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pro vyhledávání: '"S. Chabrak"'
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Autor:
Selma Charfeddine, W. Sdiri, M. Hassine, Sana Ouali, M.A. Mghaieth, A. Ben Halima, S. Chabrak, Z. Jabbari, E. Allouche, L. Zakhama, Leila Abid, Y. Messoudi, A. Haggui, K. Sayahi, H. Ajmi
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 12:125-126
Introduction Chronic kidney disease (CKD) has been related to poor quality of anticoagulation and an increased risk of bleeding. This study aims to evaluate the association between impaired renal function (eGFR Methods This is an ancillary analysis o
Autor:
S. Milouchi, Leila Abid, M. Ben Halima, M. Hassine, Selma Charfeddine, Y. Messoudi, S. Chabrak, K. Battikh, N. Larbi, S. Wali, F. Addad, Salma Krichène, Sami Mourali, A. Ben Halima, A. Haggui
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 12:124
Introduction Identifying patients who are likely to achieve and maintain a therapeutic international normalized ratio when prescribed a vitamin K antagonist (VKA) for stroke prevention in atrial fibrillation (AF) is challenging. The SAMe-TT2R2 score
Autor:
Sonia Marrakchi, Manel Ben Halima, Mohamed Ben Mbarek, Leila Abid, Rafik Chettaoui, H. Drissa, L. Zakhama, A. Haggui, Wajih Smati, Nadia Baraket, Sana Ouali, Soraya Ben Youssef, Gouider Jeridi, S. Chabrak, Salem Kachboura, Helmi Kammoun, Hedi Baccar, Samir Kammoun, Skander Ben Omrane, Habib Gamra, Najeh Ben Halima, Salem Abdesselem, Wided Nasraoui, Faouzi Maatouk, Ali Gasmi, Salma Krichène, Afef Ben Halima, Ali Neji, K. Sayahi, Sondes Kraiem, Rim Chrigui, Mohamed Fahmi Abbes, N. Larbi, Habib Haouala, W. Sdiri, F. Addad, Ines Issa, Slim Kacem, S. Milouchi, Youssef Harrath, Mohamed Rachid Boujnah, Samir Tlili, Essia Boughzala, Ali Ben Khalfallah, Mohamed Sami Mourali, Abdallah Mahdhaoui
Publikováno v:
JMIR Research Protocols
Background Atrial fibrillation (AF) is an important health problem in Tunisia. A significant change in the epidemiological pattern of heart disease has been seen in the last 3 decades; however, no large prospective multicenter trial reflecting nation
Publikováno v:
Annales de Cardiologie et d'Angéiologie. 55:241-245
Resume La letalite de l'infarctus du myocarde depend de plusieurs facteurs inherents au patient, a la maladie et sa severite ainsi qu'a la nature et la rapidite de la prise en charge. La revascularisation interventionnelle a prouve sa superiorite par
Autor:
G Jeridi, B. Tabarki, H. Ammar, Abdallah Mahdhaoui, B. Trimeche, Hatem Bouraoui, S. Chabrak, M.E Majdoub, S. Ernez-Hajri, N. Mahdhaoui
Publikováno v:
Acta Clinica Belgica. 58:54-57
Familial hypertrophic cardiomyopathy (HCM) with Wolff-Parkinson-White (WPW) syndrome is extremely rare and associated with a high risk of ventricular tachyarrhythmia and sudden death. We report a familial form of hypertrophic cardiomyopathy associate
Publikováno v:
Archives des maladies du coeur et des vaisseaux. 99(12)
We report two cases of celiac disease (CD) presented as an idiopathic dilated cardiomyopathy in association with a complete heart block in one patient, without digestive manifestation. The diagnosis of CD was obtained by both positivity of antiendomy
Publikováno v:
Annales de cardiologie et d'angeiologie. 55(5)
Acute myocardial infarction prognosis depends on many factors relative to the patient, to the disease and to the quality and promptness of the treatment. The interventional revascularisation is superior to pharmacological revascularisation. The aim o
Autor:
S, Chabrak, S, Ammar, N, Ammar, S, Ouali, F, Mghaieth, N, Larbi, N, Kafsi, F, Hentati, R, Mechmeche
Publikováno v:
La Tunisie medicale. 84(6)
Emery Dreifuss muscular dystrophy (EDMD) is an uncommon hereditary myopathy characterized by 3 symptoms: slow progressive muscular atrophy, muscular contractures and cardiac disease which affect prognosis. We report a 22 year-old patient with EDMD wh
Autor:
A, Mahdhaoui, H, Bouraoui, B, Tabarki, M, Majdoub, B, Trimeche, N, Mahdhaoui, S, Chabrak, S, Ernez-Hajri, G, Jeridi, H, Ammar
Publikováno v:
Acta clinica Belgica. 58(1)
Familial hypertrophic cardiomyopathy (HCM) with Wolff-Parkinson-White (WPW) syndrome is extremely rare and associated with a high risk of ventricular tachyarrhythmia and sudden death. We report a familial form of hypertrophic cardiomyopathy associate