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Journal Abstract Search

111 related items for PubMed ID: 10572206

  • 1. Protease inhibitor phenotype BsaskatoonM is not associated with emphysema - a 20-year follow-up study.
    Jokic R, Fisher KL, Cockcroft DW.
    Can Respir J; 1999; 6(5):407-11. PubMed ID: 10572206
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  • 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.
    McDonagh DJ, Nathan SP, Knudson RJ, Lebowitz MD.
    J Clin Invest; 1979 Feb; 63(2):299-309. PubMed ID: 311786
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  • 4. Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk.
    DeMeo DL, Silverman EK.
    Thorax; 2004 Mar; 59(3):259-64. PubMed ID: 14985567
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  • 7. Alpha 1-antitrypsin deficiency: the radiological features of pulmonary emphysema in subjects of Pi type Z and Pi type SZ: a survey by the British Thoracic Association.
    Gishen P, Saunders AJ, Tobin MJ, Hutchison DC.
    Clin Radiol; 1982 Jul; 33(4):371-7. PubMed ID: 6979454
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  • 8. Emphysema due to alpha-antitrypsin deficiency: familial study of the YBARCELONA variant.
    Miravitlles M, Vilà S, Jardí R, de la Roza C, Rodríguez-Frías F, Vidal R.
    Chest; 2003 Jul; 124(1):404-6. PubMed ID: 12853554
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  • 9. A new anodal alpha 1-antitrypsin variant associated with emphysema: Pi Bsaskatoon.
    Horne SL, Tennent RK, Cockcroft DW.
    Am Rev Respir Dis; 1982 May; 125(5):594-600. PubMed ID: 6979277
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  • 10. Longitudinal decline of diffusing capacity of the lung for carbon monoxide in community subjects with the PiMZ alpha1-antitrypsin phenotype.
    Silva GE, Guerra S, Keim S, Barbee RA, Sherrill DL.
    Chest; 2008 May; 133(5):1095-100. PubMed ID: 18263681
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  • 11. Emphysema of early onset associated with a complete deficiency of alpha-1-antitrypsin (null homozygotes).
    Cox DW, Levison H.
    Am Rev Respir Dis; 1988 Feb; 137(2):371-5. PubMed ID: 3257661
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  • 15. Alpha-1 antitrypsin Null mutations and severity of emphysema.
    Fregonese L, Stolk J, Frants RR, Veldhuisen B.
    Respir Med; 2008 Jun; 102(6):876-84. PubMed ID: 18353624
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  • 16. [Analysis of alpha-1-antitrypsin phenotypes and genotypes in patients with early-onset pulmonary emphysema].
    Dwomiczak S, Ziora D, Konofalski L, Szalaty M, Kowalska A, Kozielski J.
    Pneumonol Alergol Pol; 2005 Jun; 73(1):12-7. PubMed ID: 16539178
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  • 18. Family study of alpha 1-antitrypsin deficiency: effects of cigarette smoking, measured genotype, and their interaction on pulmonary function and biochemical traits.
    Silverman EK, Province MA, Campbell EJ, Pierce JA, Rao DC.
    Genet Epidemiol; 1992 Jun; 9(5):317-31. PubMed ID: 1427021
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  • 19. Alpha-1-antitrypsin deficiency in a large sibship.
    Apprill M, North ML, Mirhom R, Weitzenblum E.
    Respiration; 1990 Jun; 57(5):310-2. PubMed ID: 2284507
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  • 20. Absence of alpha-1-antitrypsin (Pi Null Bellingham) and the early onset of emphysema.
    Cook L, Janus ED, Brenton S, Tai E, Burdon J.
    Aust N Z J Med; 1994 Jun; 24(3):263-9. PubMed ID: 7980208
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