A 30-Year Perspective on α1-Antitrypsin Deficiency
- 1 December 1996
- Vol. 110 (6) , 237S-242S
- https://doi.org/10.1378/chest.110.6_supplement.237s
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- The putative role of alpha-1-antitrypsin in the disaggregation of amyloid lambda fibrilsJournal of Internal Medicine, 1995
- In VitroAmyloid Fibril Formation from α1-AntitrypsinBiological Chemistry Hoppe-Seyler, 1995
- The interaction of hydrophobic bile acids with the α1‐proteinase inhibitorFEBS Letters, 1994
- Mis-sense mutation of α1-antichymotrypsin gene associated with chronic lung diseaseThe Lancet, 1992
- Identification of hydrophobic fragments of α1‐antitrypsin and Cl protease inhibitor in human bile, plasma and spleenFEBS Letters, 1992
- α1‐antitrypsin deficiency and liver disease: Clinical presentation, diagnosis and treatmentJournal of Inherited Metabolic Disease, 1991
- Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy.Journal of Clinical Investigation, 1990
- Alpha-1-antitrypsin deficiency and panniculitis: Perspectives on disease relationship and replacement therapyPublished by Elsevier ,1988
- Prospective study of children with α1-antitrypsin deficiency: Eight-year-old follow-upThe Journal of Pediatrics, 1984
- Amino acid substitution Glu→Lys in α1‐antitrypsin PiZFEBS Letters, 1976