Zobrazeno 1 - 10
of 88
pro vyhledávání: '"Dorra Abid"'
Autor:
Ikhlas Ben Ayed, Amal Bouzid, Fatma Kammoun, Amal souissi, Olfa Jallouli, Salma Mallouli, Souhir Guidara, Salma Loukil, Hajer Aloulou, Fida Jbeli, Sahar Aouichaoui, Dorra Abid, Fatma Abdelhedi, Chahnez Triki, Hassen Kamoun, Saber Masmoudi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background 8q21.11 microdeletion syndrome is a rare chromosomal disorder characterized by recurrent dysmorphic features, a variable degree of intellectual disability and ocular, cardiac and hand/feet abnormalities. To date, ZFHX4 is the only
Externí odkaz:
https://doaj.org/article/a21fb15130e34021bb3464c79a22b09f
Autor:
Salma Charfeddine, Dorra Abid, Rania Hammami, Rania Gargouri, Leila Abid, Faten Triki, Samir Kammoun
Publikováno v:
The Pan African Medical Journal, Vol 38, Iss 29 (2021)
INTRODUCTION: Reduced exercise capacity, coronary artery abnormalities and reversible myocardial ischemia have been demonstrated after arterial switch operation (ASO) and coronary reimplantation. Despite this, indices of systolic function, assessed b
Externí odkaz:
https://doaj.org/article/b00c302d5cc340829379597ce668206b
Autor:
Salma Charfeddine, Dorra Abid, Faten Triki, Souad Mallek, Leila Abid, Samir Kammoun, Ayman Dammak, Imed Frikha
Publikováno v:
Journal of the Saudi Heart Association, Vol 28, Iss 4, Pp 261-265 (2016)
We reported a rare case of non-penetrating chest trauma-induced fistula from the right sinus of Valsalva to the right heart chambers. The ruptured sinus of Valsalva aneurysm was diagnosed preoperatively and operated on successfully. The rarity of thi
Externí odkaz:
https://doaj.org/article/3b01b2b2ee00461e8d280122915f9693
Publikováno v:
The Pan African Medical Journal, Vol 27, Iss 271 (2017)
Sinus of Valsalva aneurysms are extremely rare, and usually of a congenital nature. There are few documented cases of this condition during pregnancy, which renders unclear the therapeutic options. We here report the case of a26 years old pregnant wo
Externí odkaz:
https://doaj.org/article/8ea1d438b6cb426fa8f3b23afde90e4e
Autor:
Rania Hammami, Mouna Boudabbous, Jihen Jdidi, Fatma Trabelsi, Fakher Mroua, Rahma Kallel, Ali Amouri, Dorra Abid, Nabil Tahri, Leila Abid, Samir Kammoun
Publikováno v:
Libyan Journal of Medicine, Vol 12, Iss 1 (2017)
Cirrhotic cardiomyopathy is associated with poor prognosis and risk of acute heart failure after liver transplantation or interventional procedures. We aimed to assess the relationship between the severity of cardiac impairment and hepatic disease. E
Externí odkaz:
https://doaj.org/article/3e52d7379d4146f4993a59013110eec0
Autor:
Salma Charfeddine, Souad Mallek, Faten Triki, Rania Hammami, Dorra Abid, Leila Abid, Samir Kammoun
Publikováno v:
The Pan African Medical Journal, Vol 25, Iss 171 (2016)
INTRODUCTION: the objectives were to assess the left ventricular (LV) structure and function in regularly trained young athletes, using 2 D conventional echocardiographic (echo) methods and speckle tracking echocardiography (STE). An observational cr
Externí odkaz:
https://doaj.org/article/66c3fa6519be4ac99a5f83621c8aa298
Autor:
Rania Hammami, Dorra Abid, Leila Abid, Abir Znazen, Mourad Hentati, Adnene Hammami, Samir Kammoun
Publikováno v:
The Pan African Medical Journal, Vol 16, Iss 24 (2013)
L'endocardite à Bartonalla est une infection ubiquitaire, son diagnostic est difficile vu qu'il s'agit souvent d'endocardite à hémoculture négative. Le but de cette étude est d'analyser les particularités lésionnelles et évolutives de cette e
Externí odkaz:
https://doaj.org/article/742e3c14b4914ee183d44fc2258c7bfc
Publikováno v:
Case Reports in Medicine, Vol 2012 (2012)
Hypertrophic cardiomyopathy (HCM) with midventricular obstruction (MVO) is a rare condition occurring in 1% of HCM patients. It is characterized by asymmetric left ventricular hypertrophy with MVO and elevated intraventricular pressure gradients. Pul
Externí odkaz:
https://doaj.org/article/b57dfcf0512c4542a156ec1e75a31d3e
Publikováno v:
Pan African Medical Journal; Vol. 41 No. 1 (2022)
Le rétrécissement aortique sous-valvulaire reste difficile à prendre en charge, du fait du caractère évolutif imprévisible de la sténose et du taux de récidive élevé après le traitement chirurgical. Les objectifs de notre travail étaient
Autor:
Chahnez Triki, Fatma Kammoun, Saber Masmoudi, Amal Bouzid, Sahar Aouichaoui, Hajer Aloulou, Souhir Guidara, Salma Loukil, Dorra Abid, Salma Zouari Mallouli, Ikhlas Ben Ayed, Olfa Jallouli, Hassen Kamoun, Fida Jbeli, Fatma Abdelhedi, Amal Souissi
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Background 8q21.11 microdeletion syndrome is a rare chromosomal disorder characterized by recurrent dysmorphic features, a variable degree of intellectual disability and ocular, cardiac and hand/feet abnormalities. To date, ZFHX4 is the only candidat