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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Alessia Gozzini

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JACC. Advances|April 26, 2025

Genotype-Negative Patients With Familial Hypertrophic Cardiomyopathy: Traveling to the "Middle Earth"Francesca Bonanni, Annamaria Del Franco, Valeria Setti, et al.

Journal of Clinical Medicine|April 13, 2023

Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked QuestionsFrancesca Girolami, Alessia Gozzini, Eszter Dalma Pálinkás, et al.

Clinical Epigenetics|July 3, 2021

PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutationsCatia Cavicchi, Abderrahim Oussalah, Silvia Falliano, et al.

European Journal of Human Genetics : EJHG|May 31, 2025

MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patientsMarco Fabiani, Caterina Micolonghi, Silvia Caroselli, et al.

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Search research articles

Showing results (21-30 of 24) with videos related to

Sort By:

Pageof 3

You have reached the last page of results.This site can display upto 24 results.

JACC. Advances|April 26, 2025

Genotype-Negative Patients With Familial Hypertrophic Cardiomyopathy: Traveling to the "Middle Earth"Francesca Bonanni, Annamaria Del Franco, Valeria Setti, et al.

Journal of Clinical Medicine|April 13, 2023

Genetic Testing and Counselling in Hypertrophic Cardiomyopathy: Frequently Asked QuestionsFrancesca Girolami, Alessia Gozzini, Eszter Dalma Pálinkás, et al.

Clinical Epigenetics|July 3, 2021

PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutationsCatia Cavicchi, Abderrahim Oussalah, Silvia Falliano, et al.

European Journal of Human Genetics : EJHG|May 31, 2025

MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patientsMarco Fabiani, Caterina Micolonghi, Silvia Caroselli, et al.

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