Hepatocyte transplantation in hereditary coagulation factor VII deficiency

References

[1] Fox I.J. et al. Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation. N Engl J Med 1998; 338: 1422-6.

[2] Sokal E. et al. Hepatocyte transplantation in a 4-year-old girl with peroxisomal biogenesis disease: technique, safety, and metabolic follow-up. Transplantation 2003; 76: 735—8.

[3] Mitry R.R. et a. One liver, three recipients: segment IV from split-liver procedures as a source of hepatocytes for cell transplantation. Transplantation 2004; 77; 10: 1614-6.

[4] Horslen S.P. et al. Isolated hepatocyte transplantation in an infant with a severe urea cycle disorder. Pediatrics 2003; 111: 1262—7.

[5] Muraca M. et al. Hepatocyte transplantation as a treatment for glycogen storage disease type 1a. Lancet 2002;359:317-8.

[6] Darwish A.A. et al. Permanent access to the portal system for cellular transplantation using an implantable port device. Liver Transpl 2004; 10; 9: 1213—5.

[7] Mitry R.R. et al. Human hepatocyte isolation and relationship of cell viability to early graft function. Cell Transplant 2003; 12: 69.

[8] Levi D. et al. Liver transplantation for factor VII deficiency. Transplantation 2001; 72: 1836.

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