Hereditary hemochromatosis, alpha-1-antitrypsin deficiency and Wilson's disease. Pathogenesis, clinical findings and pathways to diagnosis;Hereditäre hämochromatose, alpha-1-antitrypsin-mangel und morbus Wilson. Pathogenese, klinik und wege zur diagnose

Pathologe

Volumn 29, Issue 1, 2008, Pages 73-83

  Zhou, H ^a   Fischer, H P ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

Alpha 1 antitrypsin deficiency; Hereditary hemochromatosis; Liver biopsy; Wilson's disease

Indexed keywords

ALPHA 1 ANTITRYPSIN DEFICIENCY; ARTICLE; BILE DUCT ATRESIA; CHRONIC HEPATITIS; DISEASE ASSOCIATION; GENE MUTATION; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; LIVER BIOPSY; LIVER DISEASE; SIDEROSIS; WILSON DISEASE; ZYGOSITY;

ADENOSINE TRIPHOSPHATASES; ADULT; ALPHA 1-ANTITRYPSIN DEFICIENCY; CATION TRANSPORT PROTEINS; CHILD; COPPER; DIAGNOSIS, DIFFERENTIAL; HEMOCHROMATOSIS; HEPATITIS; HEPATOLENTICULAR DEGENERATION; HETEROZYGOTE DETECTION; HUMANS; LIVER DISEASES; MUTATION; PROGNOSIS; YOUNG ADULT;

EID: 39149102116     PISSN: 01728113     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00292-007-0954-2     Document Type: Article

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