Literature DB >> 4987089

The pattern of inheritance of alpha 1 antitrypsin deficiency and associated pulmonary disease.

R H Richardson, C A Guenter, M H Welch, R M Hyde, J F Hammarsten.   

Abstract

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Year:  1969        PMID： 4987089     DOI： 10.1164/arrd.1969.100.5.619

Source DB:  PubMed          Journal:  Am Rev Respir Dis        ISSN： 0003-0805


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  4 in total

1.  Enzymes and emphysema.

Authors: 
Journal:  Br Med J       Date:  1973-01-06

2.  Assessment of alpha-1-antitrypsin deficiency heterozygosity as a risk factor in the etiology of emphysema. Physiological comparison of adult normal and heterozygous protease inhibitor phenotype subjects from a random population.

Authors:  D J McDonagh; S P Nathan; R J Knudson; M D Lebowitz
Journal:  J Clin Invest       Date:  1979-02       Impact factor: 14.808

3.  An epidemiological approach to chronic obstructive pulmonary disease and alpha antitrypsin in hospital patients: a tri-racial study.

Authors:  J F Hammarsten; L Henderson; C A Guenter; S Ferguson; M H Welch
Journal:  Trans Am Clin Climatol Assoc       Date:  1971

Review 4.  Relation of alpha-1-antitrypsin phenotype to the performance of pulmonary function tests and to the prevalence of respiratory illness in a working population.

Authors:  R B Cole; N C Nevin; G Blundell; J D Merrett; J R McDonald; W P Johnston
Journal:  Thorax       Date:  1976-04       Impact factor: 9.139
  4 in total

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