Titlebook: Autoimmune Liver Diseases; Perspectives from Ja Hiromasa Ohira Book 2014 Springer Japan 2014 AIH.PBC.autoimmune hepatitis.primary biliary c

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https://doi.org/10.1007/978-3-658-19289-1FSF15) and B cell differentiation into plasma cells (IL7R, CXCR5, SPIB, IKZF3, and POU2AF1) between individuals of European descent and Japanese individuals. Most of these disease susceptibility genes are not specific for PBC; they are shared with various other autoimmune diseases. Further studies o

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,Typische Größe von Konzernzentralen, by liver disease has decreased. The 5-year survival rates were 97.9 and 80.3 %, the 10-year survival rate 93.7 and 66.7 %, and the 20-year survival rate 84.2 and 52.1 %, respectively, showing significant differences among the groups (. < 0.0001). As results of examining changes in survival rate of

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Notwendigkeit und Aussagegehalt der Studie,e degree of both chronic cholangitis activity (CA) and hepatitic activity (HA) for grading disease activity were also proposed. Our recent study demonstrated that this new system provides more information, which is consistent with clinical laboratory data and a better reflection of the prognosis of

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https://doi.org/10.1007/978-3-322-99713-5d use of particular ANAs in conjunction with an AMA should be advantageous for accurate and precise diagnoses and even for disease outcomes. The PBC landscape has been steadily changing with the progress in autoantibody research.

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lso recently been discovered. Because of the relatively homogeneous population of Japan, analyses conducted with Japanese PBC patients have yielded findings that are highly relevant to the pathogenesis of the d978-4-431-56171-2978-4-431-54789-1

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Book 2014e liver diseases. Although these disorders are relatively rare, they are recognized as an important group of refractory liver diseases, the most common of which are autoimmune hepatitis (AIH) and primary biliary cirrhosis (PBC). The book therefore comprises two major sections, one dealing with AIH,

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Diagnosis of Autoimmune Hepatitis Because a recently conducted nationwide survey on AIH in Japan has revealed clinical pathological conditions that are different from those previously known, new diagnostic criteria have been issued. This section reviews the diagnosis of AIH mainly on the basis of the new Japanese diagnostic criteria.