Zobrazeno 1 - 10
of 458
pro vyhledávání: '"S, Kabbani"'
Autor:
Bana Agha Nasser, Mesned Abdulrahman, Abdullah A. L. Qwaee, Ali Alakhfash, Tageldein Mohamad, Mohamed S. Kabbani, Usama Alseedi, Baraa Obedien, Abdulaziz Chrit
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 70, Iss 1, Pp 1-8 (2022)
Abstract Objective To assess the effect of cardiac surgery on growth catch-up of Down syndrome (DS) children with failure to thrive (FTT) and congenital heart disease (CHD) and investigate other causes of FTT in DS children. Method We conducted a ret
Externí odkaz:
https://doaj.org/article/b405d3808f874321bca3923d72a12eb0
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0291766 (2023)
Tissue engineering has driven significant research in the strive to create a supply of tissues for patient treatment. Cell integration into engineered tissues maximizes functional capabilities, however, issues of rejection remain. Autologous cell sou
Externí odkaz:
https://doaj.org/article/f98bd23e1897430c9f5bf50d94e34adc
Publikováno v:
Egyptian Pediatric Association Gazette, Vol 69, Iss 1, Pp 1-8 (2021)
Abstract Background Children with congenital heart disease (CHD) frequently become malnourished due to many factors including hypermetabolic state, inadequate caloric intake, malabsorption, and fluid restriction as part of the hemodynamic interventio
Externí odkaz:
https://doaj.org/article/6141bc93b367496ea5ea5dc842c6a518
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-16 (2021)
Abstract The ideal engineered vascular graft would utilize human-derived materials to minimize foreign body response and tissue rejection. Current biological engineered blood vessels (BEBVs) inherently lack the structure required for implantation. We
Externí odkaz:
https://doaj.org/article/f58c798d1ddb41d187fde00eb1e8f423
Publikováno v:
Case Reports in Vascular Medicine, Vol 2022 (2022)
Raynaud’s phenomenon of the tongue after radiation therapy with or without chemotherapy is an exceedingly rare complication. Symptoms are similar to Raynaud’s disease of other sites and involve pallor and discomfort on exposure to cold temperatur
Externí odkaz:
https://doaj.org/article/d3aca907d41b4c53a6daffc0c785a3d6
Publikováno v:
Journal of the Saudi Heart Association, Vol 31, Iss 4, Pp 161-169 (2019)
Background and aim: Children who suffer cardiopulmonary arrest (CPA) after cardiac surgery frequently survive with return of spontaneous circulation. However, their neurodevelopmental outcomes and performance are still unclear. The aim of this study
Externí odkaz:
https://doaj.org/article/93280a28c9de423f9de2597f5c410ce0
Autor:
Bana Agha Nasser, Abdullah Al Qwaee, Abdul Rahman Almesned, Ali Akhfash, Tagelden Mohamad, Farah Chaikhouni, Fahad Alhabshan, Mohamed S. Kabbani
Publikováno v:
Journal of the Saudi Heart Association, Vol 31, Iss 2, Pp 51-56 (2019)
Although infective endocarditis is an uncommon condition, it can be fatal if not treated. The new era of infective endocarditis in children with structurally normal heart has become apparent entity. Duke criteria has been established for a long time
Externí odkaz:
https://doaj.org/article/7d23937ff5d9480da29c4ac4e0221155
Effects of protocol-based management on the post-operative outcome after systemic to pulmonary shunt
Autor:
Sameh R. Ismail, Muneira M. Almazmi, Rajab Khokhar, Wedad AlMadani, Ali Hadadi, Omar Hijazi, Mohamed S. Kabbani, Ghassan Shaath, Mahmoud Elbarbary
Publikováno v:
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 271-278 (2018)
Objectives: Systemic to pulmonary shunt (commonly known as Modified Blalock–Taussig shunt) is a palliative procedure in cyanotic heart diseases to overcome inadequate blood flow to the lungs. Based on the most recent risk stratification score, the
Externí odkaz:
https://doaj.org/article/aeaafcc391c94f379136b0cd09782995
Publikováno v:
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 455-459 (2018)
Late onset of complete heart block is a life-threatening uncommon complication after surgical repair of congenital heart diseases. In this report, we discuss two cases of Perimembranous ventricular septal defect (VSD) that had late presentation of co
Externí odkaz:
https://doaj.org/article/99e1c203a8cd42e3a4ea47a50c7e173f
Autor:
Maria L. Bello Valls, Hiba G. Salih, Osama M. El Dadah, Abdullah A. Alghamdi, Fahad Alhabshan, Sameh R. Ismail, Talat M. Yelbuz, Mohamed S. Kabbani
Publikováno v:
The Egyptian Heart Journal, Vol 70, Iss 4, Pp 255-260 (2018)
Objectives: Coarctation of the aorta represents 5–8% of all congenital heart diseases. Children with severe coarctation of the aorta may present with significant depression of myocardial function. The aim of this study is to identify short and midt
Externí odkaz:
https://doaj.org/article/8dc64fa254a041c0ba1bf98ab467ff1b