Dott. Emanuele Monda

Il dottor Emanuele Monda ha conseguito la laurea in medicina e chirurgia presso l’Università della Campania “Luigi Vanvitelli” e la specializzazione in Malattie dell’Apparato Cardiovascolare presso la medesima Università.

Durante la specializzazione ha svolto la propria attività clinica cardiologica presso l’Ospedale Monaldi di Napoli, dove tuttora lavora, e un periodo di formazione estera presso l’University College London di Londra (UK) dove ha maturato esperienza nella gestione dei pazienti affetti da patologie cardiache dell’adulto e del bambino.

Il suo obiettivo è quello di seguire il paziente durante l’intero percorso diagnostico-terapeutico allo scopo di prevenire e trattare le patologie cardiache e le complicanze ad esse associate.

• Cardiologia
• Cardiologia Pediatrica

• Laura in Medicina e Chirurgia con votazione 110/110 e lode presso Università degli Studi della Campania Luigi Vanvitelli - Napoli, Italia
• Specializzazione in Malattie dell Apparato Cardiovascolare con votazione 50/50 e lode presso Università degli Studi della Campania Luigi Vanvitelli - Napoli, Italia
• Accademico Affiliato presso University College London - Londra, Regno Unito

• Inglese

• Premio Miglior Abstract Presentato al 81° Congresso Nazionale della Società Italiana di Cardiologia (Roma - 2020)
• Premio Miglior Lavoro Pubblicato nel 2021 al 51° Congresso Nazionale della Società Italiana di Cardiologia Pediatrica (Verona - 2022)
• Premio Miglior Abstract al Congresso Cardiomyopathy Mindset - The Bologna Legacy (Bologna - 2023)

• Moscatelli F, Valenzano A, Monda V, Ruberto M, Monda G, Triggiani AI, Monda E, Chieffi S, Villano I, Parisi L, Roccella M, Messina A. Transcranial magnetic stimulation (TMS) application in sport medicine: A brief review. ACTA MEDICA MEDITERR. 2017; 33(3); 423-430. doi: 6384_2017_3_062.
• Messina A, Monda V, Avola R, Moscatelli F, Valenzano AA, Villano I, Ruberto M, Monda E, La Marra M, Tafuri D, Chieffi S, Cibelli G, Monda M, Messina, G. Role of the orexin system on arousal, attention, feeding behaviour and sleep disorders. ACTA MEDICA MEDITERR. 2017; 33(4); 645-649. doi: 6384_2017_4_096.
• Monda V, Nigro E, Ruberto M, Monda G, Valenzano A, Triggiani AI, Moscatelli F, Monda E, Villano I, Roccella M, Parisi L, Messina A. Synergism or competition between zinc and chromium dietary levels on insulin action mechanism. A method to investigate. ACTA MEDICA MEDITERR. 2017; 33(4); 581-585. doi: 6384_2017_4_085.
• Sperandeo R, Maldonato MN, Messina A, Cozzolino P, Monda M, Cerroni F, Romano P, Salerno M, Maltese A, Roccella M, Parisi L, Tripi G, Moscatelli F, Sessa F, Salerno M, Cibelli G, Messina G, Monda V, Chieffi S, Villano I, Monda E, Ruberto M, Marsala G, Marotta R, Valenzano A. Orexin system: Network multi-tasking. ACTA MEDICA MEDITERR. 2018; 34(2); 349-356. doi: 6384_2018_2_55.
• Limongelli G, Monda E, Capozzi G, Caiazza M, Russo MG. Ranolazine treatment for refractory angina in a patient with Hutchinson-Gilford progeria syndrome and end stage aortic stenosis. Cardiogenetics. 2019;9:8609. doi: https://doi.org/10.4081/cardiogenetics.2019.8609.
• Gragnano F, Spedicato V, Frigoli E, Gargiulo G, Di Maio D, Fimiani F, Fioretti V, Annoiato C, Cimmino M, Esposito F, Chianese S, Scalise M, Fimiani L, Franzese M, Monda E, Schiavo A, Cesaro A, De Michele A, Scalise R, Caracciolo A, Andò G, Stabile E, Windecker S, Calabrò P, Valgimigli M. ECG analysis in patients with acute coronary syndrome undergoing invasive management: rationale and design of the electrocardiography sub-study of the MATRIX trial. J Electrocardiol. 2019 Nov-Dec;57:44-54. doi: 10.1016/j.jelectrocard .
• Limongelli G, Monda E, Tramonte S, Gragnano F, Masarone D, Frisso G, Esposito A, Gravino R, Ammendola E, Salerno G, Rubino M, Caiazza M, Russo M, Calabrò P, Elliott PM, Pacileo G. Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy. Int J Cardiol. 2020 Jan 15;299:186-191. doi: 10.1016/j.ijcard .
• Cesaro A, Bianconi V, Gragnano F, Moscarella E, Fimiani F, Monda E, Scudiero O, Limongelli G, Pirro M, Calabrò P. Beyond cholesterol metabolism: The pleiotropic effects of proprotein convertase subtilisin/kexin type 9 (PCSK9). Genetics, mutations, expression, and perspective for long-term inhibition. Biofactors. 2020 May;46(3):367-380. doi: 10.1002/biof.1619.
• Monda E, Fusco A, Melis D, Caiazza M, Gragnano F, Mauriello A, Cirillo A, Rubino M, Esposito A, Grammegna A, Nistri S, Pepe G, Calabrò P, Strisciuglio P, Della Corte A, Oppido G, Russo M, Limongelli G. Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome. Cardiol Young. 2020 May;30(5):663-667. doi: 10.1017/ .
• Limongelli G, Nunziato M, Mazzaccara C, Intrieri M, DArgenio V, Esposito MV, Monda E, Maggio FD, Frisso G, Salvatore F. Genotype-Phenotype Correlation: A Triple DNA Mutational Event in a Boy Entering Sport Conveys an Additional Pathogenicity Risk. Genes (Basel). 2020 May 8;11(5):524. doi: 10.3390/genes11050524.
• Belfiore MP, Iacobellis F, Acampora E, Caiazza M, Rubino M, Monda E, Magaldi MR, Tarallo A, Sasso M, De Pasquale V, Grassi R, Cappabianca S, Calabrò P, Fecarotta S, Esposito S, Esposito G, Pisani A, Pavone LM, Parenti G, Limongelli G. Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases. PLoS One. 2020 May 19;15(5):e0233050. doi: 10.1371/journal.pone.0233050.
• Lombardo B, D'Argenio V, Monda E, Vitale A, Caiazza M, Sacchetti L, Pastore L, Limongelli G, Frisso G, Mazzaccara C. Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome. Mol Genet Genomic Med. 2020 Jul;8(7):e1260. doi: 10.1002/mgg3.1260.
• Monda E, Sarubbi B, Russo MG, Caiazza M, Mazzaccara C, Magrelli J, Rubino M, Esposito A, Perna A, Passariello A, Bossone E, Romeo E, Colonna D, Esposito MV, D'Argenio V, Salvatore F, Pacileo G, Crotti L, Frisso G, Limongelli G. Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivors. Eur J Prev Cardiol. 2020 Jul 26: . doi: 10.1177 .
• Cesaro A, Taglialatela V, Gragnano F, Moscarella E, Fimiani F, Conte M, Barletta V, Monda E, Limongelli G, Severino S, Cirillo P, Calabrò P. Low-Dose Ticagrelor in Patients With High Ischemic Risk and Previous Myocardial Infarction: A Multicenter Prospective Real-World Observational Study. J Cardiovasc Pharmacol. 2020 Aug;76(2):173-180. doi: 10.1097/FJC.0000000000000856.
• Caiazza M, Rubino M, Monda E, Passariello A, Fusco A, Cirillo A, Esposito A, Pierno A, De Fazio F, Pacileo R, Evangelista E, Pacileo G, Russo MG, Limongelli G. Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy. Genes (Basel). 2020 Aug 17;11(8):947. doi: 10.3390/genes11080947.
• Monda E, Palmiero G, Rubino M, Verrillo F, Amodio F, Di Fraia F, Pacileo R, Fimiani F, Esposito A, Cirillo A, Fusco A, Moscarella E, Frisso G, Russo MG, Pacileo G, Calabrò P, Scudiero O, Caiazza M, Limongelli G. Molecular Basis of Inflammation in the Pathogenesis of Cardiomyopathies. Int J Mol Sci. 2020 Sep 4;21(18):6462. doi: 10.3390/ijms21186462.
• Barretta F, Mirra B, Monda E, Caiazza M, Lombardo B, Tinto N, Scudiero O, Frisso G, Mazzaccara C. The Hidden Fragility in the Heart of the Athletes: A Review of Genetic Biomarkers. Int J Mol Sci. 2020 Sep 12;21(18):6682. doi: 10.3390/ijms21186682.
• Esposito A*, Monda E*, Gragnano F, Simone F, Cesaro A, Natale F, Concilio C, Moscarella E, Caiazza M, Pazzanese V, Verrengia M, Valente F, Masarone D, Pelliccia F, Bossone E, Calabro' P, Pacileo G, Limongelli G. Prevalence and clinical implications of hyperhomocysteinaemia in patients with hypertrophic cardiomyopathy and MTHFR C6777T polymorphism. Eur J Prev Cardiol. 2020 Nov;27(17):1906-1908. doi: 10.1177 . *equally contributed
• Monda E, Limongelli G. The hospitalizations in hypertrophic cardiomyopathy: "The dark side of the moon". Int J Cardiol. 2020 Nov 1;318:101-102. doi: 10.1016/j.ijcard .
• Cattadori G, Di Marco S, Farina S, Limongelli G, Monda E, Badagliacca R, Papa S, Tricarico L, Correale M. Beta-blockers in heart failure prognosis: Lessons learned by MECKI Score Group papers. Eur J Prev Cardiol. 2020 Dec;27(2_suppl):65-71. doi: 10.1177 .
• Leonardi S, Gragnano F, Carrara G, Gargiulo G, Frigoli E, Vranckx P, Di Maio D, Spedicato V, Monda E, Fimiani L, Fioretti V, Esposito F, Avvedimento M, Magliulo F, Leone A, Chianese S, Franzese M, Scalise M, Schiavo A, Mazzone P, Esposito G, Andò G, Calabrò P, Windecker S, Valgimigli M. Prognostic Implications of Declining Hemoglobin Content in Patients Hospitalized With Acute Coronary Syndromes. J Am Coll Cardiol. 2021 Feb 2;77(4):375-388. doi: 10.1016/j.jacc .
• Gragnano F, Branca M, Frigoli E, Leonardi S, Vranckx P, Di Maio D, Monda E, Fimiani L, Fioretti V, Chianese S, Esposito F, Franzese M, Scalise M, D'Angelo C, Scalise R, De Blasi G, Andò G, Esposito G, Calabrò P, Windecker S, Pedrazzini G, Valgimigli M; MATRIX Trial Investigators. Access-Site Crossover in Patients With Acute Coronary Syndrome Undergoing Invasive Management. JACC Cardiovasc Interv. 2021 Feb 22;14(4):361-373. doi: 10.1016/j.jcin .
• Monda E, Rubino M, Lioncino M, Di Fraia F, Pacileo R, Verrillo F, Cirillo A, Caiazza M, Fusco A, Esposito A, Fimiani F, Palmiero G, Pacileo G, Calabrò P, Russo MG, Limongelli G. Hypertrophic Cardiomyopathy in Children: Pathophysiology, Diagnosis, and Treatment of Non-sarcomeric Causes. Front Pediatr. 2021 Feb 25;9:632293. doi: 10.3389/fped .
• Cesaro A, Schiavo A, Moscarella E, Coletta S, Conte M, Gragnano F, Fimiani F, Monda E, Caiazza M, Limongelli G, D'Erasmo L, Riccio C, Arca M, Calabrò P. Lipoprotein(a): a genetic marker for cardiovascular disease and target for emerging therapies. J Cardiovasc Med (Hagerstown). 2021 Mar 1;22(3):151-161. doi: 10.2459/JCM.0000000000001077.
• Limongelli G*, Monda E*, D'Aponte A, Caiazza M, Rubino M, Esposito A, Palmiero G, Moscarella E, Messina G, Calabro' P, Scudiero O, Pacileo G, Monda M, Bossone E, Day SM, Olivotto I. Combined Effect of Mediterranean Diet and Aerobic Exercise on Weight Loss and Clinical Status in Obese Symptomatic Patients with Hypertrophic Cardiomyopathy. Heart Fail Clin. 2021 Apr;17(2):303-313. doi: 10.1016/j.hfc . *equally contributed
• Vergara A, Monda E, Mautone C, Renon F, Di Masi A, Giordano M, Limongelli G, Calabrò P, Capozzi G, Russo MG. Rare case of Kawasaki disease with cardiac tamponade and giant coronary artery aneurysms. Cardiol Young. 2021 May;31(5):865-866. doi: 10.1017/ .
• Caiazza M, Lioncino M, Monda E, Di Fraia F, Verrillo F, Pacileo R, Amodio F, Rubino M, Cirillo A, Fusco A, Romeo E, Scatteia A, Dellegrottaglie S, Calabrò P, Sarubbi B, Baban A, Frisso G, Russo MG, Limongelli G. Troponin T Mutation as a Cause of Left Ventricular Systolic Dysfunction in a Young Patient with Previous Surgical Correction of Aortic Coarctation. Biomolecules. 2021 May 6;11(5):696. doi: 10.3390/biom11050696.
• Monda E, Kaski JP, Limongelli G. Editorial: Paediatric Cardiomyopathies. Front Pediatr. 2021 May 11;9:696443. doi: 10.3389/fped .
• Limongelli G, Iucolano S, Monda E, Elefante P, De Stasio C, Lubrano I, Caiazza M, Mazzella M, Fimiani F, Galdo M, De Marchi G, Esposito M, Rubino M, Cirillo A, Fusco A, Esposito A, Trama U, Esposito S, Scarano G, Sepe J, Andria G, Orlando V, Menditto E, Chiodini P; Campania Rare Disease, Iolascon A, Franzese A, Sanduzzi Zamparelli A, Tessitore A, Romano A, Venosa A, Nunzia Olivieri A, Bianco A, La Manna A, Cerbone AM, Spasiano A, Agnese Stanziola A, Colao A, De Bellis A, Gambale A, Toriello A, Tufano A, Ciampa A, Maria Risitano A, Pisani A, Russo A, Volpe A, De Martino B, Amato B, De Fusco C, Piscopo C, Selleri C, Tucci C, Pignata C, Cioffi D, Melis D, Pasquali D, De Brasi D, Spitaleri D, De Brasi D, Russo D, Martellotta D, De Michele E, Varricchio E, Miraglia Del Giudice E, Coscioni E, Cimino E, Pane F, Tranfa F, Pollio F, Lonardo F, Nuzzi F, Simonelli F, Trojsi F, Habetswallner F, Valentini G, Cerbone G, Parenti G, Tedeschi G, Capasso G, Battista Rossi G, Gaglione G, Sarnelli G, Argenziano G, Bellastella G, De Michele G, Fiorentino G, Spadaro G, Scala I, Santoro L, Zeppa L, Auricchio L, Elio Adinolfi L, Alessio M, Amitrano M, Savanelli MC, Russo MG, Ferrucci MG, Carbone MT, Pellecchia MT, Salerno M, Melone M, Del Donno M, Vitale M, Triggiani M, Della Monica M, Lo Presti M, Tenuta M, Mignogna MD, Schiavulli M, Zacchia M, Brunetti-Pierri N, Iovino P, Moscato P, Iandoli R, Scarpa R, Russo R, Troisi S, Sbordone S, Perrotta S, Fecarotta S, Sampaolo S, Cicalese V. Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry. J Public Health (Oxf). 2021 May 13:fdab137. doi: 10.1093/pubmed/fdab137.
• Monda E, Fusco A, Della Corte A, Caiazza M, Cirillo A, Gragnano F, Giugliano MP, Citro R, Rubino M, Esposito A, Cesaro A, Di Fraia F, Palmiero G, Di Maio M, Monda M, Calabrò P, Frisso G, Nistri S; Bicuspid Aortic Valve Consortium (BAVCon), Bossone E, Body SC, Russo MG, Limongelli G. Impact of Regular Physical Activity on Aortic Diameter Progression in Paediatric Patients with Bicuspid Aortic Valve. Pediatr Cardiol. 2021 Jun;42(5):1133-1140. doi: .
• Monda E, Frisso G, Rubino M, Caiazza M, Esposito A, Cirillo A, Fusco A, Palmiero G, Mazzaccara C, Pacileo R, Verrillo F, Di Fraia F, Gragnano F, Cesaro A, Salvatore F, Russo MG, Calabrò P, Pacileo G, Dellegrottaglie S, Limongelli G. Potential role of imaging markers in predicting future disease expression of arrhythmogenic cardiomyopathy. Future Cardiol. 2021 Jul;17(4):647-654. doi: 10.2217/fca-2020-0107.
• Palmiero G, Rubino M, Monda E, Caiazza M, D'Urso L, Carlomagno G, Verrillo F, Ascione R, Manganelli F, Cerciello G, De Rimini ML, Bossone E, Pacileo G, Calabrò P, Golino P, Ascione L, Caso P, Limongelli G. Global Left Ventricular Myocardial Work Efficiency in Heart Failure Patients with Cardiac Amyloidosis: Pathophysiological Implications and Role in Differential Diagnosis. J Cardiovasc Echogr. 2021 Jul-Sep;31(3):157-164. doi: 10.4103/jcecho.jcecho_16_21.
• Limongelli G, Nunziato M, D'Argenio V, Esposito MV, Monda E, Mazzaccara C, Caiazza M, D'Aponte A, D'Andrea A, Bossone E, Maggio FD, Buono P, Pica PW, Capua L, Penco M, Romano S, Paolo FD, Pelliccia A, Frisso G, Salvatore F. Yield and clinical significance of genetic screening in elite and amateur athletes. Eur J Prev Cardiol. 2021 Aug 23;28(10):1081-1090. doi: 10.1177 .
• Monda E, Palmiero G, Lioncino M, Rubino M, Caiazza M, Dongiglio F, Limongelli G. External validation of the increased wall thickness score for the diagnosis of cardiac amyloidosis. Int J Cardiol. 2021 Sep 15;339:99-101. doi: 10.1016/j.ijcard .
• Monda E, Lioncino M, Pacileo R, Rubino M, Cirillo A, Fusco A, Esposito A, Verrillo F, Di Fraia F, Mauriello A, Tessitore V, Caiazza M, Cesaro A, Calabrò P, Russo MG, Limongelli G. Advanced Heart Failure in Special Population-Pediatric Age. Heart Fail Clin. 2021 Oct;17(4):673-683. doi: 10.1016/j.hfc .
• Brancaccio M, Mennitti C, Cesaro A, Monda E, D'Argenio V, Casaburi G, Mazzaccara C, Ranieri A, Fimiani F, Barretta F, Uomo F, Caiazza M, Lioncino M, D'Alicandro G, Limongelli G, Calabrò P, Terracciano D, Lombardo B, Frisso G, Scudiero O. Multidisciplinary In-Depth Investigation in a Young Athlete Suffering from Syncope Caused by Myocardial Bridge. Diagnostics (Basel). 2021 Nov 19;11(11):2144. doi: 10.3390/diagnostics11112144.
• Monda E, Palmiero G, Limongelli G. Left ventricular rotational mechanics in cardiac amyloidosis - reply. Int J Cardiol. 2021 Dec 15;345:152. doi: 10.1016/j.ijcard .
• Gragnano F, Jolly SS, Mehta SR, Branca M, van Klaveren D, Frigoli E, Gargiulo G, Leonardi S, Vranckx P, Di Maio D, Monda E, Fimiani L, Fioretti V, Chianese S, Andò G, Esposito G, Sangiorgi GM, Biondi-Zoccai G, Heg D, Calabrò P, Windecker S, Romagnoli E, Valgimigli M. Prediction of radial crossover in acute coronary syndromes: derivation and validation of the MATRIX score. EuroIntervention. 2021 Dec 17;17(12):1971-1980. doi: 10.4244/11J-D-21-00441.
• Vriz O, AlSergani H, Elshaer AN, Shaik A, Mushtaq AH, Lioncino M, Alamro B, Monda E, Caiazza M, Mauro C, Bossone E, Al-Hassnan ZN, Albert-Brotons D, Limongelli G. A complex unit for a complex disease: the HCM-Family Unit. Monaldi Arch Chest Dis. 2021 Dec 29;92(3). doi: 10.4081/monaldi.2021.2147.
• Monda E, Lioncino M, Rubino M, Caiazza M, Cirillo A, Fusco A, Pacileo R, Fimiani F, Amodio F, Borrelli N, Colonna D, D'Onofrio B, Frisso G, Drago F, Castelletti S, Sarubbi B, Calabrò P, Russo MG, Limongelli G. The Risk of Sudden Unexpected Cardiac Death in Children: Epidemiology, Clinical Causes, and Prevention. Heart Fail Clin. 2022 Jan;18(1):115-123. doi: 10.1016/j.hfc .
• Cirillo A, Lioncino M, Maratea A, Passariello A, Fusco A, Fratta F, Monda E, Caiazza M, Signore G, Esposito A, Baban A, Versacci P, Putotto C, Marino B, Pignata C, Cirillo E, Giardino G, Sarubbi B, Limongelli G, Russo MG. Clinical Manifestations of 22q11.2 Deletion Syndrome. Heart Fail Clin. 2022 Jan;18(1):155-164. doi: 10.1016/j.hfc .
• Fusco A, Mauriello A, Lioncino M, Palmiero G, Fratta F, Granato C, Cirillo A, Caiazza M, Monda E, Credendino A, Signore G, Natale F, Chiosi F, Scarano G, Della Corte A, Nistri S, Russo MG, Limongelli G, Pepe G. The Heart Muscle and Valve Involvement in Marfan Syndrome, Loeys-Dietz Syndromes, and Collagenopathies. Heart Fail Clin. 2022 Jan;18(1):165-175. doi: 10.1016/j.hfc .
• Lioncino M, Monda E, Verrillo F, Moscarella E, Calcagni G, Drago F, Marino B, Digilio MC, Putotto C, Calabrò P, Russo MG, Roberts AE, Gelb BD, Tartaglia M, Limongelli G. Hypertrophic Cardiomyopathy in RASopathies: Diagnosis, Clinical Characteristics, Prognostic Implications, and Management. Heart Fail Clin. 2022 Jan;18(1):19-29. doi: 10.1016/j.hfc .
• Monda E, Lioncino M, Rubino M, Passantino S, Verrillo F, Caiazza M, Cirillo A, Fusco A, Di Fraia F, Fimiani F, Amodio F, Borrelli N, Mauriello A, Natale F, Scarano G, Girolami F, Favilli S, Limongelli G. Diagnosis and Management of Cardiovascular Involvement in Friedreich Ataxia. Heart Fail Clin. 2022 Jan;18(1):31-37. doi: 10.1016/j.hfc .
• Rubino M*, Monda E*, Lioncino M, Caiazza M, Palmiero G, Dongiglio F, Fusco A, Cirillo A, Cesaro A, Capodicasa L, Mazzella M, Chiosi F, Orabona P, Bossone E, Calabrò P, Pisani A, Germain DP, Biagini E, Pieroni M, Limongelli G. Diagnosis and Management of Cardiovascular Involvement in Fabry Disease. Heart Fail Clin. 2022 Jan;18(1):39-49. doi: 10.1016/j.hfc . *equally contributed
• Lioncino M, Monda E, Caiazza M, Fusco A, Cirillo A, Dongiglio F, Simonelli V, Sampaolo S, Ruggiero L, Scarano G, Pota V, Frisso G, Mazzaccara C, D'Amati G, Nigro G, Russo MG, Wahbi K, Limongelli G. Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options. Heart Fail Clin. 2022 Jan;18(1):51-60. doi: 10.1016/j.hfc .
• Palmiero G, Vetrano E, Rubino M, Monda E, Dongiglio F, Lioncino M, Di Fraia F, Caiazza M, Verrillo F, Capodicasa L, Cerciello G, Manganelli F, Catalano M, D'Arienzo D, De Rimini ML, Ascione R, Golino P, Caso P, Ascione L, Limongelli G. The Role of New Imaging Technologies in the Diagnosis of Cardiac Amyloidosis. Heart Fail Clin. 2022 Jan;18(1):61-72. doi: 10.1016/j.hfc .
• Lioncino M, Monda E, Palmiero G, Caiazza M, Vetrano E, Rubino M, Esposito A, Salerno G, Dongiglio F, D'Onofrio B, Verrillo F, Cerciello G, Manganelli F, Pacileo G, Bossone E, Golino P, Calabrò P, Limongelli G. Cardiovascular Involvement in Transthyretin Cardiac Amyloidosis. Heart Fail Clin. 2022 Jan;18(1):73-87. doi: 10.1016/j.hfc .
• Limongelli G, Monda E, Lioncino M, Bossone E. Rare Cardiovascular Diseases: From Genetics to Personalized Medicine. Heart Fail Clin. 2022 Jan;18(1):xix-xxi. doi: 10.1016/j.hfc .
• Rubino M*, Monda E*, Caiazza M, Palmiero G, Lioncino M, Cirillo A, Fusco A, Verrillo F, Perna A, Diana G, Amodio F, Cesaro A, Duro G, Sarubbi B, Russo MG, Calabrò P, Limongelli G. Diagnosis of Fabry Disease in a Patient with a Surgically Repaired Congenital Heart Defect: When Clinical History and Genetics Make the Difference. Cardiogenetics. 2022; 12(1):102-108. https://doi.org/10.3390/card11g1n1t1c112010010. *These authors equally contributed.
• Monda E, Blasi E, De Pasquale A, Di Vilio A, Amodio F, Caiazza M, Diana G, Lioncino M, Perna A, Verrillo F, Martucci ML, Munciguerra O, Vergara A, Limongelli G. Clinical and Molecular Characteristics of Patients with PLN R14del Cardiomyopathy: State-of-the-Art Review. Cardiogenetics. 2022; 12(1):112-121. https://doi.org/10.3390/card11g1n1t1c112010012
• Lioncino M*, Monda E*, Dellegrottaglie S, Cirillo A, Caiazza M, Fusco A, Esposito F, Verrillo F, Ciccarelli G, Rubino M, Triggiani M, Scarpa R, Caforio ALP, Marcolongo R, Rizzo S, Basso C, Nigro G, Russo MG, Golino P, Limongelli G. Pancarditis as the Clinical Presentation of Eosinophilic Granulomatosis with Polyangiitis: A Multimodality Approach to Diagnosis. Cardiogenetics. 2022; 12(2):133-141. https://doi.org/10.3390/card11g1n1t1c112020014. *equally contributed.
• Dongiglio F, Palmiero G, Monda E, Rubino M, Verrillo F, Caiazza M, Cirillo A, Fusco A, Vetrano E, Lioncino M, Diana G, Di Fraia F, Cerciello G, Manganelli F, Vriz O, Limongelli G. Modified Body Mass Index as a Novel Nutritional and Prognostic Marker in Patients with Cardiac Amyloidosis. Cardiogenetics. 2022; 12(2):185-197. https://doi.org/10.3390/card11g1n1t1c112020017.
• Monda E, Palmiero G, Lioncino M, Rubino M, Cirillo A, Fusco A, Caiazza M, Verrillo F, Diana G, Mauriello A, Iavarone M, Losi MA, De Rimini ML, Dellegrottaglie S, D'Andrea A, Bossone E, Pacileo G, Limongelli G. Multimodality Imaging in Cardiomyopathies with Hypertrophic Phenotypes. J Clin Med. 2022 Feb 7;11(3):868. doi: 10.3390/jcm11030868.
• Limongelli G, Monda E, Nunziato M, Salvatore F. Genetic evaluation in athletes and cascade family screening: reply. Eur J Prev Cardiol. 2022 Feb 19;29(1):e41-e43. doi: 10.1093/eurjpc/zwaa150.
• Monda E, Verrillo F, Altobelli I, Lioncino M, Caiazza M, Rubino M, Cirillo A, Fusco A, Esposito A, Di Fraia F, Pacileo R, Gragnano F, Passariello A, Calabrò P, Russo MG, Limongelli G. Natural history of left ventricular hypertrophy in infants of diabetic mothers. Int J Cardiol. 2022 Mar 1;350:77-82. doi: 10.1016/j.ijcard .
• Monda E, Lioncino M, Palmiero G, Franco F, Rubino M, Cirillo A, Verrillo F, Fusco A, Caiazza M, Mazzella M, Moscarella E, Dongiglio F, Sepe J, Pacileo G, Calabrò P, Limongelli G. Bisoprolol for treatment of symptomatic patients with obstructive hypertrophic cardiomyopathy. The BASIC (bisoprolol AS therapy in hypertrophic cardiomyopathy) study. Int J Cardiol. 2022 May 1;354:22-28. doi: 10.1016/j.ijcard .
• Limongelli G, Monda E. Implantable cardioverter defibrillator in hypertrophic cardiomyopathy: Time to avoid unnecessary procedure. Int J Cardiol. 2022 May 15;355:30-31. doi: 10.1016/j.ijcard .
• Monda E, Verrillo F, Rubino M, Palmiero G, Fusco A, Cirillo A, Caiazza M, Guarnaccia N, Mauriello A, Lioncino M, Perna A, Diana G, D'Andrea A, Bossone E, Calabrò P, Limongelli G. Thoracic Aortic Dilation: Implications for Physical Activity and Sport Participation. Diagnostics (Basel). 2022 Jun 4;12(6):1392. doi: 10.3390/diagnostics12061392.
• Limongelli G, Adorisio R, Baggio C, Bauce B, Biagini E, Castelletti S, Favilli S, Imazio M, Lioncino M, Merlo M, Monda E, Olivotto I, Parisi V, Pelliccia F, Basso C, Sinagra G, Indolfi C, Autore C; WG on Cardiomyopathies of SIC (Società Italiana di Cardiologia); WG on Cardiomyopathies of SICPed (Società Italiana di Cardiologia Pediatrica). Diagnosis and Management of Rare Cardiomyopathies in Adult and Paediatric Patients. A Position Paper of the Italian Society of Cardiology (SIC) and Italian Society of Paediatric Cardiology (SICP). Int J Cardiol. 2022 Jun 15;357:55-71. doi: 10.1016/j.ijcard .
• Girolami F, Iascone M, Pezzoli L, Passantino S, Limongelli G, Monda E, Rubino M, Adorisio R, Lombardi M, Ragni L, Olivotto I, Favilli S; a nome della Società Italiana di Cardiologia Pediatrica (SICP). Indicazioni all’esecuzione del test genetico nella diagnosi delle cardiomiopatie ad esordio pediatrico: percorso clinico della Società Italiana di Cardiologia Pediatrica [Clinical pathway on pediatric cardiomyopathies: a genetic testing strategy proposed by the Italian Society of Pediatric Cardiology]. G Ital Cardiol (Rome). 2022 Jul;23(7):505-515. Italian. doi: 38168.
• Monda E, Limongelli G. A Roadmap to Predict Adverse Outcome in Fabry Disease. J Am Coll Cardiol. 2022 Sep 6;80(10):995-997. doi: 10.1016/j.jacc .
• Iavarone M*, Monda E*, Vritz O, Calila Albert D, Rubino M, Verrillo F, Caiazza M, Lioncino M, Amodio F, Guarnaccia N, Gragnano F, Lombardi R, Esposito G, Bossone E, Calabrò P, Losi MA, Limongelli G. Medical treatment of patients with hypertrophic cardiomyopathy: An overview of current and emerging therapy. Arch Cardiovasc Dis. 2022 Oct;115(10):529-537. doi: 10.1016/j.acvd . *equally contributed
• Lioncino M, Fusco A, Monda E, Colonna D, Sibilio M, Caiazza M, Magri D, Borrelli AC, D'Onofrio B, Mazzella ML, Colantuono R, Arienzo MR, Sarubbi B, Russo MG, Chello G, Limongelli G. Severe Lymphatic Disorder and Multifocal Atrial Tachycardia Treated with Trametinib in a Patient with Noonan Syndrome and SOS1 Mutation. Genes (Basel). 2022 Aug 23;13(9):1503. doi: 10.3390/genes13091503.
• Monda E, Limongelli G. Is There a Role for Genetic Testing in Patients With Myocarditis? Circ Genom Precis Med. 2022 Oct;15(5):e003824. doi: 10.1161/CIRCGEN.122.003824.
• Monda E, Lioncino M, Limongelli G. Sudden cardiac death risk prediction in arrhythmogenic right ventricular cardiomyopathy: the challenge of complex statistical modelling and its impact in clinical practice. Eur Heart J. 2022 Dec 14;43(47):4960. doi: 10.1093/eurheartj/ehac538.
• Mazzaccara C, Lombardi R, Mirra B, Barretta F, Esposito MV, Uomo F, Caiazza M, Monda E, Losi MA, Limongelli G, D'Argenio V, Frisso G. Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes. Biomolecules. 2022 Oct 3;12(10):1417. doi: 10.3390/biom12101417.
• Amodio F, Caiazza M, Monda E, Rubino M, Capodicasa L, Chiosi F, Simonelli V, Dongiglio F, Fimiani F, Pepe N, Chimenti C, Calabrò P, Limongelli G. An Overview of Molecular Mechanisms in Fabry Disease. Biomolecules. 2022 Oct 12;12(10):1460. doi: 10.3390/biom12101460.
• Delogu AB, Limongelli G, Versacci P, Adorisio R, Kaski JP, Blandino R, Maiolo S, Monda E, Putotto C, De Rosa G, Chatfield KC, Gelb BD, Calcagni G. The heart in RASopathies. Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):440-451. doi: 10.1002/ajmg.c.32014.
• Monda E, Caiazza M, Limongelli G. The Expanding Spectrum of FLNC Cardiomyopathy. Cardiogenetics 2022, 12, 276–277. doi: 10.3390/card11g1n1t1c112040027.
• Natale F, Molinari R, Covino S, Piccinocchi G, Salvetti A, Monda E, Limongelli G, Cimmino G. Effectiveness in the short-term of a novel nutraceutical for the management of hypercholesterolemia: an observational multicenter primary care experience in a large population of patients at low to moderate cardiovascular risk. Functional Foods in Health and Disease 2022; 12(11): 627-638. doi: 10.31989/ffhd.v12i11.1023.
• Dongiglio F, Monda E, Palmiero G, Verrillo F, Rubino M, Diana G, Cirillo A, Fusco A, Vetrano E, Lioncino M, Caiazza M, Cerciello G, Capodicasa L, Chiosi F, Simonelli V, De Rimini ML, Natale F, Di Santo A, Moscarella E, Calabrò P, Limongelli G. Pathophysiology, Functional Assessment and Prognostic Implications of Nutritional Disorders in Systemic Amyloidosis. J Clin Med. 2023 Jan 9;12(2):528. doi: 10.3390/jcm12020528.
• Monda E, Limongelli G. Integrated Sudden Cardiac Death Risk Prediction Model For Patients With Hypertrophic Cardiomyopathy. Circulation. 2023 Jan 24;147(4):281-283. doi: 10.1161/CIRCULATIONAHA.122.063019.
• Limongelli G*, Monda E*, Lioncino M, Di Paolo F, Ferrara F, Vriz O, Calabro P, Bossone E, Pelliccia A. Aortic root diameter in highly-trained competitive athletes: reference values according to sport and prevalence of aortic enlargement. Can J Cardiol. 2023 Feb 17:10828-282X(23)00135-6. doi: 10.1016/j.cjca . *equally contributed
• Monda E, Lioncino M, Verrillo F, Rubino M, Caiazza M, Mauriello A, Guarnaccia N, Fusco A, Cirillo A, Covino S, Altobelli I, Diana G, Palmiero G, Dongiglio F, Natale F, Cesaro A, Bossone E, Russo MG, Calabrò P, Limongelli G. The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases. Diagnostics (Basel). 2023 Feb 17;13(4):772. doi: 10.3390/diagnostics13040772.
• Monda E, Rubino M, Palmiero G, Verrillo F, Lioncino M, Diana G, Cirillo A, Fusco A, Dongiglio F, Caiazza M, Altobelli I, Mauriello A, Guarnaccia N, Scatteia A, Cesaro A, Pacileo G, Sarubbi B, Frisso G, Bauce B, D'Andrea A, Dellegrottaglie S, Russo MG, Calabrò P, Limongelli G. Multimodality Imaging in Arrhythmogenic Left Ventricular Cardiomyopathy. J Clin Med. 2023 Feb 16;12(4):1568. doi: 10.3390/jcm12041568.
• Monda E, Kaski JP, Limongelli G. Editorial: Cardiovascular genetics-focus on paediatric cardiomyopathy. Front Pediatr. 2023 Feb 10;11:1147527. doi: 10.3389/fped .
• Monda E, Limongelli G. Heart failure with preserved ejection fraction: the need for a better genetic characterization. Eur Heart J Cardiovasc Imaging. 2023 Apr 24;24(5):e89. doi: 10.1093/ehjci/jead043.
• Andreini D, Bauce B, Limongelli G, Monosilio S, Di Lorenzo F, Angelini F, Melotti E, Monda E, Mango R, Toso E, Maestrini V. Sport activity in patients with cardiomyopathies: a review. J Cardiovasc Med (Hagerstown). 2023 May 1;24(Suppl 2):e116-e127. doi: 10.2459/JCM.0000000000001470.
• Autore C, Bariani R, Bauce B, Biagini E, Canepa M, Castelletti S, Crotti L, Limongelli G, Merlo M, Monda E, Pio Loco Detto Gava C, Parisi V, Tini G, Imazio M. From the phenotype to precision medicine: an update on the cardiomyopathies diagnostic workflow. J Cardiovasc Med (Hagerstown). 2023 May 1;24(Suppl 2):e178-e186. doi: 10.2459/JCM.0000000000001424.
• Monda E, Elliott PM. Personalized Medicine in Sports Cardiology: Managing the Known Unknowns. Eur J Prev Cardiol. 2023 May 17:zwad153. doi: 10.1093/eurjpc/zwad153.
• Lioncino M*, Monda E*, Caiazza M, Simonelli V, Nesti C, Mauriello A, Budillon A, Di Santo A, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies. Circ Genom Precis Med. 2023 May 17:e004122. doi: 10.1161/CIRCGEN.123.004122. *equally contributed
• Monda E, Prosnitz A, Aiello R, Lioncino M, Norrish G, Caiazza M, Drago F, Beattie M, Tartaglia M, Russo MG, Colan SD, Calcagni G, Gelb BD, Kaski JP, Roberts AE, Limongelli G. Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines. Circ Genom Precis Med. 2023 May 18:e003861. doi: 10.1161/CIRCGEN.122.003861.
• Monda E, Lioncino M, Caiazza M, Simonelli V, Nesti C, Rubino M, Perna A, Mauriello A, Budillon A, Pota V, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes. Int J Mol Sci. 2023 May 22;24(10):9108. doi: 10.3390/ijms24109108.
• Monda E, Limongelli G. Thromboembolic events in peripartum cardiomyopathy: Current dilemmas and future perspectives. Eur J Heart Fail. 2023 Jun 16. doi: 10.1002/ejhf.2937.
• Monda E, Limongelli G. Letter by Monda and Limongelli Regarding Article, "The Prevalence and Association of Exercise Test Abnormalities With Sudden Cardiac Death and Transplant-Free Survival in Childhood Hypertrophic Cardiomyopathy". Circulation. 2023 Jul 4;148(1):73. doi: 10.1161/CIRCULATIONAHA.123.064744.
• Palmiero G*, Monda E*, Verrillo F, Dongiglio F, Caiazza M, Rubino M, Lioncino M, Diana G, Vetrano E, Fusco A, Cirillo A, Mauriello A, Ciccarelli G, Ascione L, De Rimini ML, D'Alto M, Cerciello G, D'Andrea A, Golino P, Calabrò P, Bossone E, Limongelli G. Prevalence and clinical significance of right ventricular pulmonary arterial uncoupling in cardiac amyloidosis. Int J Cardiol. 2023 Oct 1;388:131147. doi: 10.1016/j.ijcard . *equally contributed
• Monda E, Bakalakos A, Rubino M, Verrillo F, Diana G, De Michele G, Altobelli I, Lioncino M, Perna A, Falco L, Palmiero G, Elliott PM, Limongelli G. Targeted Therapies in Pediatric and Adult Patients With Hypertrophic Heart Disease: From Molecular Pathophysiology to Personalized Medicine. Circ Heart Fail. 2023 Aug;16(8):e010687. doi: 10.1161/CIRCHEARTFAILURE.123.010687.
• Monda E, Falco L, Palmiero G, Rubino M, Perna A, Diana G, Verrillo F, Dongiglio F, Cirillo A, Fusco A, Caiazza M, Limongelli G. Cardiovascular Involvement in Fabry's Disease: New Advances in Diagnostic Strategies, Outcome Prediction and Management. Card Fail Rev. 2023 Aug 8;9:e12. doi: 10.15420/cfr.2023.06.
• Monda E, Rubino M, Riccio E, Caiazza M, Iaccarino G, Dongiglio F, Graziani F, Pisani A, Limongelli G. Clinical manifestation of patients with Fabry disease and R356W GLA variant. Int J Cardiol. 2023 Aug 22:131295. doi: 10.1016/j.ijcard .
• Vergara A, De Felice M, Cesaro A, Gragnano F, Pariggiano I, Golia E, De Pasquale A, Blasi E, Fimiani F, Monda E, Limongelli G, Calabrò P. Immune-Checkpoint Inhibitor-Related Myocarditis: Where We Are and Where We Will Go. Angiology. 2023 Sep 12: doi: 10.1177/ .
• Caiazza M, Budillon A, Monda E, Aruta G, Esposito A, Del Vecchio Blanco F, Piluso G, Nigro V, Scarano G, Limongelli G. An atypical Aymé-Gripp phenotype detected by exome sequencing. Am J Med Genet A. 2023 Sep 15. doi: 10.1002/ajmg.a.63406.
• Monda E, Limongelli G, Pelliccia F. Hypertrophic Cardiomyopathy-Current Challenges and Future Perspectives. J Clin Med. 2023 Sep 21;12(18):6093. doi: 10.3390/jcm12186093.
• Meucci MC, Lillo R, Del Franco A, Monda E, Iannaccone G, Baldassarre R, Di Nicola F, Parisi V, Lombardo A, Spinelli L, Biagini E, Pieroni M, Pisani A, Crea F, Iaccarino G, Limongelli G, Olivotto I, Graziani F. Prognostic Implications of the Extent of Cardiac Damage in Patients With Fabry Disease. J Am Coll Cardiol. 2023 Oct 10;82(15):1524-1534. doi: 10.1016/j.jacc .

• Dolore toracico
• Palpitazioni
• Cardiopalmo
• Dispnea
• Sincope
• Soffio cardiaco
• Ipertensione
• Dislipidemia
• Ipercolesterolemia
• Scompenso cardiaco
• Insufficienza cardiaca
• Valvulopatie
• Stenosi aortica
• Insufficienza aortica
• Stenosi mitralica
• Insufficienza mitralica
• Cardiopatie congenite
• Forame ovale pervio
• Cardiomiopatie
• Cardiomiopatia ipertrofica
• Cardiomiopatia dilatativa
• Malattie cardiovascolari
• Aritmia
• Fibrillazione atriale
• Morte improvvisa
• Pericardite
• Miocardite