Dario Melgari

San Donato Milanese, Italy

Last Updated: 09/26/2026

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Found 22 publications

Exploring light chain cardiotoxicity in AL amyloidosis: impact on hiPSC-derived cardiomyocyte activity.

Exploring light chain cardiotoxicity in AL amyloidosis: impact on hiPSC-derived cardiomyocyte activity.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: June 19, 2026

Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotonia.

Integrated electrophysiological, cellular, and pharmacological profiling reveals variant-specific mechanisms in SCN4A-related myotonia.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: January 07, 2026

Functional reassessment of Nav1.5 T559A reveals loss-of-function in a variant commonly used as wild type.

Functional reassessment of Nav1.5 T559A reveals loss-of-function in a variant commonly used as wild type.

Journal: American journal of physiology. Cell physiology

Published: July 11, 2025

NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implications.

NaV1.5 autoantibodies in Brugada syndrome: pathogenetic implications.

Journal: European heart journal

Published: December 19, 2023

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights.

Unravelling Novel SCN5A Mutations Linked to Brugada Syndrome: Functional, Structural, and Genetic Insights.

Journal: International journal of molecular sciences

Published: September 08, 2023

A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet.

A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet.

Journal: Epilepsia

Published: July 13, 2023

Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome.

Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome.

Journal: International journal of molecular sciences

Published: February 20, 2023

Alterations of the Sialylation Machinery in Brugada Syndrome.

Alterations of the Sialylation Machinery in Brugada Syndrome.

Journal: International journal of molecular sciences

Published: September 14, 2022

T-Type Calcium Channels: A Mixed Blessing.

T-Type Calcium Channels: A Mixed Blessing.

Journal: International journal of molecular sciences

Published: August 03, 2022

Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly.

Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly.

Journal: Scientific reports

Published: May 01, 2022

Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.

Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.

Journal: International journal of molecular sciences

Published: April 08, 2021

Microtubule polymerization state and clathrin-dependent internalization regulate dynamics of cardiac potassium channel: Microtubule and clathrin control of KV1.5 channel.

Microtubule polymerization state and clathrin-dependent internalization regulate dynamics of cardiac potassium channel: Microtubule and clathrin control of KV1.5 channel.

Journal: Journal of molecular and cellular cardiology

Published: April 14, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026