Mieli-Vergani G. Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease. HEPATOLOGY
An association between Type 2 diabetes and α1-antitrypsin deficiency
✍ Scribed by C. S. Sandström; B. Ohlsson; O. Melander; U. Westin; R. Mahadeva; S. Janciauskiene
- Book ID
- 110925564
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 125 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0742-3071
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The phenotypes of alpha-1-antitrypsin have been analyzed by isoelectric focusing on polyacrylamide gels in 232 healthy Japanese blood donors and in 240 Japanese patients with chronic liver diseases: 69 with chronic active hepatitis, 122 with liver cirrhosis, 41 with hepatocellular carcinoma and 8 wi
Primary hemochromatosis is a genetically determined autosomal recessive disorder characterized by the excessive accumulation of body iron, most of which is deposited in the parenchymal cells of various organs. a,-Antitrypsin deficiency is characterized among others by defective secretion of a,-anti
synthesized in the liver and is regulated by a gene located Genetic hemochromatosis and a 1 -antitrypsin (AAT) on chromosome 14 for which several alleles have been dedeficiency are frequent in white populations. Conflictscribed. The most common allele, PiM, is associated with an ing data on the asso