Hypertension frequently develops early after liver transplantation when cyclosporine-based immunosuppression is used. However, initial experience with tacrolimus has suggested that its use leads to a lower early incidence of hypertension. In this study, the blood pressure status of patients treated
Studies on mechanisms of augmentation of liver regeneration by cyclosporine and FK 506
β Scribed by Antonio Francavilla; Thomas E. Starzl; Michele Barone; Qi-Hua Zeng; Kendrick A. Porter; Adrianni Zeevi; Peter M. Markus; Marcell R. M. van den Brink; Satoru Todo
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 362 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0270-9139
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The development of atherosclerotic cardiovascular complications is a common and serious problem for the long-term survivors of organ transplantation. Cyclosporine A plus steroid-based immuno-suppression regimens in these patients are associated with the development of hypertension, hyperlipidemia, o
## Abstract Tritiumβlabeled Cyclosporin A (**I**) and FKβ506 (**II**) have been prepared using a metalβcatalysed hydrogen isotope exchange procedure and high specific activity tritiated water. Specific activities of the labeled compounds were 0.15 and 0.59 TBq/mmol, respectively. Copyright Β© 2004 J
Lymphoproliferative disorders (LPDs) are a serious side effect of immunosuppression after liver transplantation, and the introduction on the market of a new immunosuppressive drug has been associated with an increased risk of these disorders. To compare the effect of cyclosporine A (CSA) and FK506 i
Guillain-Barre Β΄syndrome (GBS) has been rarely reported after liver transplantation and generally has good outcome. We report a liver transplant patient on FK506 (tacrolimus) who developed GBS 6 months after liver transplantation. There was no evidence of liver rejection or active infection. Despite
## Abstract We compared the effects of FK506 administration on regeneration and reinnervation after sciatic nerve resection and repair with an autologous graft or with a silicone tube leaving a 6βmm gap in the mouse. Functional reinnervation was assessed by noninvasive methods to determine recovery