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  1. Article

    Open Access

    Long-term outcome of a patient with Transcobalamin deficiency caused by the homozygous c.1115_1116delCA mutation in TCN2 gene: a case report

    Transcobalamin deficiency is a rare autosomal recessive inborn error of cobalamin transport (prevalence: < 1/1000000) which clinically manifests in early infancy.

    Francesco Martino, Alessandra Magenta… in Italian Journal of Pediatrics (2021)

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    Article

    Ivabradine in Patients with ST-Elevation Myocardial Infarction Complicated by Cardiogenic Shock: A Preliminary Randomized Prospective Study

    An elevated heart rate (HR) is an independent risk factor for mortality and morbidity in patients with acute heart failure (HF). The purpose of this study was to evaluate the impact of ivabradine, a selective ...

    Francesco Barillà, Giuseppe Pannarale, Concetta Torromeo… in Clinical Drug Investigation (2016)

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    Article

    Does cirrhotic cardiomyopathy exist? 50 years of uncertainty

    Subtle abnormalities of cardiac structure or function are often identified in patients with liver cirrhosis and have been termed cirrhotic cardiomyopathy. However, in the absence of a precise definition, its d...

    Pierpaolo Pellicori, Concetta Torromeo, Angela Calicchia… in Clinical Research in Cardiology (2013)

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    Article

    Effects of rosuvastatin on platelet inhibition by clopidogrel in cardiovascular patients

    Statin interference has been suggested among the mechanisms of reduction of the antiplatelet effect of clopidogrel. We thus sought to assess the influence of rosuvastatin on clopidogrel antiplatelet action in ...

    Silvia Riondino, Natalia Petrini… in Journal of Thrombosis and Thrombolysis (2009)