スポンサーリンク
Department Of Gastroenterology And Hepatology Kyoto Prefectural University Of Medicine | 論文
- Relapse of hepatitis C in a pegylated-interferon-α-2b plus ribavirin-treated sustained virological responder
- Guidelines for the antiviral therapy of hepatitis C virus carriers with normal serum aminotransferase based on platelet counts
- Spatial and chronological differences in hepatitis B virus genotypes from patients with acute hepatitis B in Japan
- 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
- Analysis of hepatic genes involved in the metabolism of fatty acids and iron in nonalcoholic fatty liver disease
- HEPATOBILIARY SARCOIDOSIS : TYPICAL APPEARANCE IN LAPAROSCOPY
- Lower circulating levels of dehydroepiandrosterone, independent of insulin resistance, is an important determinant of severity of non-alcoholic steatohepatitis in Japanese patients
- Predictive values of amino acid sequences of the core and NS5A regions in antiviral therapy for hepatitis C : a Japanese multi-center study
- Adenoendocrine cell carcinoma of the gallbladder clinically mimicking squamous cell carcinoma
- Confirmation of Diabetes-Related Quantitative Trait Loci Derived from SM/J and A/J Mice by Using Congenic Strains Fed a High-Carbohydrate or High-Fat Diet
- Elevation of serum thioredoxin levels in patients with nonalcoholic steatohepatitis
- Special stain and X-ray probe microanalysis of livers with Wilson disease
- Genetic background of Japanese patients with adult-onset storage diseases in the liver
- Compound overload of copper and iron in patients with Wilson's disease
- Iron removal by phlebotomy for the prophylaxis of fulminant hepatitis in a Wilson disease model of Long-Evans Cinnamon Rats
- Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan
- A Japanese Family with Ferroportin Disease Caused by a Novel Mutation of SLC40A1 Gene: Hyperferritinemia Associated with a Relatively Low Transferrin Saturation of Iron
- Mutation analysis of the multidrug resistance protein 2 (MRP2) gene in a Japanese patient with Dubin-Johnson syndrome
- Improvement of serum bilirubin levels after venesection in a patient with Dubin-Jonson syndrome and HCV-positive chronic liver disease
- Identification of a novel 2026G→C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndrome