Liver after hepatocyte transplantation for liver-based metabolic disorders in children

Cell Transplantation

Volumn 17, Issue 12, 2008, Pages 1403-1414

  Quaglia, Alberto ^a   Lehec, Sharon C ^a   Hughes, Robin D ^a   Mitry, Ragai R ^a   Knisely, A S ^a   Devereaux, Stephen ^a   Richards, Julie ^a   Rela, Mohamed ^a   Heaton, Nigel D ^a   Portmann, Bernard C ^a   Dhawan, Anil ^a  

^a KING S COLLEGE HOSPITAL   (United Kingdom)

Author keywords

Crigler Najjar syndrome; Engraftment; Factor VII deficiency; Ornithine transcarbamylase deficiency; Progressive familial intrahepatic cholestasis type 2 (PFIC 2)

Indexed keywords

ARTICLE; BLOOD CLOTTING FACTOR 7 DEFICIENCY; CLINICAL ARTICLE; CONTROLLED STUDY; CRIGLER NAJJAR SYNDROME; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; EXPLANT; FEMALE; HEPATITIS; HEPATOCYTE TRANSPLANTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INFANT; INTRAHEPATIC CHOLESTASIS; LASER CAPTURE MICRODISSECTION; LIVER ATROPHY; LIVER DISEASE; LIVER HISTOLOGY; MALE; NEWBORN; PHENOTYPE; PORTAL VEIN THROMBOSIS; PRIORITY JOURNAL;

ATROPHY; BIOPSY, NEEDLE; BLOOD PRESSURE; CELL SEPARATION; CELL TRANSPLANTATION; CHILD; CHILD, PRESCHOOL; DNA; FEMALE; HEPATOCYTES; HUMANS; INFANT; INFANT, NEWBORN; LIVER DISEASES; MALE; METABOLIC DISEASES; PORTAL SYSTEM; TISSUE DONORS;

EID: 62549114070     PISSN: 09636897     EISSN: None     Source Type: Journal    
DOI: 10.3727/096368908787648083     Document Type: Article

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