International audienceBackground & aims - C282Y homozygotes with serum ferritin (SF) levels >1000 μg/L and/or increased serum transaminase levels are at risk of severe F3/F4 fibrosis. Current practical guidelines recommend liver biopsy in such individuals. This prospective observational cohort study aimed to evaluate non-invasive alternative means such as hyaluronic acid (HA) and transient elastography (TE) for the assessment of severe fibrosis in patients with SF >1000 μg/L or elevated transaminases. Methods - Between September 2005 and April 2013, 77 patients diagnosed C282Y homozygotes underwent a liver biopsy because of SF >1000 μg/L and/or increased transaminases according to current guidelines, with concomitant TE. All of them had cl...
Background: Evaluation of fibrosis is crucial in the assessment of chronic hepatitis C (CHC). The en...
Chronic liver disease is a late stage of progressive hepatic fibrosis. It consists of functional and...
Background & Aims: Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal ...
International audienceC282Y homozygotes with serum ferritin (SF) levels >1000 μg/L and/or increased ...
Abstract Aspartate aminotransferase-to-platelet ratio index (APRI) and Fibrosis-4 Index (Fib4) have ...
Background: DNA-based HFE gene testing can confirm heredi-tary hemochromatosis in most people of Nor...
Diagnosing the presence of cirrhosis is crucial for the management of patients with C282Y hereditary...
Assessment of liver fibrosis is important in determining prognosis, disease progression and need for...
OBJECTIVES: Hepatic fibrosis is a complication of hereditary hemochromatosis. The aim of this study...
The correlation between liver stiffness, measured by transient elastography, liver fibrosis, using t...
Liver fibrosis should be assessed in all individuals with chronic liver disease as it predicts the r...
Transient elastography (TE) is a valuable noninvasive technique of measuring liver stiffness and a r...
BACKGROUND & AIMS: Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal ...
Liver stiffness measurement (LSM) and FibroTest (FT) are frequently used as non-invasive alternative...
International audienceBackground and aims: Accurate biomarkers for quantifying liver fibrosis are im...
Background: Evaluation of fibrosis is crucial in the assessment of chronic hepatitis C (CHC). The en...
Chronic liver disease is a late stage of progressive hepatic fibrosis. It consists of functional and...
Background & Aims: Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal ...
International audienceC282Y homozygotes with serum ferritin (SF) levels >1000 μg/L and/or increased ...
Abstract Aspartate aminotransferase-to-platelet ratio index (APRI) and Fibrosis-4 Index (Fib4) have ...
Background: DNA-based HFE gene testing can confirm heredi-tary hemochromatosis in most people of Nor...
Diagnosing the presence of cirrhosis is crucial for the management of patients with C282Y hereditary...
Assessment of liver fibrosis is important in determining prognosis, disease progression and need for...
OBJECTIVES: Hepatic fibrosis is a complication of hereditary hemochromatosis. The aim of this study...
The correlation between liver stiffness, measured by transient elastography, liver fibrosis, using t...
Liver fibrosis should be assessed in all individuals with chronic liver disease as it predicts the r...
Transient elastography (TE) is a valuable noninvasive technique of measuring liver stiffness and a r...
BACKGROUND & AIMS: Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal ...
Liver stiffness measurement (LSM) and FibroTest (FT) are frequently used as non-invasive alternative...
International audienceBackground and aims: Accurate biomarkers for quantifying liver fibrosis are im...
Background: Evaluation of fibrosis is crucial in the assessment of chronic hepatitis C (CHC). The en...
Chronic liver disease is a late stage of progressive hepatic fibrosis. It consists of functional and...
Background & Aims: Mutations in the hemochromatosis gene (HFE) (C282Y and H63D) lead to parenchymal ...