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Editorial
. 2020 Oct;63(4):403-404.
doi: 10.1165/rcmb.2020-0243ED.

Bench to Bedside and Back: The Evolving Story of Alpha-1 Antitrypsin Deficiency

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Editorial

Bench to Bedside and Back: The Evolving Story of Alpha-1 Antitrypsin Deficiency

Kenneth R Chapman. Am J Respir Cell Mol Biol. 2020 Oct.
No abstract available

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References

    1. Laurell CB, Eriksson S. The electrophoretic alpha1-globullin pattern of serum in alpha1-antitrypsin deficiency. Scand J Clin Lab Invest. 1963;115:132–140.
    1. Wewers MD, Casolaro MA, Sellers SE, Swayze SC, McPhaul KM, Wittes JT, et al. Replacement therapy for alpha 1-antitrypsin deficiency associated with emphysema. N Engl J Med. 1987;316:1055–1062. - PubMed
    1. Vreim CE, Wu M, Crystal RG, Buist AS, Burrows B, Cohen AB, et al. Survival and FEV1 decline in individuals with severe deficiency of α1-antitrypsin. Am J Respir Crit Care Med. 1998;158:49–59. - PubMed
    1. Chapman KR, Stockley RA, Dawkins C, Wilkes MM, Navickis RJ. Augmentation therapy for alpha1 antitrypsin deficiency: a meta-analysis. COPD. 2009;6:177–184. - PubMed
    1. Chapman KR, Burdon JG, Piitulainen E, Sandhaus RA, Seersholm N, Stocks JM, et al. RAPID Trial Study Group. Intravenous augmentation treatment and lung density in severe α1 antitrypsin deficiency (RAPID): a randomised, double-blind, placebo-controlled trial. Lancet. 2015;386:360–368. - PubMed

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