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  1. Article

    Open Access

    Population-based prevalence and mutational landscape of von Willebrand disease using large-scale genetic databases

    Von Willebrand disease (VWD) is a common bleeding disorder caused by mutations in the von Willebrand factor gene (VWF). The true global prevalence of VWD has not been accurately established. We estimated the worl...

    Omid Seidizadeh, Andrea Cairo, Luciano Baronciani, Luca Valenti in npj Genomic Medicine (2023)

  2. Article

    Open Access

    Correction to: Usefulness of Fibrosis-4 (FIB-4) score and metabolic alterations in the prediction of SARS-CoV-2 severity

    Rosa Lombardi, Vincenzo La Mura, Annalisa Cespiati in Internal and Emergency Medicine (2022)

  3. Article

    Open Access

    Usefulness of fibrosis-4 (FIB-4) score and metabolic alterations in the prediction of SARS-CoV-2 severity

    Despite vaccination programs, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains a public health problem. Identifying key prognostic determinants of severity of the disease may help...

    Rosa Lombardi, Vincenzo La Mura, Annalisa Cespiati in Internal and Emergency Medicine (2022)

  4. Article

    Metabolic and genetic determinants for progression to severe liver disease in subjects with obesity from the UK Biobank

    Obesity is among the main determinants of nonalcoholic fatty liver disease progression towards severe liver disease (SLD). However, risk factors for SLD in individuals with obesity have not been examined.

    Antonio De Vincentis, Federica Tavaglione in International Journal of Obesity (2022)

  5. Article

    Open Access

    The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis

    Aim of this study was to evaluate whether the A736V TMPRSS6 polymorphism, a major genetic determinant of iron metabolism in healthy subjects, influences serum levels of hepcidin, the hormone regulating iron me...

    Serena Pelusi, Domenico Girelli, Raffaela Rametta, Natascia Campostrini in BMC Nephrology (2013)

  6. Article

    Open Access

    The i148m Pnpla3 polymorphism influences serum adiponectin in patients with fatty liver and healthy controls

    Reduced adiponectin is implicated in the pathogenesis of nonalcoholic fatty liver disease (NAFLD) and steatohepatitis (NASH), and the I148M Patatin-like phospholipase domain-containing 3 (PNPLA3) polymorphism pre...

    Luca Valenti, Raffaela Rametta, Massimiliano Ruscica in BMC Gastroenterology (2012)

  7. Article

    Open Access

    Lack of association between peroxisome proliferator-activated receptors alpha and gamma2 polymorphisms and progressive liver damage in patients with non-alcoholic fatty liver disease: a case control study

    Peroxisome proliferator-activated receptors (PPARs) play key roles in the pathogenesis of nonalcoholic fatty liver disease (NAFLD).

    Paola Dongiovanni, Raffaela Rametta, Anna Ludovica Fracanzani in BMC Gastroenterology (2010)

  8. No Access

    Article

    The immunopathogenesis of alcoholic and nonalcoholic steatohepatitis: two triggers for one disease?

    Alcoholic liver disease and nonalcoholic liver disease represent a leading cause of liver disease and share similar pathogenic mechanisms among which activation of the immune system plays a key role. The main ...

    Luca Valenti, Anna Ludovica Fracanzani, Silvia Fargion in Seminars in Immunopathology (2009)

  9. No Access

    Article

    Can nonalcoholic steatohepatitis trigger porphyria cutanea tarda clinical manifestations?

    Luca Valenti, Anna Ludovica Fracanzani in Internal and Emergency Medicine (2009)