Julie Proukhnitzky

Paris, France

Last Updated: 09/26/2026

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Found 17 publications

Is there an effect of gender on phenotypical expression of genetically mediated sinus node dysfunction?

Is there an effect of gender on phenotypical expression of genetically mediated sinus node dysfunction?

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: April 07, 2026

Sudden cardiac death and major arrhythmic events in patients with Fabry disease: risk stratification in the FHFc multicenter study.

Sudden cardiac death and major arrhythmic events in patients with Fabry disease: risk stratification in the FHFc multicenter study.

Journal: Heart rhythm

Published: January 09, 2026

Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathies.

Family history of sudden cardiac death as a risk marker for ventricular arrhythmias in laminopathies.

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: July 04, 2025

Laminopathies: natural history and risk prediction of heart failure.

Laminopathies: natural history and risk prediction of heart failure.

Journal: European heart journal

Published: June 06, 2025

Modern clinical genetics in cardiology.

Modern clinical genetics in cardiology.

Journal: Heart (British Cardiac Society)

Published: January 11, 2025

A family-based strategy to identify and prevent premature cardiovascular disease: a feasibility pilot study.

A family-based strategy to identify and prevent premature cardiovascular disease: a feasibility pilot study.

Journal: European journal of preventive cardiology

Published: November 22, 2024

Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic Counseling.

Exploring the Familial Phenotypic Variability Associated With TTN Truncating Variants in Cardiomyopathies: Variant Spectrum, Genotype-Phenotype Correlation and Consequences in Genetic Counseling.

Journal: Clinical genetics

Published: October 08, 2024

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Journal: European heart journal

Published: September 18, 2024

Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathies.

Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathies.

Journal: International journal of cardiology

Published: June 25, 2024

Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis.

Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis.

Journal: Orphanet journal of rare diseases

Published: June 10, 2024

Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies.

Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategies.

Journal: Orphanet journal of rare diseases

Published: June 10, 2024

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Systematic analysis of SCN5A variants associated with inherited cardiac diseases.

Journal: Heart rhythm

Published: June 06, 2024

Showing 1-12 of 17

Last Updated: 09/26/2026