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Autor:
E. Buckel, R. Rebolledo, M. Ferrario, S. Cavallieri, A. Alba, B. Hunter, G. González, H. Auad, J. Godoy, Mario Uribe, C. Acuña, C. Heine
Publikováno v:
Transplantation Proceedings. 45:3731-3733
Background Orthotopic liver transplantation is the treatment of choice for most terminal liver diseases in children. In small children (≤10 kg), this procedure is challenging and has special considerations. The aim of this study is to describe the
Autor:
R. Dalmazzo, C. Heine, M. Campos, C. Valverde, R. Rebolledo, E. Buckel, A. Alba, C. Acuña, R. Zuleta, H. Auad, A. Wash, B. Hunter, C. Herzog, M. Ferrario, L. Calabrán, Mario Uribe, S. Ferrón, J. Godoy, L. Flores, P. Soto, F. Pizarro, L. Macho, V. Díaz, S. Cavallieri, G. González
Publikováno v:
Transplantation proceedings. 45(10)
Introduction In 1994 our group began its experience with pediatric liver transplantation. The experience gained during this period is the largest in the country, positioning the Hospital Luis Calvo Mackenna and Clinica Las Condes as major referral ce
Autor:
B. Hunter, A. Alba, M. Uribe, S. Cavallieri, M. Ferrario, J. Godoy, G. González, L. Macho, S. Ferrón, V. Díaz, R. Iñiguez, E. Buckel
Publikováno v:
Transplantation Proceedings. 40:3253-3255
Living donor liver transplantation (LDLT) for patients with acute liver failure (ALF) is still controversial. To be considered a feasible alternative, this therapeutic option should offer similar results to transplants performed with cadaveric grafts
Autor:
G. González, J. Godoy, S Ceresa, M.T. Santander, S. Cavallieri, B. Hunter, E. Buckel, F Berwart, M. Ferrario, L. Calabrán, M. Uribe, C. Herzog
Publikováno v:
Transplantation Proceedings. 37:3375-3377
Liver transplantation is the only treatment for patients with terminal acute and chronic diseases. Liver transplantation was started in Chile in 1985; our pediatric program began in 1993. The aim of this paper work was to present our experience from
Autor:
P. Soto, A. Alba, C. Herzog, J. Godoy, E. Buckel, M. Ferrario, M. Uribe, S. Cavallieri, C. Valverde, L. Calabrán, R. Rebolledo, B. Hunter, L. Flores
Publikováno v:
Transplantation proceedings. 42(1)
Background. Acute liver failure (ALF) in children is a life-threatening condition, associated with high mortality, and in almost one third of the cases, with no other therapeutic option than orthotopic liver transplant (OLT). The aim of this study wa
Autor:
L. Flores, R. Íñiguez, H. Auad, C. Heine, R. Zuleta, A. Alba, P. Soto, Mario Uribe, B. Hunter, S. Cavallieri, G. González, C. Acuña
Publikováno v:
Transplantation Proceedings. 45:3726-3727
Introduction Pediatric liver transplantation is limited by donation. In the last 5 years, urgent conditions have forced transplant teams to accept donors with minor suboptimal conditions, termed “extended donor criteria.” Among those, the risk of
Autor:
L. Calabrán, G. González, R. Iñiguez, E. Buckel, M. Ferrario, M. Uribe, C. Herzog, J. Godoy, S. Cavallieri, B. Hunter
Publikováno v:
Transplantation proceedings. 39(3)
Introduction. Liver transplantation is the only treatment for end-stage liver disease. Not all patients have a favorable outcome. Graft failure secondary to primary nonfunction, vascular complications, or chronic rejection among other problems may le
Autor:
E. Campusano, B. Ortíz, M. Jorquera, M. Uribe, S. Cavallieri, S. Salas, G. Salazar, B. Hunter, G. González, L. Calabrán
Publikováno v:
Transplantation proceedings. 39(3)
Several psychosocial and behavioral problems have been reported in liver transplanted children. Most publications have focused on them, without considering their family environment. The aim of this study was to evaluate the interaction between liver
Autor:
E. Buckel, M. Uribe, G. González, L. Calabrán, Gladys Smok, S Ceresa, C. Herzog, A Blanco, F Berwart, M. Ferrario, M.T. Santander, S. Cavallieri, B. Hunter, J. Godoy
Publikováno v:
Transplantation proceedings. 37(8)
Living related living transplantation (LRLT) has opened new possibilities for planning transplantation in better conditions for children with emergency situations and chronic liver diseases. Since we began the LRLT program in 1999, we have performed