Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ghali Benouna"'
Autor:
Ghali Bennani, Soukaina Zahri, Mohamed Khaldi, Ghali Benouna, Abdenasser Drighil, Rachida Habbal
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-5 (2024)
Abstract Background Kallmann–Morsier syndrome is a rare disease characterized by the association of congenital gonadotropic deficiency and anosmia or hyposmia. The cardiac manifestations associated with this syndrome are little known. Through this
Externí odkaz:
https://doaj.org/article/ea72cbaacb19459cad20f5dc9a9f89a1
Publikováno v:
International Journal of Nutrition Sciences, Vol 5, Iss 3, Pp 126-133 (2020)
Background: Hepatic steatosis is widely considered as the hepatic manifestation of metabolic syndrome. The effect of argan oil consumption on the possible hepatic complications of metabolic syndrome has been evaluated in this study. Methods:Twenty-ni
Externí odkaz:
https://doaj.org/article/fda8ad82f5ba420bb605288ec84741a1
Akademický článek
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Autor:
Noël Mahoungou-Mackonia, Maria Khalil, Karim Fatiha, Imad Nouamou, Salim Arous, Ghali Benouna, Abdenasser Drighil, Leila Azzouzi, Rachida Habbal
Publikováno v:
Cardiology and Angiology: An International Journal. 12:28-33
Introduction: Benign intracardiac tumours are the most common of the 5% of primary tumours and account for 90% of intracardiac tumours. Myxoma, which is the main benign tumour, rarely localizes to the mitral valve, in the order of 1-5%, associated wi
Autor:
A. Fadoul Tahir, M. Njie, P. M. Mulendele, M. Foudail, M. Haboub, S. Arous, M. Ghali Benouna, A. Drighil, L. Azzouzi, R. Habbal
Publikováno v:
Cardiology and Angiology: An International Journal. :19-25
LVNC (left ventricular non-compaction) is a rare congenital cardiomyopathy with a reported incidence of 0.05% in adults. It can occur in isolation or affect both ventricles. It’s characterized by prominent LV trabeculae and deep intertrabecular rec
Autor:
R. Habbal, L. Azouzi, A. Drighil, M. Ghali Benouna, S. Arous, M. Haboub, P. M. Mulendele, Boutar M. Sidi, A. Fadoul Tahir, M. Njie
Publikováno v:
Cardiology and Angiology: An International Journal. :430-436
Acute aortic dissection on bicuspid aortic valve (BAV) type 0 is a rare especially in young masculine. Risk factors like smoking and intensive sport activities can hasten their apparition especially in non-diagnosed population. Trans thoracic echocar
Publikováno v:
Journal of Medical Case Reports, Vol 11, Iss 1, Pp 1-5 (2017)
Abstract Background Hemorrhagic complications are quite common in the rare cases where thrombolysis is performed. Ischemic stroke in the aftermath of thrombolysis for a ST elevation myocardial infarction is a very rare and paradoxical complication. W
Externí odkaz:
https://doaj.org/article/6711fcaa91704adcbbc4acb4e0e83ff0
Autor:
Mahamadou Charfo, Asmaa ELAMRAOUI, Sadissou GAMBOBO, Meryem HABOUB, Salim AROUSS, Ghali BENOUNA, Rachida HABBAL
Introduction: Cardiac myxoma is a primary benign tumor most often located in the left atrium and it is a rare source of cerebral stroke of young subjects. Case Presentation: We report the case of a young women with cardiac myxoma revelated by hemiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83f7118d86d7ab5df7269bbfb43f8de6
https://doi.org/10.21203/rs.3.rs-1978256/v1
https://doi.org/10.21203/rs.3.rs-1978256/v1
Autor:
Noël Mahoungou-Mackonia, Meriem Mousaid, Nassour Brahim, Meryem Haboub, Arous Salim, Ghali Benouna, Abdenasser Drighil, Leila Azzouzi, Rachida Habbal
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 72:101600
Autor:
El Ghali Benouna, Leila Azzouzi, Abdenasser Drighil, Serbout Saousan, Adnane Hind, Rachida Habbal
Publikováno v:
Journal of Heart. 1:20-23
Systemic lupus erythematosus is an autoimmune inflammatory disease of unknown etiology, the coronary lesions are extremely rare, and in particular the coronary aneurysms. We report a case of a coronary aneurysm of a patient diagnosed with Systemic lu