1
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Two novel mutations, L490R and V561X, of the transferrin receptor 2 gene in Japanese patients with hemochromatosis.
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Haematologica
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2005
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2.12
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2
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Patients with chronic hepatitis C achieving a sustained virological response to peginterferon and ribavirin therapy recover from impaired hepcidin secretion.
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J Hepatol
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2008
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1.85
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3
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A significant reduction in serum alanine aminotransferase levels after 3-month iron reduction therapy for chronic hepatitis C: a multicenter, prospective, randomized, controlled trial in Japan.
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J Gastroenterol
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2004
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1.83
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4
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Long term effects of phlebotomy on biochemical and histological parameters of chronic hepatitis C.
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Am J Gastroenterol
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2002
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1.63
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5
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Current state of Wilson disease patients in central Japan.
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Intern Med
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2010
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1.45
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6
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Potential of the international scoring system for the diagnosis of Wilson disease to differentiate Japanese patients who need anti-copper treatment.
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Hepatol Res
|
2011
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0.87
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7
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A Japanese family with ferroportin disease caused by a novel mutation of SLC40A1 gene: hyperferritinemia associated with a relatively low transferrin saturation of iron.
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Intern Med
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2005
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0.84
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8
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Ursodeoxycholic acid induces glutathione synthesis through activation of PI3K/Akt pathway in HepG2 cells.
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Biochem Pharmacol
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2008
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0.84
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9
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Three patients with middle-age-onset hemochromatosis caused by novel mutations in the hemojuvelin gene.
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J Hepatol
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2005
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0.83
|
10
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Determination of ferritin and hemosiderin iron in patients with normal iron stores and iron overload by serum ferritin kinetics.
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Nagoya J Med Sci
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2012
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0.83
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11
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Biochemical staging of the chronic hepatic lesions of Wilson disease.
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Nagoya J Med Sci
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2014
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0.82
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12
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Additional effect of low iron diet on iron reduction therapy by phlebotomy for chronic hepatitis C.
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Hepatogastroenterology
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2005
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0.82
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13
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Increase in P-glycoprotein accompanied by activation of protein kinase Calpha and NF-kappaB p65 in the livers of rats with streptozotocin-induced diabetes.
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Biochim Biophys Acta
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2008
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0.81
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14
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High prevalence of fulminant hepatic failure among patients with mutant alleles for truncation of ATP7B in Wilson's disease.
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Scand J Gastroenterol
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2010
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0.81
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15
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Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders.
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J Gastroenterol
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2010
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0.81
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16
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Copper- and iron-rich matrices in hepatocellular lipofuscin particles of a young male patient: diagnostic ultrastructures for Wilson disease.
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Ultrastruct Pathol
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2006
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0.80
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17
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Clinicopathological study of Japanese patients with genetic iron overload syndromes.
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Pathol Int
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2012
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0.80
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18
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Identification of a novel mutation in the HAMP gene that causes non-detectable hepcidin molecules in a Japanese male patient with juvenile hemochromatosis.
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Blood Cells Mol Dis
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2012
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0.80
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19
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Potentiation of vasoconstrictor response and inhibition of endothelium-dependent vasorelaxation by gallic acid in rat aorta.
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Planta Med
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2002
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0.79
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20
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Identification of a novel 2026G-->C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndrome.
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J Hum Genet
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2003
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0.78
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21
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Increasing and decreasing phases of ferritin and hemosiderin iron determined by serum ferritin kinetics.
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Nagoya J Med Sci
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2013
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0.78
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22
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Effects of catechins on vascular tone in rat thoracic aorta with endothelium.
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Life Sci
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2002
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0.77
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23
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Hemojuvelin hemochromatosis receiving iron chelation therapy with deferasirox: improvement of liver disease activity, cardiac and hematological function.
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Eur J Haematol
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2011
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0.77
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24
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Hepcidin expression in iron overload diseases is variably modulated by circulating factors.
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PLoS One
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2012
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0.77
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25
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Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan.
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J Gastroenterol
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2005
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0.77
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26
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AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis.
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Hepatol Res
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2003
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0.77
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27
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A male patient with ferroportin disease B and a female patient with iron overload similar to ferroportin disease B.
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Clin J Gastroenterol
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2014
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0.77
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28
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Endothelium-dependent contraction of rat thoracic aorta induced by gallic acid.
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Phytother Res
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2003
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0.75
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29
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Improvement of serum bilirubin levels after venesection in a patient with Dubin-Johnson syndrome and HCV-positive chronic liver disease.
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J Gastroenterol
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2004
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0.75
|
30
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Reduction of MDR3 mRNA levels by forskolin in Chang liver cells.
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Anticancer Res
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2003
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0.75
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31
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Investigation of the structure of cellulose in LiCl/DMAc solution and its gelation behavior by small-angle X-ray scattering measurements.
|
Macromol Biosci
|
2006
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0.75
|
32
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Mutation analysis of the multidrug resistance protein 2 (MRP2) gene in a Japanese patient with Dubin-Johnson syndrome.
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Hepatol Res
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2004
|
0.75
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33
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Two male patients with Wilson's disease treated using trientine and iron reduction therapy.
|
J Gastroenterol Hepatol
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2005
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0.75
|
34
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Preliminary study of spontaneous hepatitis in Long-Evans Cinnamon rats: a blood exchange may improve fetal hepatitis.
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Nagoya J Med Sci
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2010
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0.75
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35
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Protein kinase Cbeta isoform down-regulates the expression of MDR3 P-glycoprotein in human Chang liver cells.
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Biochim Biophys Acta
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2006
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0.75
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36
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[Iron reduction therapy by phlebotomy for chronic hepatitis C].
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Nihon Rinsho
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2011
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0.75
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