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  1. No Access

    Article

    A global survey on the use of the international classification of diseases codes for metabolic dysfunction-associated fatty liver disease

    With the implementation of the 11th edition of the International Classification of Diseases (ICD-11) and the publication of the metabolic dysfunction-associated fatty liver disease (MAFLD) nomenclature in 2020...

    Huai Zhang, Giovanni Targher, Christopher D. Byrne in Hepatology International (2024)

  2. Article

    Open Access

    The contribution of genetics and epigenetics to MAFLD susceptibility

    Metabolic dysfunction-associated fatty liver disease (MAFLD) is the most common liver disease worldwide. The risk of develo** MAFLD varies among individuals, due to a combination of environmental inherited a...

    Vittoria Moretti, Stefano Romeo, Luca Valenti in Hepatology International (2024)

  3. Article

    Open Access

    Author Correction: Interaction between estrogen receptor-α and PNPLA3 p.I148M variant drives fatty liver disease susceptibility in women

    Alessandro Cherubini, Mahnoosh Ostadreza, Oveis Jamialahmadi in Nature Medicine (2024)

  4. Article

    Author Correction: Consensus Statement on the definition and classification of metabolic hyperferritinaemia

    Luca Valenti, Elena Corradini, Leon A. Adams, Elmar Aigner in Nature Reviews Endocrinology (2024)

  5. No Access

    Article

    Recompensation in cirrhosis: unravelling the evolving natural history of nonalcoholic fatty liver disease

    Recompensation has gained increasing attention in the field of cirrhosis, particularly in chronic liver disease with a definite aetiology. The current global prevalence of obesity and nonalcoholic fatty liver ...

    Gong Feng, Luca Valenti in Nature Reviews Gastroenterology & Hepatolo… (2024)

  6. 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)

  7. Article

    Open Access

    Interaction between estrogen receptor-α and PNPLA3 p.I148M variant drives fatty liver disease susceptibility in women

    Fatty liver disease (FLD) caused by metabolic dysfunction is the leading cause of liver disease and the prevalence is rising, especially in women. Although during reproductive age women are protected against F...

    Alessandro Cherubini, Mahnoosh Ostadreza, Oveis Jamialahmadi in Nature Medicine (2023)

  8. Article

    Open Access

    Incidence, microbiological and immunological characteristics of ventilator-associated pneumonia assessed by bronchoalveolar lavage and endotracheal aspirate in a prospective cohort of COVID-19 patients: CoV-AP study

    No univocal recommendation exists for microbiological diagnosis of ventilator-associated pneumonia (VAP). Sampling of either proximal or distal respiratory tract likely impacts on the broad range of VAP incide...

    Davide Mangioni, Mauro Panigada, Emanuele Palomba, Chiara Bobbio in Critical Care (2023)

  9. Article

    Consensus Statement on the definition and classification of metabolic hyperferritinaemia

    Hyperferritinaemia is a common laboratory finding that is often associated with metabolic dysfunction and fatty liver. Metabolic hyperferritinaemia reflects alterations in iron metabolism that facilitate iron ...

    Luca Valenti, Elena Corradini, Leon A. Adams, Elmar Aigner in Nature Reviews Endocrinology (2023)

  10. 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)

  11. 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)

  12. 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)

  13. Article

    Open Access

    PSD3 downregulation confers protection against fatty liver disease

    Fatty liver disease (FLD) is a growing health issue with burdening unmet clinical needs. FLD has a genetic component but, despite the common variants already identified, there is still a missing heritability c...

    Rosellina M. Mancina, Kavitha Sasidharan, Anna Lindblom, Ying Wei in Nature Metabolism (2022)

  14. Article

    Advancing the global public health agenda for NAFLD: a consensus statement

    Non-alcoholic fatty liver disease (NAFLD) is a potentially serious liver disease that affects approximately one-quarter of the global adult population, causing a substantial burden of ill health with wide-rang...

    Jeffrey V. Lazarus, Henry E. Mark in Nature Reviews Gastroenterology & Hepatolo… (2022)

  15. Article

    Open Access

    Targeting of eIF6-driven translation induces a metabolic rewiring that reduces NAFLD and the consequent evolution to hepatocellular carcinoma

    A postprandial increase of translation mediated by eukaryotic Initiation Factor 6 (eIF6) occurs in the liver. Its contribution to steatosis and disease is unknown. In this study we address whether eIF6-driven ...

    Alessandra Scagliola, Annarita Miluzio, Gabriele Ventura in Nature Communications (2021)

  16. Article

    Open Access

    Adipocyte PHLPP2 inhibition prevents obesity-induced fatty liver

    Increased adiposity confers risk for systemic insulin resistance and type 2 diabetes (T2D), but mechanisms underlying this pathogenic inter-organ crosstalk are incompletely understood. We find PHLPP2 (PH domai...

    Kyeong** Kim, ** Ku Kang, Young Hoon Jung, Sang Bae Lee in Nature Communications (2021)

  17. No Access

    Article

    NAFLD in children: new genes, new diagnostic modalities and new drugs

    Nonalcoholic fatty liver disease (NAFLD) has rapidly become the most common form of chronic liver disease in children and adolescents. Over the past 5 years, developments have revolutionized our understanding ...

    Valerio Nobili, Anna Alisi, Luca Valenti in Nature Reviews Gastroenterology & Hepatolo… (2019)

  18. Article

    Open Access

    The TM6SF2 E167K genetic variant induces lipid biosynthesis and reduces apolipoprotein B secretion in human hepatic 3D spheroids

    There is a high unmet need for develo** treatments for nonalcoholic fatty liver disease (NAFLD), for which there are no approved drugs today. Here, we used a human in vitro disease model to understand mechanism...

    Sebastian Prill, Andrea Caddeo, Guido Baselli, Oveis Jamialahmadi in Scientific Reports (2019)

  19. Article

    Open Access

    The effect of the TM6SF2 E167K variant on liver steatosis and fibrosis in patients with chronic hepatitis C: a meta-analysis

    The impact of Transmembrane 6 superfamily member 2 (TM6SF2) E167K variant, which causes hepatocellular fat retention by altering lipoprotein secretion, on liver damage and metabolic traits in chronic hepatitis C ...

    Zhengtao Liu, Shu** Que, Lin Zhou, Shusen Zheng, Stefano Romeo in Scientific Reports (2017)

  20. Article

    Open Access

    MBOAT7 rs641738 variant and hepatocellular carcinoma in non-cirrhotic individuals

    Nonalcoholic fatty liver disease (NAFLD) represents an emerging cause of hepatocellular carcinoma (HCC), especially in non-cirrhotic individuals. The rs641738 C > T MBOAT7/TMC4 variant predisposes to progressive ...

    Benedetta Donati, Paola Dongiovanni, Stefano Romeo, Marica Meroni in Scientific Reports (2017)

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