Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Farah Chaikhouni"'
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:
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
Autor:
Salam Massadeh, Fahad Alhabshan, Hadeel N. AlSudairi, Sarah Alkwai, Moneera Alsuwailm, Mohamed S. Kabbani, Farah Chaikhouni, Manal Alaamery
Publikováno v:
Genes, Vol 13, Iss 2, p 236 (2022)
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://doaj.org/article/396cfd4ab9094285b480848ed1f4c39b
Autor:
Salam Massadeh, Maha Albeladi, Nour Albesher, Fahad Alhabshan, Kapil Dev Kampe, Farah Chaikhouni, Mohamed S. Kabbani, Christian Beetz, Manal Alaamery
Publikováno v:
Genes, Vol 12, Iss 5, p 612 (2021)
Congenital heart defects (CHDs) are the most common types of birth defects, and global incidence of CHDs is on the rise. Despite the prevalence of CHDs, the genetic determinants of the defects are still in the process of being identified. Herein, we
Externí odkaz:
https://doaj.org/article/6aeaa6cabd9b4c3a86479567cbec8548
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
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
Autor:
Christian Beetz, Salam Massadeh, Mohamed S. Kabbani, Nour Albesher, Kapil Kampe, Farah Chaikhouni, Manal Alaamery, Maha Albeladi, Fahad Alhabshan
Publikováno v:
Genes; Volume 12; Issue 5; Pages: 612
Genes, Vol 12, Iss 612, p 612 (2021)
Genes, Vol 12, Iss 612, p 612 (2021)
Congenital heart defects (CHDs) are the most common types of birth defects, and global incidence of CHDs is on the rise. Despite the prevalence of CHDs, the genetic determinants of the defects are still in the process of being identified. Herein, we
Autor:
Mohamed S. Kabbani, Abdulrahman Almesned, Tagelden Mohamad, Farah Chaikhouni, Ali A. Al Akhfash, Abdullah A.L. Qwaee, Fahad Alhabshan, Bana Agha Nasser
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad1d79524a687e9ad4f76ea75a95c268
https://europepmc.org/articles/PMC6313807/
https://europepmc.org/articles/PMC6313807/