الرئيسية › دليل الباحثين › Fatma Ouarda

Fatma Ouarda

الانتماء : Tunis University · Hôpital La Rabta · Faculté de médecine de Tunis · Tunis El Manar University

• 31منشورات (انتماء تونسي)
• 53مجموع المنشورات
• 158الاستشهادات
• 8مؤشر h

OpenAlex

مجالات البحث

• Congenital Heart Disease Studies
• Cardiac electrophysiology and arrhythmias
• Cardiovascular Conditions and Treatments
• Cardiac Arrhythmias and Treatments
• Cardiomyopathy and Myosin Studies

المنشورات (31)

• Outcomes after Balloon Pulmonary Valvuloplasty for Critical Pulmonary Stenosis: A Tunisian reference center experience
  2026 · La Tunisie Médicale
• VSD Device Removal Due to Intermittent Complete Heart Block
  2026 · JACC Case Reports
• Identification of Biomarkers of Arrhythmogenic Cardiomyopathy (ACM) by Plasma Proteomics
  2025 · Medicina
• Challenging Percutaneous Extraction of an Intracardiac Implantable Chamber Catheter
  2025 · JACC Case Reports
• Assessment of ventricular function after total cavo-pulmonary derivation in adult patients: Interest of global longitudinal strain
  2023 · Journal of Cardiovascular and Thoracic Research · استُشهد به 3 مرة
• Paucisymptomatic Tetralogy of Fallot diagnosed in a 56-year-old patient: a case report
  2023 · The Egyptian Heart Journal · استُشهد به 2 مرة
• Double-Chambered Left Ventricle Diagnosed in Fetus and Follow-up During the First Year of Life: A Case Report
  2023 · World Journal for Pediatric and Congenital Heart Surgery · استُشهد به 1 مرة
• The yield of 24-hour ambulatory electrocardiography in the assessment of symptomatic school-age children.
  2023 · PubMed Central
• Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome
  2022 · Molecular Genetics & Genomic Medicine · استُشهد به 14 مرة
• Tétralogie de Fallot réparée au long terme : paramètres échographiques en corrélation avec l'IRM cardiaque
  2022 · Annales de Cardiologie et d Angéiologie · استُشهد به 1 مرة
• Anomalies cardiaques associées à l'hyperthyroïdie : étude clinique, structurelle et rythmique
  2022 · Annales de Cardiologie et d Angéiologie
• Transcatheter closure of silent patent ductus arteriosus for prevention of endocarditis is justified
  2021 · Archives of Cardiovascular Diseases Supplements · استُشهد به 1 مرة
• Electocardiographic features in Ebstein's disease
  2021 · Archives of Cardiovascular Diseases Supplements
• Interrupted aortic arch: Is it always a neonatal emergency?
  2021 · Archives of Cardiovascular Diseases Supplements
• P1004Diagnosis and management of fetal cardiac arrhythmias: about 100 cases
  2019 · European Heart Journal
• Contribution of imaging modalities in the diagnosis of middle aortic syndrome
  2018 · The Egyptian Heart Journal · استُشهد به 1 مرة
• Incidental Finding Of a Massive Cardiac Metastasis in a Boy Treated For a Parameningeal Rhabdomyosarcoma
  2018 · American Journal of Cardiovascular and Thoracic Surgery
• Cardiomyopathy induced by incessant ventricular tachycardia originating in the vicinity of the His bundle
  2017 · Indian Pacing and Electrophysiology Journal · استُشهد به 1 مرة
• Giant aortic arch aneurysm complicating Kawasaki′s disease
  2014 · Annals of Pediatric Cardiology · استُشهد به 11 مرة
• Interruption de l’arche sans canal artériel : la survie est-elle possible ?
  2014 · Archives de Pédiatrie
• Anomalous origin of the right coronary artery from the pulmonary artery. Two case reports
  2013 · The Egyptian Heart Journal · استُشهد به 12 مرة
• Successful pregnancy and delivery in a woman with a single ventricle and Eisenmenger syndrome
  2013 · Journal of the Saudi Heart Association · استُشهد به 10 مرة
• Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy
  2013 · Herz · استُشهد به 8 مرة
• Konno Ross procedure, coronary artery bypass graft and mitral valve replacement in a 12-year-old girl with homozygous familial hypercholesterolemia
  2013 · The Egyptian Heart Journal
• Long Term Outcome of Arterial Switch for Transposition of Great Arteries in Tunisian Children. First Experience in an Emergent Country
  2013 · Journal of the American College of Cardiology
• Infant-Type Anomalous Origin of the Left Coronary Artery From the Main Pulmonary Artery Diagnosed With Sixty-Four Multislice Computed Tomography
  2011 · Pediatric Cardiology · استُشهد به 2 مرة
• 251 Renin-angiotensin-aldosterone system polymorphisms: a role or a hole in occurrence and long-term prognosis of acute myocardial infarction at Tunisian older people
  2011 · Archives of Cardiovascular Diseases Supplements
• Association of ACE I/D polymorphism in Tunisian patients with dilated cardiomyopathy
  2010 · Journal of the Renin-Angiotensin-Aldosterone System · استُشهد به 21 مرة
• HLA class II polymorphisms in Tunisian patients with dilated cardiomyopathy
  2010 · Tissue Antigens · استُشهد به 11 مرة
• Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families
  2010 · Heart & Lung · استُشهد به 1 مرة
• [Atrial flutter in neonates and infants: diagnosis and treatment].
  2002 · PubMed · استُشهد به 2 مرة

مجلات النشر

• The Egyptian Heart Journal × 4
• Archives of Cardiovascular Diseases Supplements × 4
• JACC Case Reports × 2
• Annales de Cardiologie et d Angéiologie × 2
• La Tunisie Médicale × 1
• Medicina × 1

المنشورات حسب السنة

• 20262
• 20252
• 20234
• 20223
• 20213
• 20191
• 20182
• 20171
• 20142
• 20135

التعاون العلمي

المؤسسات الشريكة : University of Monastir · Institut Pasteur de Tunis · Hôpital Charles-Nicolle · Hôpital Farhat Hached · University of Sousse

المؤلفون المشاركون

• Kaouther Hakim
• Hela Msaad
• Rafik Boussaâda
• Rihab Ben Othmen
• Sinda Zarrouk‐Mahjoub
• Habiba Mizouni
• Sounira Mehri
• Kaouthar Hakim
• Rachid Mechmèche
• Mohamed Hammami
• Khalil Ouaghlani
• Ella Lehmayer

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).