Helle Petri
Copenhagen, Denmark
Last Updated: 09/26/2026
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Found 14 publications
Natural history of cardiac involvement in myotonic dystrophy type 1 - Emphasis on the need for lifelong follow-up.
Journal: International journal of cardiology
Published: May 17, 2023
Congenital myopathies are mainly associated with a mild cardiac phenotype.
Journal: Journal of neurology
Published: November 09, 2018
Echocardiographic and clinical findings in patients with Fabry disease during long-term enzyme replacement therapy: a nationwide Danish cohort study.
Journal: Scandinavian cardiovascular journal : SCJ
Published: May 27, 2017
Frequency and Phenotype of Myotubular Myopathy Amongst Danish Patients with Congenital Myopathy Older than 5 Years.
Journal: Journal of neuromuscular diseases
Published: June 04, 2015
Progression of cardiac involvement in patients with limb-girdle type 2 and Becker muscular dystrophies: a 9-year follow-up study.
Journal: International journal of cardiology
Published: October 09, 2014
Cardiac involvement in myotonic dystrophy: a nationwide cohort study.
Journal: European heart journal
Published: April 19, 2014
Myocardial fibrosis in patients with myotonic dystrophy type 1: a cardiovascular magnetic resonance study.
Journal: Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
Published: April 02, 2014
Ocular, bulbar, limb, and cardiopulmonary involvement in oculopharyngeal muscular dystrophy.
Journal: Acta neurologica Scandinavica
Published: February 07, 2014
High prevalence of cardiac involvement in patients with myotonic dystrophy type 1: a cross-sectional study.
Journal: International journal of cardiology
Published: October 29, 2013
Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: September 24, 2013
Frequency and phenotype of patients carrying TPM2 and TPM3 gene mutations in a cohort of 94 patients with congenital myopathy.
Journal: Neuromuscular disorders : NMD
Published: September 21, 2013
Anoctamin 5 muscular dystrophy in Denmark: prevalence, genotypes, phenotypes, cardiac findings, and muscle protein expression.
Journal: Journal of neurology
Published: March 13, 2013
Last Updated: 09/26/2026