Search Results - "Lenato, Gennaro Mariano"
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Characterization of epidemiological distribution and outcome of COVID-19 in patients with hereditary hemorrhagic telangiectasia: a nationwide retrospective multi-centre study during first wave in Italy
Published in Orphanet journal of rare diseases (08-09-2021)“…Abstract Background Coronavirus Disease 2019 (COVID-19) continues to have a devastating impact across the world. A number of pre-existing common clinical…”
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Erratum to “Hypogonadotropic Hypogonadism Associated with Hereditary Hemorrhagic Telangiectasia”
Published in Case reports in endocrinology (01-01-2013)Get full text
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Significant burden of post-COVID exertional dyspnoea in a South-Italy region: knowledge of risk factors might prevent further critical overload on the healthcare system
Published in Frontiers in public health (21-12-2023)“…Exertional dyspnoea in post-COVID syndrome is a debilitating manifestation, requiring appropriate comprehensive management. However, limited-resources…”
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Hypogonadotropic hypogonadism associated with hereditary hemorrhagic telangiectasia [corrected]
Published in Case reports in endocrinology (2013)“…A 65-year-old man was referred to our clinic for the rehabilitation of right hemiparesis caused by ischaemic stroke. Hypertension, postphlebitic syndrome of…”
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Hypogonadotropic Hypogonadism Associated with Hereditary Hemorrhagic Telengiectasia
Published in Case reports in endocrinology (01-01-2013)“…A 65-year-old man was referred to our clinic for the rehabilitation of right hemiparesis caused by ischaemic stroke. Hypertension, postphlebitic syndrome of…”
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Translational insight into prothrombotic state and hypercoagulation in nonalcoholic fatty liver disease
Published in Thrombosis research (01-02-2021)“…Non-alcoholic fatty liver disease (NAFLD) is an emerging and threatening pathological condition, ranging from fatty liver (FL) to chronic steatohepatitis…”
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Minimal portosystemic encephalopathy: A new nosological entity in patients with hereditary haemorrhagic telangiectasia
Published in European journal of internal medicine (01-08-2021)“…•Hepatic vascular malformations (HVMs) observed in HHT include portosystemic shunts.•The presence of radiologically undetectable HVMs is reported in the…”
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Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study
Published in Digestive and liver disease (01-07-2013)“…Abstract Background Germline mutations in the STK11/LKB1 gene cause Peutz–Jeghers syndrome, an autosomal-dominantly inherited condition characterized by…”
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Impact of SARS-CoV-2 infection in patients with hereditary hemorrhagic telangiectasia: epidemiological and clinical data from the comprehensive Italian retrospective multicenter study
Published in Internal and emergency medicine (01-06-2023)“…Rare Disease patients manifested high concern regarding the possible increased risk of severe outcomes and worsening of disease-specific clinical manifestation…”
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New signs and old applications of echo-color-Doppler should always be compared to a gold standard
Published in Journal of hepatology (01-10-2008)Get full text
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