Hereditary haemochromatosis;Hereditäre hämochromatose

Internist

Volumn 44, Issue 2, 2003, Pages 191-207

  Niederau, C ^a  

^a NONE

Author keywords

Diabetes mellitus; Ferritin; Haemochromatosis; Iron metabolism; Liver cirrhosis; Transferrin

Indexed keywords

CARRIER PROTEIN; DEFEROXAMINE; FERRITIN; FERROPORTIN 1; IRON; TRANSFERRIN; TRANSFERRIN RECEPTOR; UNCLASSIFIED DRUG;

ARTHROPATHY; AUTOSOMAL DOMINANT INHERITANCE; CARDIOMYOPATHY; CHROMOSOME 2Q; CHROMOSOME 7Q; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; DIABETES MELLITUS; DIAGNOSTIC PROCEDURE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; EARLY DIAGNOSIS; ENDOCRINE GLAND; GENE; GENE LOCATION; GENETIC DISORDER; GENOTYPE PHENOTYPE CORRELATION; HEMOCHROMATOSIS; HEPATITIS C; HETEROZYGOTE; HFE GENE; HUMAN; HYPOGONADISM; INSULIN RESISTANCE; INTESTINE ABSORPTION; IRON ABSORPTION; IRON OVERLOAD; IRON STORAGE; JUVENILE; LIVER; LIVER BIOPSY; LIVER CIRRHOSIS; LIVER DISEASE; LIVER TUMOR; MACROPHAGE; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; ORGAN INJURY; PANCREAS; PATHOGENESIS; PATHOLOGY; PATIENT CARE; PHLEBOTOMY; POINT MUTATION; PORPHYRIA; PROGNOSIS; PROTEIN BLOOD LEVEL; SCREENING TEST; SHORT SURVEY;

EID: 0037328095     PISSN: 00209554     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00108-002-0838-8     Document Type: Short Survey

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