BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 3874784)

  • 21. Z and S mutations of the alpha1-antitrypsin gene and the risk of chronic obstructive pulmonary disease.
    Sandford AJ; Weir TD; Spinelli JJ; Paré PD
    Am J Respir Cell Mol Biol; 1999 Feb; 20(2):287-91. PubMed ID: 9922220
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Physiological studies in a large sibship with antitrypsin deficiency.
    Duncan PE; Griffin JP
    Br J Dis Chest; 1975 Apr; 69(2):107-17. PubMed ID: 49190
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Alpha-1-antitrypsin deficiency. Phenotype study of 60 members of the same family].
    Saugier B; Chapuis-Cellier C; Emonot A; Vittoz P; Galy P
    Sem Hop; 1977 Feb; 53(7):413-6. PubMed ID: 190685
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetics of chronic obstructive pulmonary disease.
    Silverman EK
    Novartis Found Symp; 2001; 234():45-58; discussion 58-64. PubMed ID: 11199103
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Clinical aspects, results of diagnostic pulmonary function tests and biochemical parameters in children with homozygote alpha-1-antitrypsin deficiency].
    Paul K; Heck B; Schulz V; Ebert W; Trefz G; Feist D
    Pneumologie; 1990 Oct; 44(10):1217-9. PubMed ID: 2281074
    [TBL] [Abstract][Full Text] [Related]  

  • 26. PI SZ phenotype in chronic obstructive pulmonary disease.
    Alvarez-Granda L; Cabero-Perez MJ; Bustamante-Ruiz A; Gonzalez-Lamuño D; Delgado-Rodriguez M; García-Fuentes M
    Thorax; 1997 Jul; 52(7):659-61. PubMed ID: 9246142
    [TBL] [Abstract][Full Text] [Related]  

  • 27. SZ alpha-1 antitrypsin deficiency and pulmonary disease: more like MZ, not like ZZ.
    Franciosi AN; Carroll TP; McElvaney NG
    Thorax; 2021 Mar; 76(3):298-301. PubMed ID: 32917839
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The prevalence of alpha-1 antitrypsin deficiency among patients found to have airflow obstruction.
    Rahaghi FF; Sandhaus RA; Brantly ML; Rouhani F; Campos MA; Strange C; Hogarth DK; Eden E; Stocks JM; Krowka MJ; Stoller JK
    COPD; 2012 Aug; 9(4):352-8. PubMed ID: 22506682
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A family study of the variability of pulmonary function in alpha 1-antitrypsin deficiency. Quantitative phenotypes.
    Silverman EK; Province MA; Rao DC; Pierce JA; Campbell EJ
    Am Rev Respir Dis; 1990 Nov; 142(5):1015-21. PubMed ID: 2240821
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Alpha 1-antitrypsin deficiency and the flaccid lung syndrome. The heterozygote controversy.
    Klasen EC; Biemond I; Laros CD
    Clin Genet; 1986 Mar; 29(3):211-5. PubMed ID: 3486059
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 121(3):507-12. PubMed ID: 6968167
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Heterozygous alpha 1-antitrypsin deficiency: a longitudinal lung function study.
    de Hamel FA; Carrell RW
    N Z Med J; 1981 Dec; 94(697):407-10. PubMed ID: 6977750
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Intermediate alpha1-antitrypsin deficiency and chronic obstructive pulmonary disease in Yugoslavia.
    Kozarevic D; Laban M; Budimir M; Vojvodic N; Roberts A; Gordon T; McGee DL
    Am Rev Respir Dis; 1978 Jun; 117(6):1039-43. PubMed ID: 307352
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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; 68(17):857-63. PubMed ID: 2214609
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Collaborative study to assess risk of lung disease in Pi MZ phenotype subjects.
    Bruce RM; Cohen BH; Diamond EL; Fallat RJ; Knudson RJ; Lebowitz MD; Mittman C; Patterson CD; Tockman MS
    Am Rev Respir Dis; 1984 Sep; 130(3):386-90. PubMed ID: 6332562
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Clinical phenotypes of Italian and Spanish patients with α1-antitrypsin deficiency.
    Piras B; Ferrarotti I; Lara B; Martinez MT; Bustamante A; Ottaviani S; Pirina P; Luisetti M; Miravitlles M
    Eur Respir J; 2013 Jul; 42(1):54-64. PubMed ID: 23222880
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Determinants of chronic obstructive pulmonary disease in patients with intermediate levels of alpha-antitrypsin.
    Klayton R; Fallat R; Cohen AB
    Am Rev Respir Dis; 1975 Jul; 112(1):71-5. PubMed ID: 238443
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Familial predisposition to chronic obstructive pulmonary disease].
    Rowińska-Zakrzewska E
    Pneumonol Alergol Pol; 2009; 77(4):407-10. PubMed ID: 19722147
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Alpha-1 Antitrypsin Deficiency in COPD Patients: A Cross-Sectional Study.
    Sorroche PB; Fernández Acquier M; López Jove O; Giugno E; Pace S; Livellara B; Legal S; Oyhamburu J; Saez MS
    Arch Bronconeumol; 2015 Nov; 51(11):539-43. PubMed ID: 25800328
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Alpha-1 antitrypsin deficiency, SZ phenotype: a rare type of a rare disease. Case report.
    Nebunoiu AM; Deleanu OC; Rohan I; Mihălţan F; Chorostowska-Wynimko J; Ulmeanu R
    Pneumologia; 2014; 63(4):218-23. PubMed ID: 25665366
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.