These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


588 related items for PubMed ID: 18931508

  • 1. 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; 67(1):38-45. PubMed ID: 18931508
    [Abstract] [Full Text] [Related]

  • 2. Screening for alpha1-antitrypsin deficiency in Lithuanian patients with COPD.
    Sitkauskiene B, Serapinas D, Blanco I, Fernández-Bustillo E, Janciauskiene S, Sakalauskas R.
    Respir Med; 2008 Nov; 102(11):1654-8. PubMed ID: 18722101
    [Abstract] [Full Text] [Related]

  • 3. A review of alpha-1 antitrypsin deficiency.
    Ranes J, Stoller JK.
    Semin Respir Crit Care Med; 2005 Apr; 26(2):154-66. PubMed ID: 16088434
    [Abstract] [Full Text] [Related]

  • 4. Relation of functional characteristics and serum alpha-1-antitrypsin (AAT) concentration in patients with PiMM phenotype and chronic obstructive pulmonary disease (COPD).
    Zarić B, Stojčević J, Andrijević L, Andrijević I, Kuruc V, Veselinović I, Salatić I.
    Eur J Intern Med; 2011 Dec; 22(6):603-6. PubMed ID: 22075288
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. IL10 polymorphisms are associated with airflow obstruction in severe alpha1-antitrypsin deficiency.
    Demeo DL, Campbell EJ, Barker AF, Brantly ML, Eden E, McElvaney NG, Rennard SI, Sandhaus RA, Stocks JM, Stoller JK, Strange C, Turino G, Silverman EK.
    Am J Respir Cell Mol Biol; 2008 Jan; 38(1):114-20. PubMed ID: 17690329
    [Abstract] [Full Text] [Related]

  • 8. 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 Jan; 9(5):317-31. PubMed ID: 1427021
    [Abstract] [Full Text] [Related]

  • 9. Plasma levels of alpha1-antichymotrypsin and secretory leukocyte proteinase inhibitor in healthy and chronic obstructive pulmonary disease (COPD) subjects with and without severe alpha1-antitrypsin deficiency.
    Hollander C, Westin U, Wallmark A, Piitulainen E, Sveger T, Janciauskiene SM.
    BMC Pulm Med; 2007 Jan 29; 7():1. PubMed ID: 17261175
    [Abstract] [Full Text] [Related]

  • 10. Respiratory symptoms and lung function in 30-year-old individuals with alpha-1-antitrypsin deficiency.
    Bernspång E, Sveger T, Piitulainen E.
    Respir Med; 2007 Sep 29; 101(9):1971-6. PubMed ID: 17532199
    [Abstract] [Full Text] [Related]

  • 11. Decline in FEV1 in relation to incident chronic obstructive pulmonary disease in a cohort with respiratory symptoms.
    Lindberg A, Larsson LG, Rönmark E, Jonsson AC, Larsson K, Lundbäck B.
    COPD; 2007 Mar 29; 4(1):5-13. PubMed ID: 17364672
    [Abstract] [Full Text] [Related]

  • 12. Deficient alpha-1-antitrypsin phenotypes and persistent airflow limitation in severe asthma.
    van Veen IH, ten Brinke A, van der Linden AC, Rabe KF, Bel EH.
    Respir Med; 2006 Sep 29; 100(9):1534-9. PubMed ID: 16476537
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Health status and lung function in the Swedish alpha 1-antitrypsin deficient cohort, identified by neonatal screening, at the age of 37-40 years.
    Piitulainen E, Mostafavi B, Tanash HA.
    Int J Chron Obstruct Pulmon Dis; 2017 Sep 29; 12():495-500. PubMed ID: 28203073
    [Abstract] [Full Text] [Related]

  • 15. Alpha 1-antitrypsin deficiency: memorandum from a WHO meeting.
    Bull World Health Organ; 1997 Sep 29; 75(5):397-415. PubMed ID: 9447774
    [Abstract] [Full Text] [Related]

  • 16. The natural history of lung function after lung transplantation for α(1)-antitrypsin deficiency.
    Banga A, Gildea T, Rajeswaran J, Rokadia H, Blackstone EH, Stoller JK.
    Am J Respir Crit Care Med; 2014 Aug 01; 190(3):274-81. PubMed ID: 25003824
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic differences in alpha 1 antitrypsin-deficient sibling pairs may relate to genetic variation.
    Wood AM, Needham M, Simmonds MJ, Newby PR, Gough SC, Stockley RA.
    COPD; 2008 Dec 01; 5(6):353-9. PubMed ID: 19353349
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [The importance of the at risk COPD patients (Stage 0) and clinical differences].
    Kömüs N, Tertemiz KC, Sevinç C.
    Tuberk Toraks; 2008 Dec 01; 56(4):382-9. PubMed ID: 19123073
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 157(6 Pt 1):1770-8. PubMed ID: 9620904
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 30.