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The heart in congenital diaphragmatic hernia: Knowns, unknowns, and future priorities

Current Oncology, Vol. 29, Pages 5748-5762: The Use of Assisted Reproductive Technology by European Childhood Cancer Survivors

Nutrients, Vol. 14, Pages 1671: Optimal Nutrition Parameters for Neonates and Infants with Congenital Heart Disease

CHD4 is recruited by GATA4 and NKX2-5 to repress noncardiac gene programs in the developing heart [Research Papers]

Perioperative Use of Pituitrin after Cardiac Defect Repair in Adult Patients with Severe Pulmonary Hypertension

Diagnostics, Vol. 12, Pages 1917: Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

Dilated left ventricle with multiple outpouchings - a severe congenital ventricular diverticulum or left-dominant arrhythmogenic cardiomyopathy: A case report

Life, Vol. 12, Pages 1223: Outcome after Prenatal Diagnosis of Trisomy 13, 18, and 21 in Fetuses with Congenital Heart Disease

Pediatric Heart Failure Inpatient Mortality: A Cross-Sectional Analysis

Fluid Mechanics of Fetal Left Ventricle During Aortic Stenosis with Evolving Hypoplastic Left Heart Syndrome

Diagnostics, Vol. 11, Pages 1505: Magnetic Resonance Detects Structural Heart Disease in Patients with Frequent Ventricular Ectopy and Normal Echocardiographic Findings

IJERPH, Vol. 19, Pages 709: Muscle-Skeletal Abnormalities and Muscle Oxygenation during Isokinetic Strength Exercise in Heart Failure with Preserved Ejection Fraction Phenotype: A Cross-Sectional Study

Relationships among norepinephrine levels, exercise capacity, and chronotropic responses in heart failure patients

Skeletal muscle abnormalities in heart failure with preserved ejection fraction

Dual Specific Phosphatase 7 Exacerbates Dilated Cardiomyopathy, Heart Failure, and Cardiac Death by Inactivating the ERK1/2 Signaling Pathway

JCDD, Vol. 9, Pages 181: Complementary Role of Combined Indirect and Direct Cardiac Sympathetic (Hyper)Activity Assessment in Patients with Heart Failure by Spectral Analysis of Heart Rate Variability and Nuclear Imaging: Possible Application in the

Perimyocarditis With Acute Heart Failure as the First Manifestation of Systemic Lupus Erythematosus

074 No valvular heart disease or pulmonary artery hypertension with fenfluramine for up to 3 years

cfDNA in maternal blood and Artificial Intelligence: Accurate Prenatal Detection of Fetal Congenital Heart Defects

Anomalous Connection of the Left Pulmonary Vein to the Coronary Sinus with Intact Atrial Septum in a Young Woman

IJERPH, Vol. 19, Pages 9774: Why Is Health Care for Children with Down Syndrome so Crucial from the First Days of Life? A Retrospective Cohort Study Emphasized Transient Abnormal Myelopoiesis (TAM) Syndrome at Three Centers

IJERPH, Vol. 19, Pages 9774: Why Is Health Care for Children with Down Syndrome so Crucial from the First Days of Life? A Retrospective Cohort Study Emphasized Transient Abnormal Myelopoiesis (TAM) Syndrome at Three Centers

Synnynnäinen sydänvika - noninvasiivinen kuvantaminen seurannassa

Congenital Heart Defects in Ecuador: Population-Based Study and Demography Issues from 2000 to 2017

<em>SORBS2</em> is a genetic factor contributing to cardiac malformation of 4q deletion syndrome patients

Synnynnäinen sydänvika ja raskaus (Katsaus)

Study finds key protein related to the disease-causing malformation of fat tissue

Heart rate variability in the evaluation of the autonomic nervous system of premature infants

Prenatal detection of univentricular heart and transposition of the great arteries in Finland

Congenital diaphragmatic hernia with heart defect has a high risk for hypoplastic left heart syndrome and major extra-cardiac malformations - 10-year national cohort from Finland.

Congenital diaphragmatic hernia with heart defect has a high risk for hypoplastic left heart syndrome and major extra-cardiac malformations - 10-year national cohort from Finland.

Congenital diaphragmatic hernia with heart defect has a high risk for hypoplastic left heart syndrome and major extra-cardiac malformations: 10-year national cohort from Finland

Congenital heart defects in patients with isolated microtia: evaluation using colour Doppler echocardiographic image.

Congenital Constriction Band Syndrome With Limb Defects. A Population-based Study.

Neonatal Outcomes in Very Preterm Infants With Severe Congenital Heart Defects: An International Cohort Study.

Congenital heart diseases trends in São Paulo State, Brazil: a national live birth data bank analysis

Peters'-plus syndrome is a congenital disorder of glycosylation caused by a defect in the beta1,3-glucosyltransferase that modifies thrombospondin type 1 repeats.

Neonatal Outcomes in Very Preterm Infants With Severe Congenital Heart Defects: An International Cohort Study

Pathology and Advanced Imaging—Characterization of a Congenital Cardiac Defect and Complex Hemodynamics in a Pig: A Case Report

Congenital heart disease risk loci identified by genome-wide association study in European patients

Birth prevalence of congenital anomalies in Argentina, according to socioeconomic level

Maternal Smoking and Congenital Heart Defects, National Birth Defects Prevention Study, 1997-2011

Heart Failure Associated With Ventricular Septal Defect, Mitral Valve Prolapse, Non-stenotic Bicuspid Aortic Valve, and Patent Foramen Ovale

Congenital Heart Defects and the Risk of Spontaneous Preterm Birth