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Mutational analysis using next-generation sequencing in sporadic and familial congenital heart disease

30 August 2016 (17:51 - 18:00)
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Congress Presentation Part of: Cutting edge research in congenital heart disease Morphology, pathology and genetics ESC Premium Access ESC Congress 2016

About the speaker

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Ms Silvia Pulignani

Institute of Clinical Physiology (IFC), Pisa (Italy)

9 More presentations in this session

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Observer variability in the assessment of congenital coronary abnormalities by invasive and CT coronary angiography: substudy of the anomalous connections of the coronary arteries (ANOCOR) registry
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Cardiac CT to evaluate risk of coronary compression in candidate patients for percutaneous pulmonary valve implantation
Miss M. Tezza (Verona, IT)
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Risks of pregnancy in women with rheumatic mitral valve disease: data from ROPAC, an ESC registry.
Ms I. van Hagen (Rotterdam, NL)
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Thromboembolic complications in adults fontan patients with atrial arrhythmia
Doctor A. Egbe (Rochester, US)
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Catheter-based right ventricle outflow tract procedures versus systemic-to-pulmonary shunts for initial palliation in infants with tetralogy of Fallot
Doctor D. Dorobantu (Bristol, GB)
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Access the full session

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Cutting edge research in congenital heart disease

The Event

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ESC Congress 2016

30 August 2016 17:51 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources