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BMC Cardiovascular Disorders
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June 17, 2026
Clinical spectrum, cardiac phenotypes, and outcomes of FHL1-related cardiomyopathies: a systematic review
Emanuele Bobbio, Martina Caiazza, Filomena Pisacane, et al.
Archives of Cardiovascular Diseases
|
September 11, 2022
Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy
Michele Iavarone, Emanuele Monda, Olga Vritz, et al.
Circulation. Genomic and Precision Medicine
|
May 17, 2023
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
International Journal of Cardiology
|
May 7, 2024
Effect of beta-blockers and angiotensin receptor blockers in reducing the aortic growth rate in children with bicuspid aortic valve-related aortopathy
Emanuele Monda, Antonella Boccia, Ippolita Altobelli, et al.
Cardiology in the Young
|
April 16, 2020
Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome
Emanuele Monda, Adelaide Fusco, Daniela Melis, et al.
European Journal of Preventive Cardiology
|
November 14, 2019
Prevalence and clinical implications of hyperhomocysteinaemia in patients with hypertrophic cardiomyopathy and MTHFR C6777T polymorphism
Augusto Esposito, Emanuele Monda, Felice Gragnano, et al.
Heart Failure Clinics
|
November 15, 2021
Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
Emanuele Monda, Michele Lioncino, Marta Rubino, et al.
Heart Failure Clinics
|
November 15, 2021
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
Circulation. Genomic and Precision Medicine
|
May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines
Emanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
Scientific Reports
|
November 11, 2025
Argo Delphi consensus statement on red flags and clinical gateways towards rare disease diagnosis
Giuseppe Limongelli, Fabio De Iaco, Marta Mosca, et al.
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Search research articles
Search
Showing results (51-60 of 98) with videos related to
Sort By:
Page
of 10
BMC Cardiovascular Disorders
|
June 17, 2026
Clinical spectrum, cardiac phenotypes, and outcomes of FHL1-related cardiomyopathies: a systematic review
Emanuele Bobbio, Martina Caiazza, Filomena Pisacane, et al.
Archives of Cardiovascular Diseases
|
September 11, 2022
Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy
Michele Iavarone, Emanuele Monda, Olga Vritz, et al.
Circulation. Genomic and Precision Medicine
|
May 17, 2023
Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
International Journal of Cardiology
|
May 7, 2024
Effect of beta-blockers and angiotensin receptor blockers in reducing the aortic growth rate in children with bicuspid aortic valve-related aortopathy
Emanuele Monda, Antonella Boccia, Ippolita Altobelli, et al.
Cardiology in the Young
|
April 16, 2020
Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome
Emanuele Monda, Adelaide Fusco, Daniela Melis, et al.
European Journal of Preventive Cardiology
|
November 14, 2019
Prevalence and clinical implications of hyperhomocysteinaemia in patients with hypertrophic cardiomyopathy and MTHFR C6777T polymorphism
Augusto Esposito, Emanuele Monda, Felice Gragnano, et al.
Heart Failure Clinics
|
November 15, 2021
Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia
Emanuele Monda, Michele Lioncino, Marta Rubino, et al.
Heart Failure Clinics
|
November 15, 2021
Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options
Michele Lioncino, Emanuele Monda, Martina Caiazza, et al.
Circulation. Genomic and Precision Medicine
|
May 18, 2023
Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines
Emanuele Monda, Aaron Prosnitz, Rossella Aiello, et al.
Scientific Reports
|
November 11, 2025
Argo Delphi consensus statement on red flags and clinical gateways towards rare disease diagnosis
Giuseppe Limongelli, Fabio De Iaco, Marta Mosca, et al.
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of 10