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Autor: Dany Minetto, Tornike Sologashvili, Anne-Lise Hachulla, Philippe Meyer, C Blanche

Publikováno v: JACC Case Reports
JACC: Case Reports, Vol 2, Iss 2, Pp 261-265 (2020)

A 38-year-old asymptomatic man was referred by his general practitioner for a 3/6 systolic heart murmur, which was detected during a routine consultation. Echocardiography revealed a parachute mitral valve associated with a parachute-like membrane, c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb635b175ba79720dfdd08abf325a56f
http://europepmc.org/articles/PMC8298313

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Akademický článek

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2D cine vs. 3D self-navigated free-breathing high-resolution whole heart cardiovascular magnetic resonance for aortic root measurements in congenital heart disease

Autor: Clement Nussbaumer, Matthias Stuber, Jürg Schwitter, Davide Piccini, C Blanche, Pierre Monney, Anna-Giulia Pavon, Tobias Rutz, Judith Bouchardy

Publikováno v: Journal of Cardiovascular Magnetic Resonance
Journal of Cardiovascular Magnetic Resonance, Vol 23, Iss 1, Pp 1-12 (2021)

Background Cardiovascular magnetic resonance (CMR) is considered the method of choice for evaluation of aortic root dilatation in congenital heart disease. Usually, a cross-sectional 2D cine stack is acquired perpendicular to the vessel’s axis. How

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dfcd5b7e8e40b80fce4956a81547c45
https://doi.org/10.1186/s12968-021-00744-1

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Evolution of biventricular T1 values in patients with right-sided congenital heart disease

Autor: C Blanche, Tobias Rutz, Pierre Monney, Judith Bouchardy, Jürg Schwitter, Anna Giulia Pavon, O Burdet, S Hugelshofer

Publikováno v: European Heart Journal - Cardiovascular Imaging. 22

Funding Acknowledgements Type of funding sources: None. Background Conflicting reports exist on the prevalence and clinical impact of interstitial fibrosis in right ventricular (RV) congenital heart disease (CHD). This study evaluates the longitudina

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c70f45f054d92f685bde71ad03deed41
https://doi.org/10.1093/ehjci/jeaa356.405

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2D cine vs. 3D free-breathing self-navigated whole heart for aortic root measurements in congenital heart disease

Autor: Matthias Stuber, S Hugelshofer, Judith Bouchardy, C Nussbaumer, Anna Giulia Pavon, D Piccini, Pierre Monney, Tobias Rutz, Jürg Schwitter, C Blanche

Publikováno v: European Heart Journal - Cardiovascular Imaging. 22

Funding Acknowledgements Type of funding sources: None. Background Cardiac magnetic resonance is considered the method of choice for determination of aortic root diameters in congenital heart disease. Usually, a cross-sectional 2D cine stack is acqui

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::84e66c728facb109fe5d71f6d378a8d4
https://doi.org/10.1093/ehjci/jeaa356.404

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Prevalence of arrhythmias on the long term of adult patients with partial anomalous pulmonary venous connection treated surgically and conservatively: data from the SACHER registry and a French center

Autor: G Harald, Tobias Rutz, M Touray, R Engel, Magalie Ladouceur, Matthias Greutmann, Judith Bouchardy, Markus Schwerzmann, Daniel Tobler, C Blanche, N. Sekarski, Etienne Pruvot

Publikováno v: European Heart Journal. 41

Introduction Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital heart disease, characterized by one or some but not all pulmonary veins anomalously connected to the right atrium or a systemic vein. PAPVC is either an isolated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9030948bc7349b377a33f81ef5aa6ca5
https://doi.org/10.1093/ehjci/ehaa946.2204

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Long-term outcome of adult patients with total anomalous pulmonary venous connection: data from the SACHER registry and a French center

Autor: C Blanche, Magalie Ladouceur, N. Sekarski, G Harald, Markus Schwerzmann, Judith Bouchardy, M Touray, Daniel Tobler, Tobias Rutz, Matthias Greutmann, R Engel, Etienne Pruvot

Publikováno v: European Heart Journal. 41

Introduction Total anomalous pulmonary venous connection is a rare cyanotic congenital heart disease, where all pulmonary veins aberrantly connect to a systemic vein or the right atrium. The only curative treatment is surgery allowing the patients to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7fa4661bbfb877dc8a7518e81f3de9b3
https://doi.org/10.1093/ehjci/ehaa946.2172

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Long-term outcome of adult patients with partial anomalous pulmonary venous connection treated surgically and conservatively: data from the SACHER registry and a French center

Autor: M Touray, Tobias Rutz, R Engel, Magalie Ladouceur, Daniel Tobler, Etienne Pruvot, Matthias Greutmann, C Blanche, Judith Bouchardy, N. Sekarski, R Harald, Markus Schwerzmann

Publikováno v: European Heart Journal. 41

Introduction Partial anomalous pulmonary venous connection (PAPVC) is a rare congenital heart disease, which is characterized by one or some but not all pulmonary veins anomalously connected to the right atrium or a systemic vein. PAPVC is either an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2463190d8d981ecebca5d146738b706f
https://doi.org/10.1093/ehjci/ehaa946.2222

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