Search Results - "Mesquita, Sonia M"
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Genetic and environmental risk factors in congenital heart disease functionally converge in protein networks driving heart development
Published in Proceedings of the National Academy of Sciences - PNAS (28-08-2012)“…Congenital heart disease (CHD) occurs in ∼1% of newborns. CHD arises from many distinct etiologies, ranging from genetic or genomic variation to exposure to…”
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NKX2.5 mutations in patients with non-syndromic congenital heart disease
Published in International journal of cardiology (04-02-2010)“…Abstract Background Cardiac development is a complex and multifactorial biological process. Heterozygous mutations in the transcription factor NKX2.5 are…”
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ALDH1A2 (RALDH2) genetic variation in human congenital heart disease
Published in BMC genetics (03-11-2009)“…Signaling by the vitamin A-derived morphogen retinoic acid (RA) is required at multiple steps of cardiac development. Since conversion of retinaldehyde to RA…”
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Atrial septal defect in adults: does repair always mean cure?
Published in Arquivos brasileiros de cardiologia (01-12-2014)Get full text
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Platelet protease-activated receptor 1 and membrane expression of P-selectin in pulmonary arterial hypertension
Published in Thrombosis research (01-01-2010)“…Abstract Introduction Pulmonary arterial hypertension (PAH) is frequently associated with thrombotic events, particularly involving the pulmonary…”
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Congenital heart disease and pulmonary arterial hypertension in South America (2013 Grover Conference series)
Published in Pulmonary Circulation (01-09-2014)“…South America is a territory of 17,819,100 km2, where ∼388 million people live in 13 countries. In the region, access to medical assistance (e.g., for…”
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Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design
Published in International journal of cardiology (20-10-2005)“…Hyperhomocysteinemia is frequently associated with congenital defects of the heart and neural tube. A common missense mutation in the MTHFR gene (C to T…”
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De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot
Published in Nature genetics (01-08-2009)“…Tetralogy of Fallot (TOF), the most common severe congenital heart malformation, occurs sporadically, without other anomaly, and from unknown cause in 70% of…”
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Likelihood of left main coronary artery compression based on pulmonary trunk diameter in patients with pulmonary hypertension
Published in The American journal of medicine (15-03-2004)“…In patients with pulmonary hypertension, extrinsic compression of the left main coronary artery by a dilated pulmonary trunk may cause angina, left ventricular…”
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Abstract 10210: Effects of Chronic Treatment With the Phosphodiesterase-5 Inhibitors Sildenafil and Tadalafil on Platelet Aggregation in Patients With Eisenmenger Syndrome
Published in Circulation (New York, N.Y.) (10-11-2015)“…BackgroundPatients with pulmonary arterial hypertension (PAH) associated with the Eisenmeger syndrome (ES) frequently have decreased platelet counts and…”
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Abstract 10323: Tadalafil Therapy Improves Endothelial Thrombomodulin in Hypoxemic Patients With Pulmonary Arterial Hypertension Associated With the Eisenmenger Syndrome
Published in Circulation (New York, N.Y.) (10-11-2015)“…IntroductionThrombomodulin (TM) is a plasma membrane chondroitin sulfate proteoglycan acting as a natural endothelial anticoagulant and anti-thrombotic factor…”
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Atrial septal defect in adults: does repair always mean cure?
Published in Arquivos brasileiros de cardiologia (01-12-2014)Get full text
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Atrial Septal Defect in Adults: Does Repair Always Mean Cure?
Published in Arquivos brasileiros de cardiologia (01-12-2014)Get full text
Journal Article -
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ALDH1A2
Published in BMC medical genetics (03-11-2009)“…Signaling by the vitamin A-derived morphogen retinoic acid (RA) is required at multiple steps of cardiac development. Since conversion of retinaldehyde to RA…”
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Journal Article