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Georg Strohmeyer

Researcher at University of Düsseldorf

Publications -  145
Citations -  6291

Georg Strohmeyer is an academic researcher from University of Düsseldorf. The author has contributed to research in topics: Hemochromatosis & Cirrhosis. The author has an hindex of 34, co-authored 145 publications receiving 6143 citations. Previous affiliations of Georg Strohmeyer include San Francisco General Hospital & University of California, San Francisco.

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Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis.

TL;DR: It is concluded that patients with hemochromatosis diagnosed in the precirrhotic stage and treated by venesection have a normal life expectancy, whereas cirrhotic patients have a shortened life expectancy and a high risk of liver cancer even when complete iron depletion has been achieved.
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Long-term survival in patients with hereditary hemochromatosis.

TL;DR: Prognosis of hemochromatosis and most of its complications, including liver cancer, depend on the amount and duration of iron excess, and early diagnosis and therapy largely prevent the adverse consequences of iron overload.
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Isolation and partial characterization of a fatty acid binding protein in rat liver plasma membranes

TL;DR: Immunofluorescence studies localized the antigen in liver-cell plasma membranes as well as in other major sites of fatty acid transport, compatible with the hypothesis that this protein may act as a receptor in a hepatocellular uptake mechanism for fatty acids.
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Pathogenesis of glucose intolerance and diabetes mellitus in cirrhosis

TL;DR: In conclusion, diabetes mellitus in insulinresistant cirrhotic patients develops as the result of progressive impairment in insulin secretion together with the development of hepatic insulin resistance leading to fasting hyperglycemia and a diabetic glucose tolerance profile.
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Wilson disease: clinical presentation, treatment, and survival.

TL;DR: Treatment with D-penicillamine improved most of the hematologic and neurologic abnormalities but had little effect on hepatomegaly and splenomeGaly and did not reverse cirrhosis in patients with Wilson disease.