Showing results (71-80 of 89) with videos related to
Sort By:
Pageof 9
Journal of Dermatological Science|December 6, 2018
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axisHadla Hariri, Mazen Kurban, Christiane Al-Haddad, et al.Journal of Cardiovascular Electrophysiology|November 8, 2024
Cardiac Ablation in the Pediatric Population at a Tertiary Care Center in a Developing CountryZiad Bulbul, Alaaeddine El Ghazawi, Alicia Khazzeka, et al.Cardiology in the Young|March 13, 2025
Chylothorax: a rare postoperative complication in paediatric cardiac surgery patients - a 15-year retrospective study from a tertiary care centre in a developing countryBshara Sleem, Jad Abdul Khalek, Adham Makarem, et al.Molecular Genetics & Genomic Medicine|April 12, 2016
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patientKameel Kassab, Hadla Hariri, Lara Gharibeh, et al.Pediatric Cardiology|January 5, 2019
Transcatheter Closure of Atrial Septal Defects: Comparable Experience and Outcomes Between Developing and Developed CountriesAhmad Almanla, Fatme Charafeddine, Mohamad Abutaqa, et al.Pediatric Cardiology|March 19, 2021
Congenital Heart Disease in Syrian Refugee Children: The Experience at a Tertiary Care Center in a Developing CountryHala Mostafa, Moustafa Rashed, Majdulddine Azzo, et al.International Journal of Cardiology|December 24, 2017
Percutaneous pulmonary valve implantation in small conduits: A multicenter experienceSebastien Hascoet, José Diogo Martins, Haysam Baho, et al.Pediatric Cardiology|January 19, 2024
Establishing a High-Quality Pediatric Cardiac Surgery Program in Post-Conflict Regions: A Model for Limited Resource CountriesTammam Youssef, Fouad Bitar, Hassanain Alogla, et al.Perfusion|March 15, 2019
Establishing an ECMO program in a developing country: challenges and lessons learnedJana Assy, Hadi Skouri, Lama Charafeddine, et al.European Journal of Dermatology : EJD|July 26, 2017
Mutations in the ABCG8 gene are associated with sitosterolaemia in the homozygous form and xanthelasmas in the heterozygous formTara Bardawil, Abdallah Rebeiz, Myriam Chaabouni, et al.Pageof 9