Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Elevated transferrin saturation"'
Publikováno v:
European Journal of Gastroenterology & Hepatology. 34:316-323
OBJECTIVE To determine whether a low aspartate aminotransferase (AST) to alanine aminotransferase (ALT) ratio (AST/ALT ratio) is associated with insulin resistance among those without liver dysfunction. METHODS In this cross-sectional study of the Na
Autor:
Paul C. Adams, James C. Barton
Publikováno v:
Can Liver J
Background: Elevated transferrin saturation (TS) is an imperfect test to identify adults with high-iron gene ( HFE) p.C282Y homozygosity or elevated hepatic iron concentration. Methods: We analyzed observations of non-screening, previously untreated
Akademický článek
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Publikováno v:
Journal of Clinical and Experimental Hepatology. 7:269-273
Elevated serum ferritin level is a common finding in iron overload syndrome, autoimmune and viral hepatitis, alcoholic and nonalcoholic fatty liver diseases. High transferrin saturation is not a common finding in above diseases except for iron overlo
Autor:
Hakan Çam, Nimet Yılmaz
Publikováno v:
Arab journal of gastroenterology : the official publication of the Pan-Arab Association of Gastroenterology. 21(2)
The clinical significance of serum parameters of iron metabolism and hepcidin in liver disease remains unknown. Therefore, this study aimed to evaluate the association of serum hepcidin levels with fibrosis stage and serum iron parameters in patients
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Publikováno v:
Laboratory medicine. 50(2)
Hereditary hemochromatosis (HH) is an autosomal recessive disorder of iron metabolism characterized by increased iron absorption and tissue deposition. Three loss-of-function mutations in the hemochromatosis gene (HFE), namely, C282Y (c.845G>A), H63D
Publikováno v:
Diabetes/Metabolism Research and Reviews. 30:372-394
The literature on the role of body iron status in the development of type 2 diabetes (T2D) in humans is inconsistent. We aimed to assess the association between iron indices and T2D by a meta-analysis of previously published studies. A systematic lit
Autor:
Yves Deugnier, Martine Ropert, Patricia Leroyer, Lénaïck Détivaud, Caroline Le Lan, Annick Mosser, Véronique David, Pierre Brissot, Edouard Bardou-Jacquet, Olivier Loréal, Marie-Laure Island, Anne-Marie Jouanolle
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2013, 34 (11), pp.1529-36. ⟨10.1002/humu.22396⟩
Human Mutation, 2013, 34 (11), pp.1529-36. ⟨10.1002/humu.22396⟩
Human Mutation, Wiley, 2013, 34 (11), pp.1529-36. ⟨10.1002/humu.22396⟩
Human Mutation, 2013, 34 (11), pp.1529-36. ⟨10.1002/humu.22396⟩
International audience; Ferroportin (FPN) mediates iron export from cells and this function is modulated by serum hepcidin. Mutations in the FPN gene (SLC40A1) lead to autosomal dominant iron overload diseases related either to loss or to gain of fun
Autor:
Anne Tybjærg-Hansen, Henrik Ullitis Andersen, Christina Ellervik, Henrik Birgens, Merete Frandsen, Thomas Mandrup-Poulsen, Børge G. Nordestgaard
Publikováno v:
Diabetes Care
OBJECTIVE It is not known to what extent iron overload predicts prognosis in patients with diabetes after diagnosis or whether iron overload is a risk factor independent of the HFE genotype. We investigated total and cause-specific mortality accordin