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
Autor:
Ali A. Alakhfash, Abdullah Alqwaiee, Ghadeer Ali Alakhfash, Athkar Alhajjaj, Abdulrahman A. Almesned
Publikováno v:
Respiratory Medicine Case Reports, Vol 31, Iss , Pp 101286- (2020)
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
Externí odkaz:
https://doaj.org/article/3c337a6bc1fb4ddb93b728233f5548aa
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e897400e299df05240e33f5356081e3
https://pubmed.ncbi.nlm.nih.gov/35812585
https://pubmed.ncbi.nlm.nih.gov/35812585
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::834cd616b12fe48fb3c5781b17c98bbc
https://doi.org/10.1111/jocs.15825
https://doi.org/10.1111/jocs.15825
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e243414922c254c0467988743da3a772
https://pubmed.ncbi.nlm.nih.gov/28441660
https://pubmed.ncbi.nlm.nih.gov/28441660