Detalhe da pesquisa
1.
Angiotensin receptor blockers and ß blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials.
Lancet
; 400(10355): 822-831, 2022 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36049495
2.
Unsuspected somatic mosaicism for FBN1 gene contributes to Marfan syndrome.
Genet Med
; 23(5): 865-871, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495528
3.
Clinical relevance of genotype-phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants.
Genet Med
; 23(7): 1296-1304, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33731877
4.
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Genet Med
; 23(1): 111-122, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32855533
5.
Staged hybrid repair of type II thoracoabdominal aneurysms.
J Vasc Surg
; 74(1): 20-27, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33340705
6.
Cardiovascular Magnetic Resonance May Avoid Unnecessary Coronary Angiography in Patients With Unexplained Left Ventricular Systolic Dysfunction: A Retrospective Diagnostic Pilot Study.
J Card Fail
; 26(12): 1067-1074, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-32942010
7.
There is insufficient evidence to lower the threshold for prophylactic aortic surgery.
Eur Heart J
; 45(8): 632, 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37936302
8.
Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD).
Genet Med
; 21(9): 2015-2024, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30739908
9.
False lumen embolization in chronic aortic dissection promotes thoracic aortic remodeling at midterm follow-up.
J Vasc Surg
; 70(3): 710-717, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30850289
10.
Red Blood Cell Scintigraphy and the Controversy of Endotension After Aortic Aneurysm Endovascular Repair.
Eur J Vasc Endovasc Surg
; 67(1): 173-174, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37832910
11.
Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome.
J Med Genet
; 54(2): 100-103, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27582083
12.
MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections.
Am J Hum Genet
; 95(6): 736-43, 2014 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-25434006
13.
Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg?
Eur Heart J
; 37(47): 3525-3531, 2016 Dec 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-26908951
14.
Preliminary Experience With Custom Made Hourglass Shaped Thoracic Stent Grafts for Endovascular Thoracic Aortic Coarctation Repair in Adults.
Eur J Vasc Endovasc Surg
; 62(6): 1000-1001, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34627679
15.
Marfan sartan saga, episode X.
Eur Heart J
; 41(43): 4188-4190, 2020 11 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-32607591
16.
Marfan Sartan: a randomized, double-blind, placebo-controlled trial.
Eur Heart J
; 36(32): 2160-6, 2015 Aug 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-25935877
17.
Incidence, diagnostic methods, and evolution of left ventricular thrombus in patients with anterior myocardial infarction and low left ventricular ejection fraction: a prospective multicenter study.
Am Heart J
; 170(2): 256-62, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26299222
18.
Aortic event rate in the Marfan population: a cohort study.
Circulation
; 125(2): 226-32, 2012 Jan 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-22133496
19.
Primary Non-Aortic Lesions Are Not Rare in Marfan Syndrome and Are Associated with Aortic Dissection Independently of Age.
J Clin Med
; 12(8)2023 Apr 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-37109238
20.
Multicentre medicoeconomic evaluation of cardiac magnetic resonance imaging for predicting coronary artery disease in left ventricular dysfunction: The CAMAREC study design.
Arch Cardiovasc Dis
; 116(8-9): 366-372, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37573160