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The finding of a founder mutation c.3344C>T(p.Pro1115Leu) in EIF2KA4 gene in iberian romani patients with pulmonary veno-occlusive disease: a family matter.

30 August 2016 (15:20 - 15:30)
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Congress Presentation Part of: Pulmonary hypertension: diagnosis, functional imaging and molecular phenotyping Chronic pulmonary hypertension ESC Premium Access ESC Congress 2016

About the speaker

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Doctor Carlos Andres Quezada-Loaiza

University Hospital 12 de Octubre, Madrid (Spain)

8 More presentations in this session

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Brain natriuretic peptide (BNP) level at enrolment predicts 1- and 5-year transplant-free survival in patients with pulmonary arterial hypertension (PAH): data from the REVEAL registry
Doctor R. Frantz (Rochester, US)
Abstract Slides Video
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Severe ventricular interdependence as a cause of misclassification of group 2 pulmonary hypertension
Doctor S. Rosset (Lausanne, CH)
Abstract Slides Video
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Pulmonary hypertension and pregnancy outcomes: data from the ropac study of the european society of cardiology
Doctor I. van Hagen (Rotterdam, NL)
Abstract Slides Video
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Left and right ventricular peak filling rates are reduced in patients with pulmonary arterial hypertension measured with magnetic resonance imaging
Doctor C. Goransson (Malmo, SE)
Abstract Slides Video
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Peak oxygen uptake during exercise is able to exclude scleroderma-associated pulmonary arterial hypertension with a high probability
Doctor D. Dumitrescu (Bad Oeynhausen, DE)
Abstract Slides Video

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Pulmonary hypertension: diagnosis, functional imaging and molecular phenotyping

The Event

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ESC Congress 2016

30 August 2016 15:20 CET

ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources