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112 results

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Page 1
Prevalence and clinical significance of right ventricular pulmonary arterial uncoupling in cardiac amyloidosis.
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. Palmiero G, et al. Among authors: caiazza m. Int J Cardiol. 2023 Oct 1;388:131147. doi: 10.1016/j.ijcard.2023.131147. Epub 2023 Jul 7. Int J Cardiol. 2023. PMID: 37423570
Hereditary hypochromic microcytic anemia associated with loss-of-function DMT1 gene mutations and absence of liver iron overload.
Casale M, Borriello A, Scianguetta S, Roberti D, Caiazza M, Bencivenga D, Tartaglione I, Ladogana S, Maruzzi M, Della Ragione F, Perrotta S. Casale M, et al. Among authors: caiazza m. Am J Hematol. 2018 Mar;93(3):E58-E60. doi: 10.1002/ajh.24988. Epub 2017 Dec 8. Am J Hematol. 2018. PMID: 29178181 Free article. No abstract available.
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia.
Cappellini MD, Viprakasit V, Taher AT, Georgiev P, Kuo KHM, Coates T, Voskaridou E, Liew HK, Pazgal-Kobrowski I, Forni GL, Perrotta S, Khelif A, Lal A, Kattamis A, Vlachaki E, Origa R, Aydinok Y, Bejaoui M, Ho PJ, Chew LP, Bee PC, Lim SM, Lu MY, Tantiworawit A, Ganeva P, Gercheva L, Shah F, Neufeld EJ, Thompson A, Laadem A, Shetty JK, Zou J, Zhang J, Miteva D, Zinger T, Linde PG, Sherman ML, Hermine O, Porter J, Piga A; BELIEVE Investigators. Cappellini MD, et al. N Engl J Med. 2020 Mar 26;382(13):1219-1231. doi: 10.1056/NEJMoa1910182. N Engl J Med. 2020. PMID: 32212518 Clinical Trial.
Severe hypertrophic cardiomyopathy in a patient with atypical Anderson-Fabry disease.
Masarone D, Duro G, Dellegrottaglie S, Colomba P, Rubino M, Cirillo A, Pisani A, Caiazza M, Elliott PM, Calabrò P, Pacileo G, Limongelli G. Masarone D, et al. Among authors: caiazza m. Future Cardiol. 2017 Nov;13(6):521-527. doi: 10.2217/fca-2017-0011. Epub 2017 Sep 22. Future Cardiol. 2017. PMID: 28936893
Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy.
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. Limongelli G, et al. Among authors: caiazza m. Int J Cardiol. 2020 Jan 15;299:186-191. doi: 10.1016/j.ijcard.2019.06.073. Epub 2019 Jul 4. Int J Cardiol. 2020. PMID: 31303393
Prevalence and clinical implications of hyperhomocysteinaemia in patients with hypertrophic cardiomyopathy and MTHFR C6777T polymorphism.
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. Esposito A, et al. Among authors: caiazza m. Eur J Prev Cardiol. 2020 Nov;27(17):1906-1908. doi: 10.1177/2047487319888596. Epub 2019 Nov 12. Eur J Prev Cardiol. 2020. PMID: 31718272 No abstract available.
Clinical significance of family history and bicuspid aortic valve in children and young adult patients with Marfan syndrome.
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. Monda E, et al. Among authors: caiazza m. Cardiol Young. 2020 May;30(5):663-667. doi: 10.1017/S1047951120000748. Epub 2020 Apr 15. Cardiol Young. 2020. PMID: 32290873
Aortopathies in mouse models of Pompe, Fabry and Mucopolysaccharidosis IIIB lysosomal storage diseases.
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. Belfiore MP, et al. Among authors: caiazza m. PLoS One. 2020 May 19;15(5):e0233050. doi: 10.1371/journal.pone.0233050. eCollection 2020. PLoS One. 2020. PMID: 32428018 Free PMC article.
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivors.
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. Monda E, et al. Among authors: caiazza m. Eur J Prev Cardiol. 2021 Aug 23;28(10):1134-1137. doi: 10.1177/2047487320940863. Eur J Prev Cardiol. 2021. PMID: 32715753 No abstract available.
112 results