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Proceedings of the Royal Society of Medicine logoLink to Proceedings of the Royal Society of Medicine
. 1976 Feb;69(2):130–131. doi: 10.1177/003591577606900220

Homozygous and heterozygous alpha-1-antitrypsin deficiency: prevalence in pulmonary emphysema.

D C Hutchison
PMCID: PMC1864449  PMID: 1083529

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Cole R. B., Nevin N. C., Blundell G. Proceedings: The effect of variation in alpha 1-antitrypsin phenotype upon the incidence of respiratory illness in a working population. Clin Sci Mol Med. 1974 Nov;47(5):26P–27P. doi: 10.1042/cs047026pb. [DOI] [PubMed] [Google Scholar]
  2. Cook P. J. Genetic aspects of the Pi system. Postgrad Med J. 1974 Jun;50(584):362–364. doi: 10.1136/pgmj.50.584.362. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cooper D. M., Hoeppner V., Cox D., Zamel N., Bryan A. C., Levison H. Lung function in alpha1-antitrypsin heterozygotes (Pi type MZ). Am Rev Respir Dis. 1974 Dec;110(6):708–715. doi: 10.1164/arrd.1974.110.6P1.708. [DOI] [PubMed] [Google Scholar]
  4. Hutchison D. C., Cook P. J., Barter C. E., Harris H., Hugh-Jones P. Pulmonary emphysema and alpha 1-antitrypsin deficiency. Br Med J. 1971 Mar 27;1(5751):689–694. doi: 10.1136/bmj.1.5751.689. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Jones M. C., Thomas G. O. Alpha antitrypsin deficiency and pulmonary emphysema. Thorax. 1971 Nov;26(6):652–662. doi: 10.1136/thx.26.6.652. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. KUEPPERS F., BRISCOE W. A., BEARN A. G. HEREDITARY DEFICIENCY OF SERUM ALPHA-L-ANTITRYPSIN. Science. 1964 Dec 25;146(3652):1678–1679. doi: 10.1126/science.146.3652.1678. [DOI] [PubMed] [Google Scholar]
  7. Kellermann G., Walter H. Investigations on the population genetics of the alpha-1-antitrypsin polymorphism. Humangenetik. 1970 Sep 17;10(2):145–150. doi: 10.1007/BF00295513. [DOI] [PubMed] [Google Scholar]
  8. Kueppers F., Dönhardt A. Obstructive lung disease in heterozygotes for alpha-1 antitrypsin deficiency. Ann Intern Med. 1974 Feb;80(2):209–212. doi: 10.7326/0003-4819-80-2-209. [DOI] [PubMed] [Google Scholar]
  9. Kueppers F., Fallat R., Larson R. K. Obstructive lung disease and alpha-1-antitrypsin deficiency gene heterozygosity. Science. 1969 Aug 29;165(3896):899–901. doi: 10.1126/science.165.3896.899. [DOI] [PubMed] [Google Scholar]
  10. Lieberman J., Mittman C., Schneider A. S. Screening for homozygous and heterozygous alpha 1-antitrypsin deficiency. Protein electrophoresis on cellulose acetate membranes. JAMA. 1969 Dec 15;210(11):2055–2060. [PubMed] [Google Scholar]
  11. Talamo R. C., Allen J. D., Kahan M. G., Auste K. F. Hereditary alpha-1-antitrypsin deficiency. N Engl J Med. 1968 Feb 15;278(7):345–351. doi: 10.1056/NEJM196802152780701. [DOI] [PubMed] [Google Scholar]
  12. Webb D. R., Hyde R. W., Schwartz R. H., Hall W. J., Condemi J. J., Townes P. L. Serum alpha 1-antitrypsin variants. Prevalence and clinical spirometry. Am Rev Respir Dis. 1973 Oct;108(4):918–925. doi: 10.1164/arrd.1973.108.4.918. [DOI] [PubMed] [Google Scholar]

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