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mildewed    
n. 霉

霉

Mildew \Mil"dew\, v. t. [imp. & p. p. {Mildewed}; p. pr. & vb.
n. {Mildewing}.]
To taint with mildew; as, mildewed clothing.
[1913 Webster]

He . . . mildews the white wheat. --Shak.
[1913 Webster]


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  • EASL Clinical Practice Guidelines on haemochromatosis
    In patients with high TSAT and elevated ferritin but other HFE genotypes, diagnosis requires the presence of hepatic iron overload on MRI or liver biopsy The stage of liver fibrosis and other end-organ damage should be carefully assessed at diagnosis because they determine disease management
  • EASL Clinical Practice Guidelines on haemochromatosis
    Elevated transferrin saturation and high serum ferritin should prompt HFE genotyping as homozygosity for p C282Y can confirm the diagnosis of haemochromatosis 9 In patients with elevated transferrin saturation who are not homozygous for p C282Y, non-invasive quantification of hepatic iron with MRI is recommended, because patients with haemochromatosis typically have high concentrations of
  • Clinical Practice Guidelines - EASL-The Home of Hepatology.
    The updated EASL Clinical Practice Guidelines on the management of hepatitis B virus (HBV) infection provide comprehensive, evidence-based recommendations for its management
  • Guideline Review: European Association for the Study of Liver (EASL . . .
    The European Association for the Study of the Liver (EASL) has recently (June 2022) produced new clinical practice guidelines for the investigation and management of haemochromatosis, to replace the previous document published in 2010
  • EASL Clinical Practice Guidelines on haemochromatosis
    In patients with high TSAT and elevated ferritin but other HFE genotypes, diagnosis requires the presence of hepatic iron overload on MRI or liver biopsy The stage of liver brosis and fi other end-organ damage should be carefully assessed at diag-nosis because they determine disease management
  • Guideline Review: European Association for the Study of Liver (EASL . . .
    The European Association for the Study of the Liver (EASL) has recently (June 2022) produced new clinical practice guidelines for the investigation and management of haemochromatosis, to replace the previous document published in 2010
  • How to manage a patient with elevated ferritin and abnormal liver enzymes?
    Management of Elevated Liver Enzymes and Ferritin 1000 μg L This patient requires immediate evaluation for hemochromatosis with HFE genetic testing and transferrin saturation, plus consideration for liver biopsy given the combination of ferritin ≥1000 μg L with markedly elevated transaminases (AST 796) 1
  • EASL Clinical Practice Guidelines on haemochromatosis
    In patients with high TSAT and elevated ferritin but other HFE genotypes, diagnosis requires the presence of hepatic iron overload on MRI or liver biopsy The stage of liver fibrosis and other end-organ damage should be carefully assessed at diagnosis because they determine disease management
  • European Association for Study of the Liver (EASL) clinical practice . . .
    A ferritin under 1000 µg L is associated with a minimal risk of liver fibrosis Advances in genetic testing have led to improved diagnosis of rarer genetic types although management can be complex MRI can be used to differentiate primary from secondary cases of iron overload
  • Transferrin Saturation and Serum Ferritin Are Main Predictors of Liver . . .
    Hyperferritinemia is widespread and is caused by or associated with a variety of diseases requiring complex diagnostic workup Magnetic resonance imaging–based liver iron quantification (LICMRI) can differentiate subjects with iron overload requiring treatment but is still limited to specialized centers and costly We aimed to determine whether parameters belonging to the diagnostic setting
  • European Association for Study of the Liver (EASL) clinical practice . . .
    The European Association for the Study of the Liver has recently updated guidance on haemochromatosis with a more extensive discussion on investigation and management [ The new guidance focuses on non-invasive methods for fibrosis assessment and early diagnosis to include more extensive genetic testing if needed Early diagnosis and treatment is vital as it reduces morbidity and mortality We





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