Mattia Zampieri

Meyer Children's Hospital — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index1.3kcitations110works9.62yr avg
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Research Topics

Amyloidosis: Diagnosis, Treatment, Outcomes(55), Cardiomyopathy and Myosin Studies(40), Parathyroid Disorders and Treatments(34), Cardiovascular Function and Risk Factors(28), Peptidase Inhibition and Analysis(13)

Publications110 total

Mavacamten in the Treatment of Obstructive Hypertrophic Cardiomyopathy: from Pathophysiology To Real World Data
Current Cardiology Reports·2025· 1 citedOpen Access
Autosomal recessive hypertrophic cardiomyopathy associated with variants in TRIM63
International Journal of Cardiology·2025· 1 citedOpen Access
Neurohormonal therapies at baseline and follow-up and survival in wild-type transthyretin cardiac amyloidosis
Journal of Cardiovascular Medicine·2025· 1 citedOpen Access
Hypertrophic cardiomyopathy: changing the paradigm of exercise prescription and competitive sport participation
European Heart Journal·2025· 3 citedOpen Access
Genetic Profile of Pediatric-Onset Cardiac Channelopathies
Cardiogenetics·2025Open Access
Genetic Profile of Pediatric-Onset Cardiac Channelopathies
Preprints.org·2025Open Access
Major arrhythmias in non-dilated left ventricular cardiomyopathy: a novel prediction score
European Heart Journal·2025· 10 cited
Outcome and Disease Progression in NYHA Functional Class I and II Patients With Wild-Type Transthyretin Cardiomyopathy Treated With Tafamidis
JACC Heart Failure·2025· 4 citedOpen Access
Prognostic Value of Malnutrition, Frailty, and Physical Performance in Transthyretin Cardiac Amyloidosis: Insights From a Prospective Multicenter Cohort Study
Circulation Heart Failure·2025· 1 citedOpen Access
Yield of Genetic Testing in Pediatric Cardiomyopathies: Implications for Novel Therapeutic Options
Molecular Genetics & Genomic Medicine·2025· 1 citedOpen Access
The American College of Cardology/American Heart Association Heart Failure Staging System Highlights Diagnostic Delay and Predicts Outcome in Transthyretin Cardiac Amyloidosis
Mayo Clinic Proceedings·2025· 1 citedOpen Access
NEUROHORMONAL THERAPIES AT BASELINE AND FOLLOW–UP AND SURVIVAL IN PATIENTS WITH WILD–TYPE TRANSTHYRETIN CARDIAC AMYLOIDOSIS
European Heart Journal Supplements·2025
Frailty, disability, and malnutrition assessment for preventive measure in transthyretin cardiac amyloidosis
European Journal of Preventive Cardiology·2025Open Access
Clinical Phenotype and Prognostic Significance of Frailty in Transthyretin Cardiac Amyloidosis
JACC CardioOncology·2025· 12 citedOpen Access
Prognostic impact of hypertension and diabetes in patients with cardiac amyloidosis
International Journal of Cardiology·2025· 5 citedOpen Access
Clinical Phenotype and Prognosis of Asymptomatic Patients With Transthyretin Cardiac Amyloid Infiltration
JAMA Cardiology·2025· 26 citedOpen Access
The Issue of Genetic Counselling and Testing in Minors with Cardiomyopathies in a Diagnostic or Predictive Setting: Benefits and Harms
SSRN Electronic Journal·2025Open Access
Echocardiographic assessment of left ventricular hemodynamic forces in hypertrophic cardiomyopathy
European Heart Journal - Cardiovascular Imaging·2025Open Access
Progression and Prognostic Significance of Electrocardiographic Findings in Patients with Cardiac Amyloidosis
ESC Heart Failure·2024· 2 citedOpen Access
Distal His Pacing Promotes Reverse Remodeling in a Child With Conventional Pacing‐Induced Ventricular Dysfunction
Pacing and Clinical Electrophysiology·2024· 1 cited
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Frequent Co-authors

Francesco Cappelli(41), Federico Perfetto(28), Iacopo Olivotto(28), Alessia Argirò(25), Carlo Fumagalli(18), Alessia Tomberli(14), Carlo Di Mario(13), Alberto Marchi(12), Aldostefano Porcari(11), Niccolò Marchionni(11), Beatrice Musumeci(10), Alberto Cipriani(10), Gianfranco Sinagra(10), Giacomo Tini(10), Marco Allinovi(10), Chiara Zocchi(10), Luigi Tassetti(10), Martina Gabriele(9), Simone Longhi(8), Marco Canepa(8)