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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

American journal of human genetics, 2014-12, Vol.95 (6), p.736-743

2014

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Inhibition of Glycoprotein VI Clustering by Collagen as a Mechanism of Inhibiting Collagen-Induced Platelet Responses: The Example of Losartan

PloS one, 2015-06, Vol.10 (6), p.e0128744-e0128744

2015

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Publisher Correction: Marfan syndrome

Nature reviews. Disease primers, 2022-01, Vol.8 (1), p.3-3, Article 3

2022

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Beta-Blockers in Acute Heart Failure

JACC. Heart failure, 2015-08, Vol.3 (8), p.654-656

2015

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Optimizing Aortic Endovascular Repair in Patients with Marfan Syndrome

European journal of vascular and endovascular surgery, 2019-12, Vol.58 (6), p.e763-e764

2019

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Effect of Serelaxin on Cardiac, Renal, and Hepatic Biomarkers in the Relaxin in Acute Heart Failure (RELAX-AHF) Development Program

Journal of the American College of Cardiology, 2013-01, Vol.61 (2), p.196-206

2013

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Hyperventilation as one of the mechanisms of persistent dyspnoea in SARS-CoV-2 survivors

The European respiratory journal, 2021-07, Vol.58 (2)

2021

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False Lumen Embolization in Chronic Aortic Dissections to Improve Results of Thoracic Endovascular Aortic Repair: Early Experience of 21 Consecutive Cases

European journal of vascular and endovascular surgery, 2019-12, Vol.58 (6), p.e3-e4

2019

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Intrathoracic Impedance Monitoring, Audible Patient Alerts, and Outcome in Patients With Heart Failure

Journal of cardiac failure, 2011, Vol.17 (11), p.972-972

2011

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Peripheral arterial lesions of Marfan’s the disease: Analysis of a multicentric 138 patients cohort

Annals of vascular surgery, 2022-08, Vol.84, p.79-80

2022

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TGFB3-RELATED HERITABLE THORACIC AORTIC DISEASE: RESULTS FROM THE MONTALCINO AORTIC CONSORTIUM

Journal of the American College of Cardiology, 2023-03, Vol.81 (8), p.2020-2020

2023

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Plasma Brain Natriuretic Peptide-Guided Therapy to Improve Outcome in Heart Failure

Journal of the American College of Cardiology, , Vol.49 (16), p.1733-1739

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Une filière maladies vasculaires rares (FAVAMulti) : pour quoi faire ?

Journal de médecine vasculaire, 2023-03, Vol.48, p.S37-S38

2023

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SIMPLE RENAL CYSTS AND AORTIC DISEASE IN MARFAN SYNDROME AND MATCHED CONTROLS

Journal of the American College of Cardiology, 2018-03, Vol.71 (11), p.A2064-A2064

2018

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UNEXPLAINED LEFT VENTRICULAR DYSFUNCTION: HOW IS CORONARY ANGIOGRAPHY USEFUL TODAY?

Journal of the American College of Cardiology, 2022-03, Vol.79 (9), p.423

2022

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Wall Activation of Plasminogen in Aortic Dissections and Aneurysms: an Experimental Model in the Rat for Preclinical Pharmacology

Annals of vascular surgery, 2018-11, Vol.53, p.23-23

2018

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Genotype-Mitral Valve Phenotype Correlations in Marfan Syndrome With FBN1 Pathogenic Variants

JACC. Advances (Online), 2022-12, Vol.1 (5), p.100149, Article 100149

2022

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Sequential orthotopic hybrid treatment of type 2 thoracoabdominal aneurysms

Annals of vascular surgery, 2020-10, Vol.68, p.114-115

2020

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Feasibility and accuracy of linking a heart failure registry to the national claims database using indirect identifiers

Archives of cardiovascular diseases, 2022-12, Vol.116 (1), p.18-24

2022

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Definition of a Protocol to Choose Thoracic Stentgrafts in Marfan’s Disease Patients Treated for Aortic Dissection: Preliminary Experience

Annals of vascular surgery, 2018-11, Vol.53, p.13-14

2018

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MARFAN SYNDROME RELATED TO TGFβR2 MUTATION AND SUDDEN DEATH: A ROLE FOR ABNORMAL VENTRICULAR REPOLARIZATION RELATED ARRHYTHMIAS?

Journal of the American College of Cardiology, 2016-04, Vol.67 (13), p.679-679

2016

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MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

Inhibition of Glycoprotein VI Clustering by Collagen as a Mechanism of Inhibiting Collagen-Induced Platelet Responses: The Example of Losartan

Early-onset osteoarthritis, Charcot-Marie-Tooth like neuropathy, autoimmune features, multiple arterial aneurysms and dissections: an unrecognized and life threatening condition

Publisher Correction: Marfan syndrome

Beta-Blockers in Acute Heart Failure

Optimizing Aortic Endovascular Repair in Patients with Marfan Syndrome

Effect of Serelaxin on Cardiac, Renal, and Hepatic Biomarkers in the Relaxin in Acute Heart Failure (RELAX-AHF) Development Program

Hyperventilation as one of the mechanisms of persistent dyspnoea in SARS-CoV-2 survivors

False Lumen Embolization in Chronic Aortic Dissections to Improve Results of Thoracic Endovascular Aortic Repair: Early Experience of 21 Consecutive Cases

Intrathoracic Impedance Monitoring, Audible Patient Alerts, and Outcome in Patients With Heart Failure

Peripheral arterial lesions of Marfan’s the disease: Analysis of a multicentric 138 patients cohort

TGFB3-RELATED HERITABLE THORACIC AORTIC DISEASE: RESULTS FROM THE MONTALCINO AORTIC CONSORTIUM

Plasma Brain Natriuretic Peptide-Guided Therapy to Improve Outcome in Heart Failure

Une filière maladies vasculaires rares (FAVAMulti) : pour quoi faire ?

SIMPLE RENAL CYSTS AND AORTIC DISEASE IN MARFAN SYNDROME AND MATCHED CONTROLS

UNEXPLAINED LEFT VENTRICULAR DYSFUNCTION: HOW IS CORONARY ANGIOGRAPHY USEFUL TODAY?

Wall Activation of Plasminogen in Aortic Dissections and Aneurysms: an Experimental Model in the Rat for Preclinical Pharmacology

Genotype-Mitral Valve Phenotype Correlations in Marfan Syndrome With FBN1 Pathogenic Variants

Sequential orthotopic hybrid treatment of type 2 thoracoabdominal aneurysms

Feasibility and accuracy of linking a heart failure registry to the national claims database using indirect identifiers

Rationale and design of the PACIFIC-PRESERVED (PhenomApping, ClassIFication and Innovation for Cardiac dysfunction in patients with heart failure and PRESERVED left ventricular ejection fraction) study

Definition of a Protocol to Choose Thoracic Stentgrafts in Marfan’s Disease Patients Treated for Aortic Dissection: Preliminary Experience

Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction

Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction

MARFAN SYNDROME RELATED TO TGFβR2 MUTATION AND SUDDEN DEATH: A ROLE FOR ABNORMAL VENTRICULAR REPOLARIZATION RELATED ARRHYTHMIAS?

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