Valentina Ferradini
Rome, 00133, Italy
Last Updated: 09/26/2026
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Found 18 publications
The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and Channelopathies.
Journal: Journal of cardiovascular development and disease
Published: June 09, 2025
Donor selection for allogeneic hematopoietic cell transplant in a patient with JAK2 V617F primary myelofibrosis and SH2B3/LNK germline variant.
Journal: Annals of hematology
Published: September 12, 2024
Spontaneous coronary artery dissection: review, case report and analysis of COVID-19-related cases.
Journal: Minerva cardiology and angiology
Published: February 27, 2023
DSP-Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort.
Journal: International journal of molecular sciences
Published: January 13, 2023
A likely pathogenic ACTG1 variant in a child showing partial phenotypic overlap with Baraitser-Winter syndrome.
Journal: American journal of medical genetics. Part A
Published: October 05, 2022
Case Report: Crossing a rugged road in a primary immune regulatory disorder.
Journal: Frontiers in pediatrics
Published: September 27, 2022
Clinical Features of LMNA-Related Cardiomyopathy in 18 Patients and Characterization of Two Novel Variants.
Journal: Journal of clinical medicine
Published: September 09, 2021
Genetic and Epigenetic Factors of Takotsubo Syndrome: A Systematic Review.
Journal: International journal of molecular sciences
Published: July 27, 2021
Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 31, 2019
Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.
Journal: Frontiers in immunology
Published: May 08, 2019
Last Updated: 09/26/2026