Apollonia M. Van Den Enden-Helderman

Maastricht, LI 6229HX, Netherlands

Last Updated: 09/26/2026

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Found 13 publications

Dipeptidyl aminopeptidase-like protein 6 regulates the INa-Ito balance influencing cardiac electrophysiology and arrhythmogenesis.

Dipeptidyl aminopeptidase-like protein 6 regulates the INa-Ito balance influencing cardiac electrophysiology and arrhythmogenesis.

Journal: Science translational medicine

Published: April 29, 2026

Pregnancy and Delivery Outcomes in Vascular Ehlers-Danlos Syndrome: A Retrospective Multicentre Cohort Study.

Pregnancy and Delivery Outcomes in Vascular Ehlers-Danlos Syndrome: A Retrospective Multicentre Cohort Study.

Journal: BJOG : an international journal of obstetrics and gynaecology

Published: December 05, 2024

Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.

Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.

Journal: Circulation. Genomic and precision medicine

Published: April 16, 2024

Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A: sentinel event for evolving dilated cardiomyopathy-a case report.

Juvenile-onset multifocal atrial arrhythmias, atrial standstill and compound heterozygosity of genetic variants in TAF1A: sentinel event for evolving dilated cardiomyopathy-a case report.

Journal: European heart journal. Case reports

Published: November 11, 2022

Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy.

Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy.

Journal: European journal of human genetics : EJHG

Published: October 27, 2022

Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death.

Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death.

Journal: Heart rhythm

Published: June 27, 2022

Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN).

Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN).

Journal: European journal of medical genetics

Published: December 30, 2021

A mutation update for the FLNC gene in myopathies and cardiomyopathies.

A mutation update for the FLNC gene in myopathies and cardiomyopathies.

Journal: Human mutation

Published: December 20, 2019

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

Journal: British journal of cancer

Published: March 07, 2018

Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy.

Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy.

Journal: European journal of human genetics : EJHG

Published: January 12, 2018

Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death.

Heritability in a SCN5A-mutation founder population with increased female susceptibility to non-nocturnal ventricular tachyarrhythmia and sudden cardiac death.

Journal: Heart rhythm

Published: February 10, 2017

Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.

Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.

Journal: European heart journal

Published: April 01, 2015

Showing 1-12 of 13

Last Updated: 09/26/2026