Jacoba J. Louw

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 16 publications

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return.

Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return.

Journal: European journal of human genetics : EJHG

Published: April 27, 2023

Persistent Markers of Kidney Injury in Children Who Developed Acute Kidney Injury After Pediatric Cardiac Surgery: A Prospective Cohort Study.

Persistent Markers of Kidney Injury in Children Who Developed Acute Kidney Injury After Pediatric Cardiac Surgery: A Prospective Cohort Study.

Journal: Journal of the American Heart Association

Published: March 18, 2022

Percutaneous embolization of lymphatic fistulae as treatment for protein-losing enteropathy and plastic bronchitis in patients with failing Fontan circulation.

Percutaneous embolization of lymphatic fistulae as treatment for protein-losing enteropathy and plastic bronchitis in patients with failing Fontan circulation.

Journal: Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions

Published: February 01, 2019

Clinical Characteristics of Infective Endocarditis in Children.

Clinical Characteristics of Infective Endocarditis in Children.

Journal: The Pediatric infectious disease journal

Published: October 23, 2018

Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.

Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings.

Journal: PLoS genetics

Published: July 30, 2017

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Journal: American journal of human genetics

Published: March 03, 2016

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Journal: Nature genetics

Published: December 23, 2015

Can a volume challenge pinpoint the limiting factor in a Fontan circulation?

Can a volume challenge pinpoint the limiting factor in a Fontan circulation?

Journal: Acta cardiologica

Published: November 17, 2015

MEIS2 involvement in cardiac development, cleft palate, and intellectual disability.

MEIS2 involvement in cardiac development, cleft palate, and intellectual disability.

Journal: American journal of medical genetics. Part A

Published: November 03, 2014

The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.

The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.

Journal: American journal of medical genetics. Part A

Published: October 09, 2014

Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings.

Homozygous loss-of-function mutation in ALMS1 causes the lethal disorder mitogenic cardiomyopathy in two siblings.

Journal: European journal of medical genetics

Published: February 22, 2014

Use of covered Cheatham-Platinum stents in congenital heart disease.

Use of covered Cheatham-Platinum stents in congenital heart disease.

Journal: International journal of cardiology

Published: November 27, 2013

Showing 1-12 of 16

Last Updated: 09/26/2026