Takao Saito fut un mangaka célébré et le créateur de l'emblématique Golgo 13. Son travail se distingue par une exécution artistique méticuleuse et une exploration profonde de la psychologie des personnages, lui assurant une place significative dans l'histoire du manga. L'héritage de Saito réside dans sa narration magistrale et son impact sur les genres des bandes dessinées d'action et d'espionnage.
1946: Amidst so many dead in the postwar ruins of Japan, the brutal murder of five members of the same family still has the power to shock--and even more so 29 years later, when the unsolved crime may point to the origins of Duke Togo! Then, the 2000 U.S. presidential election comes down to a handful of recounted ballots in Florida. But the decisive vote will be cast by a bullet from Golgo 13! Plus, FILE 13 concludes VIZ Media's edition of Golgo 13 with an afterword from the Japanese editors of the series!
1976: When congressional hearings expose a CIA chemical warfare program, Golgo is tasked to destroy the evidence on a hellish Pacific island--where he faces a showdown with one of the few men he could call an equal! Then, in 1974, the Deep South gets a visit from Golgo when Black Power activists hire him for a job in Mississippi that reveals him to be one bad brother! Plus FILE 13 tallies up the awesome balance sheet--just how much cash has G13 made in a career of killing?
This book offers a detailed review of the pathological and imaging features, diagnosis and treatment of IgG4-Related Kidney Disease (IgG4-RKD). IgG4-related disease (IgG4-RD), which is characterized by an elevated serum IgG4 level and infiltration of systemic organs by IgG4 positive plasma cells, is a newly recognized systemic disease. Diverse renal manifestations including specific tubulointerstitial nephritis, membranous nephropathy, and tumor-like urological diseases extending to the pelvis and urinary tract in IgG4-RD have been reported and are recently attracting attention as IgG4-RKD. In this book, leading researchers in the field present the latest insights into the broad spectrum of IgG4-RKD characteristics. In addition, they provide a detailed explanation of the pathology of IgG4-RKD including comparisons between the kidney and other affected organs, such as the lacrimal, salivary glands and pancreas in the histopathological section. IgG4-Related Kidney Disease will have a major impact on future immunological and nephrological studies and offers a useful resource not only for nephrologists but also general physicians and investigators in related fields.
