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Journal Abstract Search

219 related items for PubMed ID: 2240821

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  • 2. 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; 9(5):317-31. PubMed ID: 1427021
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  • 6. Clinical features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group.
    Turino GM, Barker AF, Brantly ML, Cohen AB, Connelly RP, Crystal RG, Eden E, Schluchter MD, Stoller JK.
    Am J Respir Crit Care Med; 1996 Dec; 154(6 Pt 1):1718-25. PubMed ID: 8970361
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  • 7. Highly variable clinical course in severe alpha 1-antitrypsin deficiency--use of polymerase chain reaction for the detection of rare deficiency alleles.
    Poller W, Faber JP, Olek K.
    Klin Wochenschr; 1990 Sep 03; 68(17):857-63. PubMed ID: 2214609
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  • 10. Genetic epidemiology of severe, early-onset chronic obstructive pulmonary disease. Risk to relatives for airflow obstruction and chronic bronchitis.
    Silverman EK, Chapman HA, Drazen JM, Weiss ST, Rosner B, Campbell EJ, O'DONNELL WJ, Reilly JJ, Ginns L, Mentzer S, Wain J, Speizer FE.
    Am J Respir Crit Care Med; 1998 Jun 03; 157(6 Pt 1):1770-8. PubMed ID: 9620904
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  • 12. Interrelationships between serum chemotactic factor inactivator, alpha 1-antitrypsin deficiency, and chronic obstructive lung disease.
    Lam S, Chan-Yeung M, Abboud R, Kreutzer D.
    Am Rev Respir Dis; 1980 Mar 03; 121(3):507-12. PubMed ID: 6968167
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  • 13. Molecular characterisation of the defective alpha 1-antitrypsin alleles PI Mwurzburg (Pro369Ser), Mheerlen (Pro369Leu), and Q0lisbon (Thr68Ile).
    Poller W, Merklein F, Schneider-Rasp S, Haack A, Fechner H, Wang H, Anagnostopoulos I, Weidinger S.
    Eur J Hum Genet; 1999 Apr 03; 7(3):321-31. PubMed ID: 10234508
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  • 16. Heritability of lung function in severe alpha-1 antitrypsin deficiency.
    DeMeo DL, Campbell EJ, Brantly ML, Barker AF, Eden E, McElvaney NG, Rennard SI, Stocks JM, Stoller JK, Strange C, Turino G, Sandhaus RA, Silverman EK.
    Hum Hered; 2009 Apr 03; 67(1):38-45. PubMed ID: 18931508
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  • 17. Heterozygous alpha-1-antitrypsin deficiency and respiratory function in children.
    Vance JC, Hall WJ, Schwartz RH, Hyde RW, Roghmann KJ, Mudholkar GC.
    Pediatrics; 1977 Sep 03; 60(3):263-72. PubMed ID: 302433
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  • 18. Linkage analysis of alpha 1-antitrypsin deficiency: lessons for complex diseases.
    Silverman EK, Mosley JD, Rao DC, Palmer LJ, Province MA, Elston RC, Weiss ST, Campbell EJ.
    Hum Hered; 2001 Sep 03; 52(4):223-32. PubMed ID: 11713419
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