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PUBMED FOR HANDHELDS

Journal Abstract Search


191 related items for PubMed ID: 2284507

  • 41. Coagulation-fibrinolytic inhibitors on familial cases of alpha 1-antitrypsin deficiency.
    Hasegawa H, Nagata H, Irie T, Kawakami Y, Murao M.
    Nihon Ketsueki Gakkai Zasshi; 1982 Jul; 45(4):800-5. PubMed ID: 6982579
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  • 42. [Pulmonary emphysema and liver changes in alpha 1-antitrypsin deficiency. Study of a family].
    Lindskov J, Reinicke V, Clausen PP.
    Ugeskr Laeger; 1978 Jun 26; 140(26):1551-5. PubMed ID: 308269
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  • 43. 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 26; 133(5):1095-100. PubMed ID: 18263681
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  • 44. The prevalence of bronchiectasis in patients with alpha-1 antitrypsin deficiency: initial report of EARCO.
    Stockley RA, Pye A, De Soyza J, Turner AM, Miravitlles M, EARCO study investigators.
    Orphanet J Rare Dis; 2023 Aug 12; 18(1):243. PubMed ID: 37573351
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  • 45. [Chronic progressive pulmonary emphysema associated with homozygous alpha 1-antitrypsin deficiency (author's transl)].
    Thiel H, Oellig WP, Rasche B.
    Prax Klin Pneumol; 1981 Jan 12; 35(1):23-8. PubMed ID: 6970928
    [No Abstract] [Full Text] [Related]

  • 46. A matched-pair study of the leukocyte elastase-like activity in normal persons and in emphysematous patients with and without alpha 1-antitrypsin deficiency.
    Kramps JA, Bakker W, Dijkman JH.
    Am Rev Respir Dis; 1980 Feb 12; 121(2):253-61. PubMed ID: 6965829
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  • 48. Alpha 1-antitrypsin deficiency caused by the alpha 1-antitrypsin Nullmattawa gene. An insertion mutation rendering the alpha 1-antitrypsin gene incapable of producing alpha 1-antitrypsin.
    Curiel D, Brantly M, Curiel E, Stier L, Crystal RG.
    J Clin Invest; 1989 Apr 12; 83(4):1144-52. PubMed ID: 2539391
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  • 49. Emphysema associated with complete absence of alpha 1- antitrypsin in serum and the homozygous inheritance [corrected] of a stop codon in an alpha 1-antitrypsin-coding exon.
    Satoh K, Nukiwa T, Brantly M, Garver RI, Hofker M, Courtney M, Crystal RG.
    Am J Hum Genet; 1988 Jan 12; 42(1):77-83. PubMed ID: 3257351
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  • 50. Biochemical intermediates in alpha 1-antitrypsin deficiency: residual family resemblance for total alpha 1-antitrypsin, oxidized alpha 1-antitrypsin, and immunoglobulin E after adjustment for the effect of the Pi locus.
    Silverman EK, Province MA, Campbell EJ, Pierce JA, Rao DC.
    Genet Epidemiol; 1990 Jan 12; 7(2):137-49. PubMed ID: 2338230
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  • 53. Small airway evaluation in three subjects with alpha-1 antitrypsin deficiency without diagnosed lung disease.
    Ferrari da Cruz T, Rufino R, Lopes A, Henrique Costa C.
    BMJ Case Rep; 2021 Mar 30; 14(3):. PubMed ID: 33785603
    [Abstract] [Full Text] [Related]

  • 54. [Alpha 1-antitrypsin phenotypes and their role in medical diagnosis].
    Piłacik B.
    Med Pr; 1987 Mar 30; 38(5):376-83. PubMed ID: 3328031
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  • 56. 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 Mar 30; 9(5):317-31. PubMed ID: 1427021
    [Abstract] [Full Text] [Related]

  • 57. [Genetically-induced deficiency of alpha 1-antitrypsin and diseases of the lung--current assessment and perspectives].
    Stobernack A, Theise H, Tischer H, Correns A.
    Z Arztl Fortbild (Jena); 1990 Mar 30; 84(22):1144-8. PubMed ID: 2087809
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