Table 1.

Experience of hepatocyte transplantation in human diseases

Inborn errors of metabolism	Acute liver failure
Acute intermittent porphyria	Acute fatty liver of pregnancy
a1-Antitrypsin deficiency	Drug induced
Crigler-Najjar syndrome	Idiopathic
Factor VII deficiency	Mushroom poisoning
Familial hypercholesterolemia	Post-surgical
Glycogen storage diseases	Viral
Hemochromatosis-hemosiderosis
Hyperlipidemia	Other
Infantile Refsum's disease	Biliary atresia
Primary oxalosis	Cirrhosis
Phenylketonuria
PFIC 2, ABCB11 deficiency, Bile salt exporter pump disease
Tyrosinemia
Urea cycle defects
Ornithine transcarba mylase
deficiency
Argininosuccinate lyase deficiency
Carbamoylphosphate synthase type 1 deficiency
Citrullinemia

PFIC, Progressive familial intrahepatic cholestasis