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Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis

Hepatology (Baltimore, Md.), 2006-05, Vol.43 (5), p.1135-1144

2006

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The melatonin receptor subtype MT1 is expressed in human gallbladder epithelia

Journal of pineal research, 2004-01, Vol.36 (1), p.43-48

2004

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Characterization of Autoantibodies against Components of the Nuclear Pore Complexes

Annals of the New York Academy of Sciences, 2007-08, Vol.1109 (1), p.519-530

2007

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Liver autoimmune serology: a consensus statement from the committee for autoimmune serology of the International Autoimmune Hepatitis Group

Journal of hepatology, 2004-10, Vol.41 (4), p.677-683

2004

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Lack of evidence for involvement of fetal microchimerism in pathogenesis of primary biliary cirrhosis

Digestive diseases and sciences, 2002-09, Vol.47 (9), p.1909-1914

2002

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Spontaneous viral clearance in patients with acute hepatitis C can be predicted by repeated measurements of serum viral load

Hepatology (Baltimore, Md.), 2003, Vol.37 (1), p.60-64

2003

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Primary Sclerosing Cholangitis: New Approaches to Diagnosis, Surveillance and Treatment

Digestive diseases (Basel), 2012-01, Vol.30 (Suppl 1), p.39-47

2012

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Autoantibodies against nuclear pore complexes are associated with more active and severe liver disease in primary biliary cirrhosis

Journal of hepatology, 2001-03, Vol.34 (3), p.366-372

2001

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The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C

Gastroenterology (New York, N.Y. 1943), 1999, Vol.116 (1), p.127-134

1999

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Characterization of autoantibodies against components of the nuclear pore complexes: high frequency of anti-p62 nucleoporin antibodies

Annals of the New York Academy of Sciences, 2007-08, Vol.1109 (1), p.519-530

2007

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Characterization of the antibodies to p62 nucleoporin in primary biliary cirrhosis using human recombinant antigen

Journal of cellular biochemistry, 2008-05, Vol.104 (1), p.27-37

2008

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Prevalence and clinical importance of hypertransaminasaemia in coeliac disease

European journal of gastroenterology & hepatology, 1999-03, Vol.11 (3), p.283-288

1999

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Subcellular localization of the ABCG2 transporter in normal and malignant human gallbladder epithelium

Laboratory investigation, 2004-08, Vol.84 (8), p.1024-1036

2004

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TGF-β1 codon 25 gene polymorphism is associated with cirrhosis in patients with hereditary hemochromatosis

Cytokine (Philadelphia, Pa.), 2005-07, Vol.31 (2), p.142-148

2005

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Association of myeloperoxidase promotor polymorphism with cirrhosis in patients with hereditary hemochromatosis

Journal of hepatology, 2005-06, Vol.42 (6), p.914-919

2005

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Members of the glutathione S-transferase gene family are antigens in autoimmune hepatitis

Gastroenterology (New York, N.Y. 1943), 1998-02, Vol.114 (2), p.329-335

1998

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Treatment of pruritus in chronic liver disease with the 5-hydroxytryptamine receptor type 3 antagonist ondansetron: a randomized, placebo-controlled, double-blind cross-over trial

European journal of gastroenterology & hepatology, 1998-10, Vol.10 (10), p.865-870

1998

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Vanishing Bile Duct Syndrome and Sclerosing Cholangitis in Patients with Critical Illness and Long Term Intensive Care Treatment

Gastrointestinal endoscopy, 2005-04, Vol.61 (5), p.AB206-AB206

2005

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Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

Journal of hepatology, 1997-11, Vol.27 (5), p.773-779

1997

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Autoantibodies from patients with primary biliary cirrhosis preferentially react with the amino-terminal domain of nuclear pore complex glycoprotein gp210

The Journal of experimental medicine, 1995-10, Vol.182 (4), p.1159-1162

1995

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Screening for celiac disease in first-degree relatives of patients with celiac disease by lactulose/mannitol test

The American journal of gastroenterology, 1995-10, Vol.90 (10), p.1838-1842

1995

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Screening for celiac disease : a prospective study on the value of noninvasive tests

The American journal of gastroenterology, 1995-03, Vol.90 (3), p.394-398

1995

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Polymorphism (-463 G/A) of the myeloperoxidase promotor may contribute to fibrosis in hereditary hemochromatosis

Gastroenterology (New York, N.Y. 1943), 2003-04, Vol.124 (4), p.A759-A759

2003

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Centrilobular necrosis in autoimmune hepatitis: A histological feature associated with an acute onset of disease

Gastroenterology (New York, N.Y. 1943), 2003-04, Vol.124 (4), p.A711-A711

2003

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Studies of Sensitivity and Electro-kinetic Potential in Leda Clay

Nature (London), 1964-11, Vol.204 (4960), p.808-809

PENNER, EDWARD

1964

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Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis

The melatonin receptor subtype MT1 is expressed in human gallbladder epithelia

Characterization of Autoantibodies against Components of the Nuclear Pore Complexes

Liver autoimmune serology: a consensus statement from the committee for autoimmune serology of the International Autoimmune Hepatitis Group

Lack of evidence for involvement of fetal microchimerism in pathogenesis of primary biliary cirrhosis

Spontaneous viral clearance in patients with acute hepatitis C can be predicted by repeated measurements of serum viral load

Primary Sclerosing Cholangitis: New Approaches to Diagnosis, Surveillance and Treatment

Autoantibodies against nuclear pore complexes are associated with more active and severe liver disease in primary biliary cirrhosis

The relation of iron status and hemochromatosis gene mutations in patients with chronic hepatitis C

Characterization of autoantibodies against components of the nuclear pore complexes: high frequency of anti-p62 nucleoporin antibodies

Characterization of the antibodies to p62 nucleoporin in primary biliary cirrhosis using human recombinant antigen

Prevalence and clinical importance of hypertransaminasaemia in coeliac disease

Subcellular localization of the ABCG2 transporter in normal and malignant human gallbladder epithelium

TGF-β1 codon 25 gene polymorphism is associated with cirrhosis in patients with hereditary hemochromatosis

Association of myeloperoxidase promotor polymorphism with cirrhosis in patients with hereditary hemochromatosis

Members of the glutathione S-transferase gene family are antigens in autoimmune hepatitis

Treatment of pruritus in chronic liver disease with the 5-hydroxytryptamine receptor type 3 antagonist ondansetron: a randomized, placebo-controlled, double-blind cross-over trial

Vanishing Bile Duct Syndrome and Sclerosing Cholangitis in Patients with Critical Illness and Long Term Intensive Care Treatment

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis

Autoantibodies from patients with primary biliary cirrhosis preferentially react with the amino-terminal domain of nuclear pore complex glycoprotein gp210

Screening for celiac disease in first-degree relatives of patients with celiac disease by lactulose/mannitol test

Screening for celiac disease : a prospective study on the value of noninvasive tests

Polymorphism (-463 G/A) of the myeloperoxidase promotor may contribute to fibrosis in hereditary hemochromatosis

Centrilobular necrosis in autoimmune hepatitis: A histological feature associated with an acute onset of disease

Studies of Sensitivity and Electro-kinetic Potential in Leda Clay

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