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J Inherit Metab Dis
January 2007
Hôpital Bicêtre, Inserm U 804 and University Paris XI, le Kremlin-Bicêtre, France.
Transplantation of allogeneic or genetically modified autologous hepatocytes may be an alternative to whole-liver transplantation for the treatment of hereditary metabolic liver diseases. Human hepatocytes have already been transplanted in patients, demonstrating the safety and feasibility of both approaches. Although a few cases of allogeneic transplantation have resulted in long-term engraftment and function, only a partial and transient correction of the disease was achieved.
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