The objective is to assess outcomes after surgical repair of TO
Externí odkaz:
https://doaj.org/article/a9ca5839ed654550865eec868e1db3a1
Autor:
Abhinav Agarwal, Ramaning Loni, Suad Rashid Al Amer, Vimalarani Arulselvam, Neale Nicola Kalis
Publikováno v:
Indian Pediatrics Case Reports, Vol 1, Iss 2, Pp 120-123 (2021)
Background: Critical congenital heart disease (CCHD) encompasses congenital structural heart defects that cause significant morbidity and mortality in the first few weeks of life unless treated and/or require surgery or catheter intervention within t
Externí odkaz:
https://doaj.org/article/ea3ddc0488a442fa8dbca0df4186dbb7
Publikováno v:
Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging, Vol 5, Iss 3, Pp 207-210 (2021)
Crossed pulmonary artery (CPA) is a rare congenital malformation with only about 100 cases reported worldwide. It is often an incidental finding on cardiac imaging with symptoms rarely attributed to this anomaly. Sometimes, it can result in difficult
Externí odkaz:
https://doaj.org/article/34f1abc2b6404b39a5be5264bccb1073
Autor:
Faisal Waheed Aloqab, Mohamed Ramzi Almajed, Noor Arif Binsanad, Saud Rashid Al Amer, Neale Nicola Kalis
Publikováno v:
Birth Defects Research. 115:764-769
Publikováno v:
Heart Views, Vol 19, Iss 1, Pp 16-19 (2018)
We report a case with recoarctation within a tubed graft. Covered stent placed inside the tube graft safely and effectively treated the recoarctation of the aorta.
Externí odkaz:
https://doaj.org/article/6912324a25ec4a0d8c353152ba80570d
Publikováno v:
Heart Views, Vol 18, Iss 1, Pp 21-25 (2017)
Williams–Beuren syndrome is a multisystem genetic disorder caused by hemizygous deletion on chromosome 7q11.23, encompassing about 28 genes including the elastin gene, ELN. Cardiovascular abnormalities are frequent and are related to elastin insuff
Externí odkaz:
https://doaj.org/article/dbf9de6e0dd744a3b3c18a48a5c9c9a0
Akademický článek
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Publikováno v:
Journal of the Bahrain Medical Society. 34:40-43
Depression in pregnancy is being recognized as a major contributor to adverse maternal and fetal outcomes. Recent years have seen significant research focused on the development of safe pharmacological methods to treat depression in pregnancy, result