Massimiliano Cecconi
Genoa, Italy
Last Updated: 09/26/2026
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Found 10 publications
Autosomal recessive hypertrophic cardiomyopathy associated with variants in TRIM63.
Journal: International journal of cardiology
Published: September 05, 2025
Desmin c.322G>A variant is associated with cardiomyopathy: a case series.
Journal: Journal of cardiovascular medicine (Hagerstown, Md.)
Published: July 02, 2025
Prevalence of rare missense TTN variants in a cohort of patients with cardiomyopathy.
Journal: Journal of molecular and cellular cardiology
Published: June 19, 2024
Remission of eczema and recovery of Th1 polarization following treatment with Dupilumab in STAT3 hyper IgE syndrome.
Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology
Published: January 19, 2022
qPCR Applications for the Determination of the Biological Age.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: October 04, 2019
Expanding the Clinical Spectrum of Sotos Syndrome in a Patient with the New "c.[5867T>A]+[=]"; "p.[Leu1956Gln]+[=]" NSD1 Missense Mutation and Complex Skin Hamartoma.
Journal: International journal of molecular sciences
Published: September 05, 2018
Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy.
Journal: International journal of molecular medicine
Published: June 01, 2016
Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy.
Journal: The American journal of cardiology
Published: April 01, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026