Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ali Alakhfash"'
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:
Journal of the Saudi Heart Association, Vol 27, Iss 4, p 324 (2015)
This is a rare congenital heart disease case of unguarded mitral valve orifice, transposition of great vessels, and pulmonary atresia with a dilated left ventricle that has not been reported. Case presentation: A 3 kg, Saudi, female neonate presented
Externí odkaz:
https://doaj.org/article/4ac801ffb10344618da842f3604ff38a
Autor:
Areej Alotaibi, Ghadir A Alakhfash, Ali Alakhfash, Tayseer Mahmoud, Alhasan A Alakhfash, Abdullah Al Qwaee, Abdulrahman Mesned
Publikováno v:
Cureus. 14(6)
Objectives This study aims to evaluate the value of Holter monitoring in pediatric cases and look for the best predictor for abnormal Holter monitoring. Methodology All patients referred with cardiac symptoms associated or possibly related to abnorma
Autor:
Khaled Alhawri, Ali Alakhfash, Abdullah Alqwaee, Mohammed HassabElnabi, Fazel Ahmed, Mohammed Alhawri, Bana Nasser, Marwan Alhoobani, Giusseppe Mazzesi, Abdulraoof Alsaeedi, Abdulrahman Almesned
Publikováno v:
Journal of Cardiac Surgery. 36
Autor:
Ali A. Al-Akhfash, Ghadeer Ali Alakhfash, Abdullah Alqwaiee, Athkar Alhajjaj, Abdulrahman Almesned
Publikováno v:
Respiratory Medicine Case Reports, Vol 31, Iss, Pp 101286-(2020)
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports
Pulmonary arterial hypertension associated with congenital heart disease (PAH-CHD) is one type under group 1 PH. Undiagnosed or delayed diagnosis of significant CHD might lead to significant PAH and at the end might lead to Eisenmenger syndrome. We c
Autor:
Zarghuna M A, Shinwari, Abdulrahman, Almesned, Ali, Alakhfash, Ahmad M, Al-Rashdan, Eissa, Faqeih, Zainab, Al-Humaidi, Ahmed, Alomrani, Malak, Alghamdi, Dilek, Colak, Abdullah, Alwadai, Monther, Rababh, Majid, Al-Fayyadh, Zuhair N, Al-Hassnan
Publikováno v:
Cardiology. 137(3)
Cardiomyopathy (CMP) in children is a clinically and genetically heterogeneous group of disorders. Disease-associated mutations have been identified in more than 50 genes. Recently, mutations in the mitochondrial tRNA processing gene, ELAC2, were rep