Michele Nicastro
Amsterdam, NH, Netherlands
Last Updated: 09/26/2026
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Found 8 publications
Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.
Journal: American journal of human genetics
Published: August 18, 2024
Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.
Journal: medRxiv : the preprint server for health sciences
Published: July 15, 2024
To shift or to rotate? Comparison of acquisition strategies for multi-slice super-resolution magnetic resonance imaging.
Journal: Frontiers in neuroscience
Published: September 14, 2022
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: April 27, 2022
Acetylcholine Reduces IKr and Prolongs Action Potentials in Human Ventricular Cardiomyocytes.
Journal: Biomedicines
Published: December 24, 2021
Model-based super-resolution reconstruction with joint motion estimation for improved quantitative MRI parameter mapping.
Journal: Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society
Published: November 26, 2021
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Journal: Nature genetics
Published: September 25, 2020
Showing 1-8 of 8
Last Updated: 09/26/2026