Search Results - "Tavill, Anthony"

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    Liver Disease in Alpha 1-Antitrypsin Deficiency: A Review by FAIRBANKS, Kyrsten D, TAVILL, Anthony S

    Published in The American journal of gastroenterology (01-08-2008)
    “…Alpha 1-antitrypsin deficiency is an inherited metabolic disorder that predisposes the affected individual to chronic pulmonary disease, in addition to chronic…”
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    Journal Article
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    Connective Tissue Diseases and the Liver by Youssef, Wael I, Tavill, Anthony S

    Published in Journal of clinical gastroenterology (01-10-2002)
    “…Connective tissue diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis, Sjögren's syndrome, and scleroderma are systemic disorders that…”
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    Alcohol and iron by Tavill, Anthony S, Qadri, Asif M

    Published in Seminars in liver disease (01-08-2004)
    “…Iron in its free ferrous and ferric states may serve as a physiological regulator of normal intracellular functions but can be a double-edged sword when linked…”
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    Concomitant presentation of collagenous sprue and HFE hemochromatosis by Parisian, Keely R, Plesec, Thomas P, Fairbanks, Kyrsten D, Tavill, Anthony S, Shen, Bo

    Published in Journal of Crohn's and colitis (01-08-2011)
    “…Collagenous sprue (CS) is a progressive malabsorptive disorder characterized by collagen deposition beneath the basement membrane of small bowel epithelium in…”
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    Hepatitis C and Human Immunodeficiency Virus Coinfections by Dodig, Milan, Tavill, Anthony S

    Published in Journal of clinical gastroenterology (01-11-2001)
    “…Hepatitis C virus (HCV) has become a major contributor to morbidity and mortality in patients with human immunodeficiency virus (HIV). It is estimated that 30%…”
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    A diagnostic approach to hemochromatosis by Tavill, Anthony S, Adams, Paul C

    Published in Canadian journal of gastroenterology (01-08-2006)
    “…In the present clinical review, a diagnostic approach to hemochromatosis is discussed from the perspective of two clinicians with extensive experience in this…”
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    Clinical Implications of the Hemochromatosis Gene by Tavill, Anthony S

    Published in The New England journal of medicine (02-09-1999)
    “…Hereditary hemochromatosis is the most common genetic disorder in whites. The prevalence of this condition (i.e., of homozygosity for the faulty gene) in the…”
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    Disordered energy and protein metabolism in liver disease by McCullough, A J, Tavill, A S

    Published in Seminars in liver disease (01-11-1991)
    “…Although progress has been made, more information is needed on the role of nutritional therapy in liver disease. Because considerable heterogeneity exists…”
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    Role of the liver in normal iron metabolism by Bacon, B R, Tavill, A S

    Published in Seminars in liver disease (01-08-1984)
    “…An integrated approach to normal hepatic iron metabolism requires an understanding of the complex interactions between the dynamic processes of iron uptake,…”
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    Obesity and Non-Alcoholic Fatty Liver Disease in Chronic Hepatitis C by Younossi, Zobair M, McCullough, Arthur J, Ong, Janus P, Barnes, David S, Post, Anthony, Tavill, Anthony, Bringman, Diane, Martin, Lisa M, Assmann, Jennifer, Gramlich, Terry, Mullen, Kevin D, O’Shea, Robert, Carey, William D, Ferguson, Roy

    Published in Journal of clinical gastroenterology (01-09-2004)
    “…BACKGROUNDSuperimposed non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) may affect HCV-related fibrosis. We performed a study…”
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    Intracellular pathways of protein synthesis and secretion in the hepatocyte by Tavill, A S

    Published in Seminars in liver disease (01-01-1985)
    “…The multiplicity of data summarized in this review indicate a variety of signals built into the intrinsic structure of secretory, membrane-associated, and…”
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    Editorial: Clinical implications of the hemochromatosis gene by Tavill, Anthony S

    Published in The New England journal of medicine (02-09-1999)
    “…The development of iron overload in HFE knockout mice4 further attested to the role of the gene in the regulation of body iron. Since the C282Y mutation is…”
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