27 research outputs found
The Electrical-Thermal Switching in Carbon Black-Polymer Composites as a Local Effect
Following the lack of microscopic information about the intriguing well-known
electrical-thermal switching mechanism in Carbon Black-Polymer composites, we
applied atomic force microscopy in order to reveal the local nature of the
process and correlated it with the characteristics of the widely used
commercial switches. We conclude that the switching events take place in
critical interparticle tunneling junctions that carry most of the current. The
macroscopic switched state is then a result of a dynamic-stationary state of
fast switching and slow reconnection of the corresponding junctions.Comment: 14 pages, 5 figures,Typographic correctio
Hepatic Iron Overload following Liver Transplantation from a C282Y/H63D Compound Heterozygous Donor
Hereditary hemochromatosis (HH) is a genetic disease associated with progressive iron overload, eventually leading in some cases to damage of parenchymal organs, such as the liver, pancreas, and heart. Although the gene had been identified (HFE), HH pathogenesis remains to be fully elucidated. We report here, for the first time, a case of inadvertent transplantation of a liver from a donor with C282Y/H63D compound heterozygosity into a nonhemochromatotic 19-year-old Caucasian male recipient with primary sclerosing cholangitis. Progressive iron overload occurred over 1.5 years, as observed in liver biopsies and iron studies, after ruling out secondary causes of iron overload. This case strengthens the hypothesis that the liver, rather than the small intestine, plays a primary role in the maintenance of iron homeostasis
Hepatic Iron Overload following Liver Transplantation from a C282Y/H63D Compound Heterozygous Donor
Hereditary hemochromatosis (HH) is a genetic disease associated with progressive iron overload, eventually leading in some cases to damage of parenchymal organs, such as the liver, pancreas, and heart. Although the gene had been identified (HFE), HH pathogenesis remains to be fully elucidated. We report here, for the first time, a case of inadvertent transplantation of a liver from a donor with C282Y/H63D compound heterozygosity into a nonhemochromatotic 19-year-old Caucasian male recipient with primary sclerosing cholangitis. Progressive iron overload occurred over 1.5 years, as observed in liver biopsies and iron studies, after ruling out secondary causes of iron overload. This case strengthens the hypothesis that the liver, rather than the small intestine, plays a primary role in the maintenance of iron homeostasis