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317 related items for PubMed ID: 3289385

  • 1. Molecular basis of alpha-1-antitrypsin deficiency.
    Brantly M, Nukiwa T, Crystal RG.
    Am J Med; 1988 Jun 24; 84(6A):13-31. PubMed ID: 3289385
    [Abstract] [Full Text] [Related]

  • 2. Alpha-1 Antitrypsin Deficiency: Current Perspective from Genetics to Diagnosis and Therapeutic Approaches.
    Santangelo S, Scarlata S, Poeta ML, Bialas AJ, Paone G, Incalzi RA.
    Curr Med Chem; 2017 Jun 24; 24(1):65-90. PubMed ID: 27855621
    [Abstract] [Full Text] [Related]

  • 3. Frequency of Rare Alpha-1 Antitrypsin Variants in Polish Patients with Chronic Respiratory Disorders.
    Duk K, Zdral A, Szumna B, Roży A, Chorostowska-Wynimko J.
    Adv Exp Med Biol; 2016 Jun 24; 910():47-53. PubMed ID: 26987331
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  • 5. A rare variant of α 1 antitrypsin mutations detected in Vietnamese children with liver disease.
    Hoàng TH, Phạm TN, Nguyễn GK, Lê QH.
    Ann Clin Biochem; 2013 Jul 24; 50(Pt 4):339-44. PubMed ID: 23766346
    [Abstract] [Full Text] [Related]

  • 6. NullCanada: A novel α1-antitrypsin allele with in cis variants Glu366Lys and Ile100Asn.
    Chen S, DeMarco ML, Estey MP, Kyle B, Parker ML, Agbor TA, Kawada P, Speevak M, Nelson TN, Mattman A.
    Clin Biochem; 2020 May 24; 79():23-27. PubMed ID: 32087139
    [Abstract] [Full Text] [Related]

  • 7. Alpha-1 antitrypsin deficiency: a conformational disease associated with lung and liver manifestations.
    Greene CM, Miller SD, Carroll T, McLean C, O'Mahony M, Lawless MW, O'Neill SJ, Taggart CC, McElvaney NG.
    J Inherit Metab Dis; 2008 Feb 24; 31(1):21-34. PubMed ID: 18193338
    [Abstract] [Full Text] [Related]

  • 8. [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 Feb 24; 73(1):12-7. PubMed ID: 16539178
    [Abstract] [Full Text] [Related]

  • 9. Well-Known and Less Well-Known Functions of Alpha-1 Antitrypsin. Its Role in Chronic Obstructive Pulmonary Disease and Other Disease Developments.
    Janciauskiene S, Welte T.
    Ann Am Thorac Soc; 2016 Aug 24; 13 Suppl 4():S280-8. PubMed ID: 27564662
    [Abstract] [Full Text] [Related]

  • 10. Deletion of Serpina1a, a murine α1-antitrypsin ortholog, results in embryonic lethality.
    Wang D, Wang W, Dawkins P, Paterson T, Kalsheker N, Sallenave JM, Houghton AM.
    Exp Lung Res; 2011 Jun 24; 37(5):291-300. PubMed ID: 21574874
    [Abstract] [Full Text] [Related]

  • 11. 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 24; 83(4):1144-52. PubMed ID: 2539391
    [Abstract] [Full Text] [Related]

  • 12. Molecular basis of alpha 1-antitrypsin deficiency and emphysema associated with the alpha 1-antitrypsin Mmineral springs allele.
    Curiel DT, Vogelmeier C, Hubbard RC, Stier LE, Crystal RG.
    Mol Cell Biol; 1990 Jan 24; 10(1):47-56. PubMed ID: 1967187
    [Abstract] [Full Text] [Related]

  • 13. Alpha-1-antitrypsin deficiency: current concepts.
    Mulgrew AT, Taggart CC, McElvaney NG.
    Lung; 2007 Jan 24; 185(4):191-201. PubMed ID: 17562108
    [Abstract] [Full Text] [Related]

  • 14. Secretory leukocyte proteinase inhibitor, alpha-1-antitrypsin deficiency and emphysema: Preliminary study, speculation and an hypothesis.
    Ayad MS, Knight KR, Burdon JG, Brenton S.
    Respirology; 2003 Jun 24; 8(2):175-80. PubMed ID: 12753532
    [Abstract] [Full Text] [Related]

  • 15. The alpha 1-antitrypsin gene and its deficiency states.
    Crystal RG.
    Trends Genet; 1989 Dec 24; 5(12):411-7. PubMed ID: 2696185
    [Abstract] [Full Text] [Related]

  • 16. Alpha 1-antitrypsin deficiency: an overview.
    van Steenbergen W.
    Acta Clin Belg; 1993 Dec 24; 48(3):171-89. PubMed ID: 8396299
    [Abstract] [Full Text] [Related]

  • 17. Function of a rare variant of alpha-1-antitrypsin, phenotype P(i) EFranklin S, a poor inhibitor of human neutrophil elastase.
    Cook L, Knight KR, Burdon JG, Brenton S, Hunt JM.
    Res Exp Med (Berl); 1997 Dec 24; 196(6):355-62. PubMed ID: 9089884
    [Abstract] [Full Text] [Related]

  • 18. The role of augmentation therapy in alpha-1 antitrypsin deficiency.
    Kueppers F.
    Curr Med Res Opin; 2011 Mar 24; 27(3):579-88. PubMed ID: 21226542
    [Abstract] [Full Text] [Related]

  • 19. Gene targeted therapeutics for liver disease in alpha-1 antitrypsin deficiency.
    McLean C, Greene CM, McElvaney NG.
    Biologics; 2009 Mar 24; 3():63-75. PubMed ID: 19707397
    [Abstract] [Full Text] [Related]

  • 20. 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 Mar 24; 52(4):223-32. PubMed ID: 11713419
    [Abstract] [Full Text] [Related]

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