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Aortic flow patterns and wall shear stress maps by 4D-flow cardiovascular magnetic resonance in the assessment of aortic dilatation in bicuspid aortic valve disease

Journal of cardiovascular magnetic resonance, 2018-04, Vol.20 (1), p.28-28, Article 28

2018

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Efficacy of losartan vs. atenolol for the prevention of aortic dilation in Marfan syndrome: a randomized clinical trial

European heart journal, 2016-03, Vol.37 (12), p.978-985

2016

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False lumen rotational flow and aortic stiffness are associated with aortic growth rate in patients with chronic aortic dissection of the descending aorta: a 4D flow cardiovascular magnetic resonance study

Journal of cardiovascular magnetic resonance, 2022-03, Vol.24 (1), p.20-20, Article 20

2022

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European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

Orphanet journal of rare diseases, 2019-11, Vol.14 (1), p.264-264, Article 264

2019

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Three-dimensional aortic geometry mapping via registration of non-gated contrast-enhanced or gated and respiratory-navigated MR angiographies

Journal of cardiovascular magnetic resonance, 2024-01, Vol.26 (1), p.100992-100992

2024

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Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

Clinica chimica acta, 2014-11, Vol.437, p.88-92

2014

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Diagnostic value of quantitative parameters for myocardial perfusion assessment in patients with suspected coronary artery disease by single- and dual-energy computed tomography myocardial perfusion imaging

International journal of cardiology. Heart & vasculature, 2021-02, Vol.32, p.100721, Article 100721

2021

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Thoracic Aortic Volume as a Predictor of Cardiovascular Events: The Multi‐Ethnic Study of Atherosclerosis

Journal of magnetic resonance imaging, 2023-11

2023

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Proximal aorta longitudinal strain predicts aortic root dilation rate and aortic events in Marfan syndrome

European heart journal, 2019-07, Vol.40 (25), p.2047-2055

2019

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Multimodality Assessment of Ascending Aortic Diameters: Comparison of Different Measurement Methods

Journal of the American Society of Echocardiography, 2016-09, Vol.29 (9), p.819-826.e4

2016

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Prognosis of Paradoxical Low-Flow Low-Gradient Aortic Stenosis: A Severe, Non-critical Form, With Surgical Treatment Benefits

Frontiers in cardiovascular medicine, 2022-04, Vol.9, p.852954-852954

2022

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Altered DNA methylation indicates an oscillatory flow mediated epithelial-to-mesenchymal transition signature in ascending aorta of patients with bicuspid aortic valve

Scientific reports, 2018-02, Vol.8 (1), p.2777-15, Article 2777

2018

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Unraveling Bicuspid Aortic Valve Enigmas by Multimodality Imaging: Clinical Implications

Journal of clinical medicine, 2022-01, Vol.11 (2), p.456

2022

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Are Aortic Root and Ascending Aorta Diameters Measured by the Pediatric versus the Adult American Society of Echocardiography Guidelines Interchangeable?

Journal of clinical medicine, 2021-11, Vol.10 (22), p.5290

2021

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Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials

The Lancet (British edition), 2022-09, Vol.400 (10355), p.822-831

2022

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Familial clustering of bicuspid aortic valve and its relationship with aortic dilation in first-degree relatives

Heart (British Cardiac Society), 2019-04, Vol.105 (8), p.603

2019

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Allopurinol blocks aortic aneurysm in a mouse model of Marfan syndrome via reducing aortic oxidative stress

Free radical biology & medicine, 2022-11, Vol.193 (Pt 2), p.538-550

2022

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Implications of Asymmetry and Valvular Morphotype on Echocardiographic Measurements of the Aortic Root in Bicuspid Aortic Valve

Journal of the American Society of Echocardiography, 2019-01, Vol.32 (1), p.105-112

2019

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Sudden Cardiovascular Death in Young Patients With Aortic Dissection. What Lessons Should We Learn?

Revista española de cardiología (English ed.), 2019-07, Vol.72 (7), p.528-530

2019

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Heterogeneity of aortic disease severity in patients with Loeys–Dietz syndrome

Heart (British Cardiac Society), 2016-04, Vol.102 (8), p.626-632

2016

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Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study

European journal of medical genetics, 2022-06, Vol.65 (6), p.104503-104503, Article 104503

2022

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HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN

European journal of medical genetics, 2023-01, Vol.66 (1), p.104673-104673, Article 104673

2023

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Registration-based semi-automatic assessment of aortic diameter growth rate from contrast-enhanced computed tomography outperforms manual quantification

European radiology, 2022-03, Vol.32 (3), p.1997-2009

2022

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Enfermedad aórtica familiar no sindrómica: una entidad infradiagnosticada

Revista española de cardiologia, 2014-10, Vol.67 (10), p.861-863

2014

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Oral Presentation No. 121 Aortic stiffness descriptors by cardiac magnetic resonance are correlated with mechanical testing of ex-vivo aortic aneurysms specimens

Cardiovascular research, 2022-10, Vol.118 (Supplement_2)

2022

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Aortic flow patterns and wall shear stress maps by 4D-flow cardiovascular magnetic resonance in the assessment of aortic dilatation in bicuspid aortic valve disease

Efficacy of losartan vs. atenolol for the prevention of aortic dilation in Marfan syndrome: a randomized clinical trial

False lumen rotational flow and aortic stiffness are associated with aortic growth rate in patients with chronic aortic dissection of the descending aorta: a 4D flow cardiovascular magnetic resonance study

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

Three-dimensional aortic geometry mapping via registration of non-gated contrast-enhanced or gated and respiratory-navigated MR angiographies

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

Diagnostic value of quantitative parameters for myocardial perfusion assessment in patients with suspected coronary artery disease by single- and dual-energy computed tomography myocardial perfusion imaging

Thoracic Aortic Volume as a Predictor of Cardiovascular Events: The Multi‐Ethnic Study of Atherosclerosis

Proximal aorta longitudinal strain predicts aortic root dilation rate and aortic events in Marfan syndrome

Multimodality Assessment of Ascending Aortic Diameters: Comparison of Different Measurement Methods

Prognosis of Paradoxical Low-Flow Low-Gradient Aortic Stenosis: A Severe, Non-critical Form, With Surgical Treatment Benefits

Altered DNA methylation indicates an oscillatory flow mediated epithelial-to-mesenchymal transition signature in ascending aorta of patients with bicuspid aortic valve

Unraveling Bicuspid Aortic Valve Enigmas by Multimodality Imaging: Clinical Implications

Are Aortic Root and Ascending Aorta Diameters Measured by the Pediatric versus the Adult American Society of Echocardiography Guidelines Interchangeable?

Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials

Familial clustering of bicuspid aortic valve and its relationship with aortic dilation in first-degree relatives

Allopurinol blocks aortic aneurysm in a mouse model of Marfan syndrome via reducing aortic oxidative stress

Implications of Asymmetry and Valvular Morphotype on Echocardiographic Measurements of the Aortic Root in Bicuspid Aortic Valve

Sudden Cardiovascular Death in Young Patients With Aortic Dissection. What Lessons Should We Learn?

Heterogeneity of aortic disease severity in patients with Loeys–Dietz syndrome

Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study

HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN

Registration-based semi-automatic assessment of aortic diameter growth rate from contrast-enhanced computed tomography outperforms manual quantification

Enfermedad aórtica familiar no sindrómica: una entidad infradiagnosticada

Oral Presentation No. 121 Aortic stiffness descriptors by cardiac magnetic resonance are correlated with mechanical testing of ex-vivo aortic aneurysms specimens

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