Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Motea E. Elhoury"'
Autor:
Abdalrahman A. Alhassan, Ayed A. Shati, Sami M. Al-Ahmari, Afia E. Elhadam, Tajudeen M. Bushari, Omer H. Elhag, Motea E. Elhoury
Publikováno v:
Cardiology in the Young. 32:1196-1201
Malposition of the branch pulmonary arteries (MBPA) is an unusual malformation characterised by anomalous origin of both pulmonary arteries from the main pulmonary trunk. To date, only few cases have been reported. Herein, we present the first case r
Publikováno v:
Saudi Medical Journal
Saudi Medical Journal, Vol 38, Iss 7, Pp 764-767 (2017)
Saudi Medical Journal, Vol 38, Iss 7, Pp 764-767 (2017)
Scimitar syndrome is a variant of partial anomalous pulmonary venous connection (PAPVC), in which all or part of the right lung is drained by right pulmonary veins that anomalously connect to the inferior vena cava (IVC). The affected lung and its as
Publikováno v:
Cardiology in the Young. 25:81-86
Geleophysic dysplasia is an extremely rare acromelic skeletal dysplasia resembling lysosomal storage disease. It is characterised by characteristic facial phenotype, short stature, micromelia, joint contracture, and early cardiac valvular involvement
Publikováno v:
Congenital Heart Disease. 5:620-623
Percutaneous closure of secundum atrial septal defect (ASD II) is considered the treatment of choice in the majority of cases. Interrupted inferior vena cava with azygos continuation can make delivery of the occluder difficult or not possible. Transj
Autor:
Milad El-Segaier, Mohammed Omar Galal, Abdulrahman Almoukirish, Abdalla Saeed, Motea E. Elhoury
Publikováno v:
Pediatric cardiology. 37(3)
Infants with post-tricuspid valve shunts (PTS) may benefit from interatrial communication (IAC). The effect of IAC on left ventricular (LV) performance in these patients was studied. IAC was documented prospectively in 55 patients with PTS. Clinical
Combination of right and left ventricular outflow tracts obstruction is extremely rare. Neonates with combined aortic stenosis (AS) and pulmonary stenosis (PS) present in critical condition and required urgent treatment. The management approach is no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1494654ae2e9f12d082bb537012dddc
Publikováno v:
Journal of the Saudi Heart Association. 25:151
Background Geleophysic dysplasia is an extremely rare autosomal recessive acromelic skeletal dysplasia characterized by short stature and short limbs, joint contracture and cardiac involvement. It has been described worldwide in less than 40 patients
Autor:
Alhassan, Abdalrahman A., Shati, Ayed A., Al-Ahmari, Sami M., Elhadam, Afia E., Bushari, Tajudeen M., Elhag, Omer H., Elhoury, Motea E.
Publikováno v:
Cardiology in the Young; Aug2022, Vol. 32 Issue 8, p1196-1201, 6p
Publikováno v:
Saudi Medical Journal; Jul2017, Vol. 38 Issue 7, p764-767, 4p
Publikováno v:
Pediatric Cardiology; Mar2016, Vol. 37 Issue 3, p582-592, 11p, 4 Charts, 1 Graph