Zobrazeno 1 - 10
of 172
pro vyhledávání: '"Chaikhouni, A."'
Autor:
Karaolanis, Georgios I., Makaloski, Vladimir, Jungi, Silvan, Weiss, Salome, Kotopoulos, Konstantinos, Chaikhouni, Basel, Becker, Daniel, Kotelis, Drosos, Bosiers, Michel J.
Publikováno v:
In Journal of Vascular Surgery August 2024
Autor:
Manal Alaamery, Nour Albesher, Fahad Alhabshan, Phil Barnett, Mohamed Salim Kabbani, Farah Chaikhouni, Aho Ilgun, Olaf R. F. Mook, Hessa Alsaif, Vincent M. Christoffels, Peter van Tintelen, Arthur A. M. Wilde, Arjan C. Houweling, Salam Massadeh, Alex V. Postma
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 10, Iss 11, p 455 (2023)
Background: Congenital heart diseases (CHD) are the most common congenital malformations in newborns and remain the leading cause of mortality among infants under one year old. Molecular diagnosis is crucial to evaluate the recurrence risk and to add
Externí odkaz:
https://doaj.org/article/9f1524d26e144b9f88b2e4419e250bd4
Autor:
Amer Chaikhouni
Publikováno v:
Heart Views, Vol 21, Iss 3, Pp 235-237 (2020)
Externí odkaz:
https://doaj.org/article/0e3865ae9011485f95c30aa3275352e5
Akademický článek
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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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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K zobrazení výsledku je třeba se přihlásit.
Autor:
Alaamery, Manal, Albesher, Nour, Alhabshan, Fahad, Barnett, Phil, Salim Kabbani, Mohamed, Chaikhouni, Farah, Ilgun, Aho, Mook, Olaf R. F., Alsaif, Hessa, Christoffels, Vincent M., van Tintelen, Peter, Wilde, Arthur A. M., Houweling, Arjan C., Massadeh, Salam, Postma, Alex V.
Publikováno v:
Journal of Cardiovascular Development & Disease (JCDD); Nov2023, Vol. 10 Issue 11, p455, 14p
Publikováno v:
International Journal of Pediatrics and Adolescent Medicine, Vol 8, Iss 3, Pp 198-202 (2021)
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics & Adolescent Medicine
Background and Objective Despite improvement in medical management, infective endocarditis (IE) remains a serious disease that may affect children with and without preexisting cardiac conditions with significant morbidity and mortality. Neurological
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d3c1d3877671e1bdedef6c3949364b
https://doi.org/10.1016/j.ijpam.2021.02.003
https://doi.org/10.1016/j.ijpam.2021.02.003
Autor:
Suliman Khan, Aida M. Bertoli-Avella, Atia Sheereen, Iman Almohammed, Ingrid M.E. Frohn-Mulder, Peter Bauer, Salam Massadeh, Ingrid M.B.H. van de Laar, Farah Chaikhouni, Amal Alhashem, Manal Alaamery, Fahad Alhabshan, Mohamed S. Kabbani, Bader Alghamdi, Natalia Ordonez, Salem Alawbathani, Marja W. Wessels, Christian Beetz, Salim Ahmad
Publikováno v:
BASE-Bielefeld Academic Search Engine
Clinical Genetics, 98(1), 56-63. Wiley-Blackwell Publishing Ltd
Clinical Genetics, 98(1), 56-63. Wiley-Blackwell Publishing Ltd
Recently, ADAMTS19 was identified as a novel causative gene for autosomal recessive heart valve disease (HVD), affecting mainly the aortic and pulmonary valves. Exome sequencing and data repository (CentoMD) analyses were performed to identify patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dce6ca1456f5efb87c22843403defd0
https://pure.eur.nl/en/publications/1c7efecf-6b63-49e1-97f0-e55faecb4914
https://pure.eur.nl/en/publications/1c7efecf-6b63-49e1-97f0-e55faecb4914
Autor:
Salam Massadeh, Fahad Alhabshan, Hadeel N. AlSudairi, Sarah Alkwai, Moneera Alsuwailm, Mohamed S. Kabbani, Farah Chaikhouni, Manal Alaamery
Publikováno v:
Genes; Volume 13; Issue 2; Pages: 236
Frank–Ter Haar syndrome (FTHS), sometimes referred to as Ter Haar syndrome, is a rare hereditary disorder that manifests in skeletal, cardiac, and ocular anomalies, including hypertelorism, glaucoma, prominent eyes, and facial abnormalities. In thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30f7e1b16e4ea6bac9fa67aac95cfdfa