Cardiac arrhythmias and genetics

Unmasking immune reconstitution inflammatory syndrome: a report of tuberculous epididymo-orchitis mimicking a testicular tumour in a Caucasian AIDS patient.

International journal of STD & AIDS·2016

World wide web and scientific publishing.

Images in paediatric cardiology·2012

Atrial septal defect: spectrum of care.

Pediatric cardiology·2007

Aortic stenosis: the spectrum of practice.

Pediatric cardiology·2006

Hybrid pediatric cardiac surgery.

Pediatric cardiology·2005

Multicenter experience with perventricular device closure of muscular ventricular septal defects.

Pediatric cardiology·2005

Factors Influencing Weight Gain at Different Stages of the Fontan Pathway for Children with Functionally Single Ventricle Heart Disease.

Pediatric cardiology·2026

The Right Atrium and Atrialised Right Ventricle are Associated with Cardiac Output During Exercise in Patients with Ebstein Anomaly of the Tricuspid Valve.

Pediatric cardiology·2026

Myocardial Deformation Analysis in Congenital Aortic Valve Stenosis: Comparison Across Clinical Phenotypes in Children.

Pediatric cardiology·2026

Bedside Ultrasound and Noninvasive Cardiac Output Monitoring in Children with Septic Shock: A Retrospective Comparative Study.

Pediatric cardiology·2026

Outcome of Patients with Single Ventricles who Initially did not Indicate Fontan Completion After Stage II Palliation.

Pediatric cardiology·2026

Outcomes of Congenital Heart Disease Deliveries at a Freestanding Children's Hospital.

Pediatric cardiology·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

Cardiac arrhythmias and genetics

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Unmasking immune reconstitution inflammatory syndrome: a report of tuberculous epididymo-orchitis mimicking a testicular tumour in a Caucasian AIDS patient.

World wide web and scientific publishing.

Atrial septal defect: spectrum of care.

Aortic stenosis: the spectrum of practice.

Hybrid pediatric cardiac surgery.

Multicenter experience with perventricular device closure of muscular ventricular septal defects.

Factors Influencing Weight Gain at Different Stages of the Fontan Pathway for Children with Functionally Single Ventricle Heart Disease.

The Right Atrium and Atrialised Right Ventricle are Associated with Cardiac Output During Exercise in Patients with Ebstein Anomaly of the Tricuspid Valve.

Myocardial Deformation Analysis in Congenital Aortic Valve Stenosis: Comparison Across Clinical Phenotypes in Children.

Bedside Ultrasound and Noninvasive Cardiac Output Monitoring in Children with Septic Shock: A Retrospective Comparative Study.

Outcome of Patients with Single Ventricles who Initially did not Indicate Fontan Completion After Stage II Palliation.

Outcomes of Congenital Heart Disease Deliveries at a Freestanding Children's Hospital.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Related Experiment Videos

Cardiac arrhythmias and genetics

Related Concept Videos

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