Heterozygous FZ alpha 1 antitrypsin deficiency associated with severe emphysema and hepatic disease: case report and family study.-Reference-Cited by-同舟云学术

Heterozygous FZ alpha 1 antitrypsin deficiency associated with severe emphysema and hepatic disease: case report and family study.

Published:1989-09-01 Issue:9 Volume:44 Page:758-759
ISSN:0040-6376
Container-title:Thorax
language:en
Short-container-title:Thorax

Author:

Kelly C P,Tyrrell D N,McDonald G S,Whitehouse D B,Prichard J S

Publisher

BMJ

Subject

Pulmonary and Respiratory Medicine

Reference10 articles.

1. Alpha-l-antitrypsin and the pathogenesis of emphysema;RA, I.Stockley;Lung,1987

2. Cirrhosis associated with alpha-one antitrypsin deficiency: a previously unrecognised inherited disorder;Sharp, H.L.; Bridges, R.A.; Krivit, W.; Freier, E.F.;J Lab Clin Med

3. Alpha-one antitrypsin deficiency: clinical and physiological features in heterozygotes of Pi type SZ;Hutchison, D.C.S.; Tobin, M.J.; Cook, P.J.L.;Br J Dis Chest,1983

4. Serum prealbumin: polymorphism in man;Fagerhol, M.K.; Braemd, M.;Science,1965

5. Isthe PiFalleleofalpha-one anti-trypsin associated with pulmonary disease?;BeckmanG, StjernbergN; A, Eklund;Clin Genet,1984

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