Publications by authors named "Fatma Ourda"

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Dilated Cardiomyopathy due to the Novel Missense Mutation m.14757T>C.
Sinda Zarrouk, Josef Finsterer, Sounira Mehri, Fatma Ourda, Saida Ben Arab

J Med Cases· November 2021

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46th Medical Maghrebian Congress. November 9-10, 2018. Tunis.
A Alami Aroussi, A Fouad, A Omrane, A Razzak, A Aissa, Fatma Ourda

Tunis Med· January 2019

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Epidemiology and outcome of primary cardiac tumours prenatally, in neonatesneonnates and children: A single center experience from tunis.
Hela Msaad, Meriem Drissa, Khaouther Hakim, Fatma Ourda

Egypt Heart J· December 2018

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Pathogenicity of the transition m.3308T>C in left ventricular hypertrabeculation/noncompaction.
Sinda Zarrouk Mahjoub, Sounira Mehri, Fatma Ourda, Rafik Boussaada, Rachid Mechmeche

Cardiology· November 2012

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Novel m.15434C>A (p.230L>I) Mitochondrial Cytb Gene Missense Mutation Associated with Dilated Cardiomyopathy.
Sinda Zarrouk Mahjoub, Sounira Mehri, Fatma Ourda, Josef Finsterer, Saïda Ben Arab

ISRN Cardiol· August 2012

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Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction.
Sinda Zarrouk Mahjoub, Sounira Mehri, Fatma Ourda, Rafik Boussaada, Rachid Mechmeche

Cardiology· December 2011

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