Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).
about
Surgical treatment of patients enrolled in the national registry of genetically triggered thoracic aortic conditions.The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): results from phase I and scientific opportunities in phase II.Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry.Molecular imaging of aortic aneurysms.Bicuspid aortic valve and thoracic aortic aneurysm: three patient populations, two disease phenotypes, and one shared genotype.The Need for Standardized Methods for Measuring the Aorta: Multimodality Core Lab Experience From the GenTAC Registry.Valve-sparing aortic root replacement in patients with Marfan syndrome enrolled in the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions.Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).Aortic Dissection in Patients With Genetically Mediated Aneurysms: Incidence and Predictors in the GenTAC Registry.Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC) registry predicting predictors for aortic dissection: a new thought around the corner?Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome.Genetic biomarkers in aortopathy.Bicuspid and unicuspid aortic valves: Different phenotypes of the same disease? Insight from the GenTAC Registry.Aortic Dilatation Associated With Bicuspid Aortic Valve: Relation to Sex, Hemodynamics, and Valve Morphology (the National Heart Lung and Blood Institute-Sponsored National Registry of Genetically Triggered Thoracic Aortic Aneurysms and CardiovasculMarfan Syndrome and Quality of Life in the GenTAC Registry.Pathophysiology of aortic aneurysm: insights from human genetics and mouse models.Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry.Systematic review and meta-analysis of surgical outcomes in Marfan patients undergoing aortic root surgery by composite-valve graft or valve sparing root replacement.Notch1 haploinsufficiency causes ascending aortic aneurysms in mice.GenTAC registry report: gender differences among individuals with genetically triggered thoracic aortic aneurysm and dissection
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P2860
Rationale and design of the National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC).
description
2008 nî lūn-bûn
@nan
2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@ast
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@en
type
label
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@ast
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@en
prefLabel
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@ast
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@en
P2860
P1476
Rationale and design of the Na ...... ovascular Conditions (GenTAC).
@en
P2093
GenTAC Consortium
Kim A Eagle
P2860
P304
P356
10.1016/J.AHJ.2008.10.005
P407
P577
2008-12-17T00:00:00Z