Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Rachida, Amri"'
Publikováno v:
Annales de cardiologie et d'angeiologie.
Absent pulmonary valve syndrome is a rare congenital heart disease. Associated with ventricular septal defect, it is considered a rare variant of Tetralogy of Fallot "Tetralogy of Fallot with absent pulmonary valve syndrome". It is characterized by i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4f5cc1ce3805b3cdf32f5c5b288c2f0f
https://pubmed.ncbi.nlm.nih.gov/36535847
https://pubmed.ncbi.nlm.nih.gov/36535847
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 72:101573
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1cb9c4006d6aa710e9224e2316b4c9cc
https://doi.org/10.1016/j.ancard.2022.11.008
https://doi.org/10.1016/j.ancard.2022.11.008
Autor:
Raid Faraj, Abakar Bachar, Oussama Sidaty, Asmaa Bouamoud, Zineb Fassi Fehri, Fatima-zahrae Chrifi, Fatima Chikhi, Ibtissam Fellat, Rachida Amri, Mohamed Cherti
Publikováno v:
Annals of Medicine & Surgery. 76
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd08b50189647fe3fd708d8ce87ad69e
https://doi.org/10.1016/j.amsu.2022.103500
https://doi.org/10.1016/j.amsu.2022.103500
Autor:
Raid Faraj, Ahmed Djibril, Fatima-Azzahra Benmessaoud, Mohamed Benasser, Jamila Zarzur, Latifa Oukerraj, Rachida Amri, Mohamed Cherti
Publikováno v:
Annals of Medicine & Surgery. 75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08f50cd9a75895d4b408838a482b44da
https://doi.org/10.1016/j.amsu.2022.103465
https://doi.org/10.1016/j.amsu.2022.103465
Publikováno v:
World journal for pediatriccongenital heart surgery. 11(4)
Anomalous left coronary artery from the pulmonary artery (ALCAPA) was described by Abbott in 1908. In most cases, it is an isolated lesion, being the most common cause of myocardial ischemia in children. The associated mortality rate without interven
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0d70244db22c389a45c71d5e4ed50e
https://pubmed.ncbi.nlm.nih.gov/30336750
https://pubmed.ncbi.nlm.nih.gov/30336750
Publikováno v:
Journal of the Saudi Heart Association. 25:99-101
The simple transposition of the great arteries is a lethal congenital heart disease. The life expectancy of unoperated patients is about 9months.We report the original observation of a girl with unoperated simple transposition of the great arteries,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871950bc421b471a12723ec61289de4e
https://doi.org/10.1016/j.jsha.2012.10.001
https://doi.org/10.1016/j.jsha.2012.10.001
Publikováno v:
La Presse Médicale. 41:328-330
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f83545d787f6ef5f3e27c3e26f980674
https://doi.org/10.1016/j.lpm.2011.05.023
https://doi.org/10.1016/j.lpm.2011.05.023
Autor:
Yasser Otmani, Younes Cheikhaoui, Hind Khiari, Reda Ajaja, Fadoua Lachhab, Mina Amellal, Younes Chajai, Rachida Amri, Younes Alaoui, Ibtissam Fikri, Laila Haddour
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 2:520-522
A rare case of a newborn with situs inversus totalis associated with simple transposition of the great arteries is reported. A successful anatomical surgical repair was accomplished on day 10 of life, consisting of an arterial switch operation with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::276f9d01f41ac56ce0e595adea849f7b
https://doi.org/10.1177/2150135111405346
https://doi.org/10.1177/2150135111405346
Publikováno v:
Cardiology in the Young. 20:562-564
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e25bd0f63f86c8d3895fea471c12507
https://doi.org/10.1017/s1047951110000855
https://doi.org/10.1017/s1047951110000855
Publikováno v:
Cardiology in the young. 24(2)
Behçet's disease is a chronic autoimmune disease with vascular complications that are most frequently manifested as thromboembolism in veins and pseudoaneurysm in arteries. We report the case of a 13-year-old boy admitted for clinical and biological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa5ac9b7da32347e1d9fa4534184c39b
https://pubmed.ncbi.nlm.nih.gov/23659210
https://pubmed.ncbi.nlm.nih.gov/23659210