115 related articles for article (PubMed ID: 2034645)
1. [Genetic polymorphism of alpha 1-proteinase inhibitor in children and adolescents with tuberculosis and non-specific diseases of the lungs].
Pilipchuk VN; Blizniuk-Chodorovskaia OI; Slabchenko VG
Probl Tuberk; 1991; (2):5-7. PubMed ID: 2034645
[No Abstract] [Full Text] [Related]
2. [Homozygous alpha 1-antitrypsin deficiency. Lung changes in children and adolescents].
Paul K; Niggemann B
Monatsschr Kinderheilkd; 1993 May; 141(5):395-400. PubMed ID: 8326958
[TBL] [Abstract][Full Text] [Related]
3. alpha-1-Antitrypsin deficiency: associated diseases and their treatment.
Talamo RC
Prog Clin Biol Res; 1979; 34():265-70. PubMed ID: 316896
[No Abstract] [Full Text] [Related]
4. [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; 84(22):1144-8. PubMed ID: 2087809
[No Abstract] [Full Text] [Related]
5. The Pi polymorphism: genetic, biochemical, and clinical aspects of human alpha 1-antitrypsin.
Fagerhol MK; Cox DW
Adv Hum Genet; 1981; 11():1-62, 371-2. PubMed ID: 6168185
[No Abstract] [Full Text] [Related]
6. Three cases of alpha 1-antitrypsin deficiency: a review of diagnostic and therapeutic strategies.
Jenkins DW
Tex Med; 1992 Jan; 88(1):77-9. PubMed ID: 1557707
[TBL] [Abstract][Full Text] [Related]
7. [Laboratory procedures in the detection of deficiencies and the determination of alpha 1-antitrypsin phenotypes in the blood serum].
Piłacik B; Kowalczyk J
Med Pr; 1979; 30(3):207-12. PubMed ID: 314559
[TBL] [Abstract][Full Text] [Related]
8. [Obstructive pulmonary syndromes in children with alpha 1 antitrypsin deficiency. 3 cases].
Gerbeaux J; Grimfeld A; Gaultier C; Baculard A; Mensch B; Tournier G
Nouv Presse Med; 1975 Dec; 4(43):3045-50. PubMed ID: 1083504
[TBL] [Abstract][Full Text] [Related]
9. Independent mutations in the flanking sequence of the alpha-1-antitrypsin gene are associated with chronic obstructive airways disease.
Kalsheker NA; Watkins GL; Hill S; Morgan K; Stockley RA; Fick RB
Dis Markers; 1990; 8(3):151-7. PubMed ID: 1980238
[TBL] [Abstract][Full Text] [Related]
10. [Etiologic significance of hereditary deficiency of proteinase alpha1-inhibitor in the formation of respiratory diseases].
Gembitskaia TE; Monakhov NK; Ignat'ev VA; Aleĭnikova TD; Shavlovskiĭ MM
Ter Arkh; 1989; 61(3):88-91. PubMed ID: 2787064
[TBL] [Abstract][Full Text] [Related]
11. [Genetics of alpha 1-antitrypsin and chronic obstructive lung diseases].
Mirrakhimov MM; Ibraimov AI
Ter Arkh; 1977; 49(10):132-8. PubMed ID: 339390
[No Abstract] [Full Text] [Related]
12. Is the PiF allele of alpha 1-antitrypsin associated with pulmonary disease?
Beckman G; Stjernberg NL; Eklund A
Clin Genet; 1984 Jun; 25(6):491-5. PubMed ID: 6610506
[TBL] [Abstract][Full Text] [Related]
13. [Genetic research in tubercular pulmonology (a review of the literature)].
Pilipchuk VN; Slabchenko VG; Padalko IM
Lik Sprava; 1992 Jun; (6):25-8. PubMed ID: 1455824
[No Abstract] [Full Text] [Related]
14. [Pathologic phenotypes of alpha 1-protease inhibitor in patients with pulmonary tuberculosis].
Muminov TA; Medvedskiĭ SM; Talbaev TD; Il'chenko LA; Sharmanov AT
Probl Tuberk; 1991; (3):67-8. PubMed ID: 1714580
[No Abstract] [Full Text] [Related]
15. Genetic types of alpha-1-antitrypsin in Chinese patients with chronic obstructive pulmonary diseases.
Yin QL; Liang ZQ; Liang CC; Zhang ML; Mao J; Zhu YJ; Luo WC; Zheng WH
Proc Chin Acad Med Sci Peking Union Med Coll; 1986; 1(3):164-8. PubMed ID: 3501119
[No Abstract] [Full Text] [Related]
16. Clinical manifestations of alpha 1-antitrypsin deficiency.
Perlmutter DH
Gastroenterol Clin North Am; 1995 Mar; 24(1):27-43. PubMed ID: 7729860
[TBL] [Abstract][Full Text] [Related]
17. [DNA polymorphism of the alpha 2-macroglobulin gene in patients with chronic obstructive lung disease and serum alpha 2-macroglobulin deficiency].
Poller W; Barth J; Klobeck G; Ulmer W
Verh Dtsch Ges Inn Med; 1989; 95():7-12. PubMed ID: 2481372
[No Abstract] [Full Text] [Related]
18. Chronic obstructive pulmonary disease and alpha-1-antitrypsin (Pi) variation: a family study.
Benjamin JJ; Cohen BH; Ball WC; Levy DA; Menkes HA; Kreiss P
Birth Defects Orig Artic Ser; 1974; 10(4):212-6. PubMed ID: 4549777
[TBL] [Abstract][Full Text] [Related]
19. [Clinical aspects, diagnostic lung function and biochemical parameters in children with homozygous alpha 1-antitrypsin deficiency].
Heck B; Ebert W; Schulz V; Trefz G; Paul K
Pneumologie; 1990 Feb; 44 Suppl 1():418-9. PubMed ID: 2367424
[TBL] [Abstract][Full Text] [Related]
20. [Alpha 1-antitrypsin polymorphism].
Nowak S; Czech E; Cicha A
Postepy Hig Med Dosw; 1989; 43(2-4):213-35. PubMed ID: 2702353
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]