147 related articles for article (PubMed ID: 2036855)
1. Intermediate alpha 1-antitrypsin deficiency with apical lung bullae and spontaneous pneumothorax. Presence of a Z variant in an American black.
Mostafavi S; Lieberman J
Chest; 1991 Jun; 99(6):1545-6. PubMed ID: 2036855
[TBL] [Abstract][Full Text] [Related]
2. Spontaneous pneumothorax in flight as first manifestation of alpha-1 antitrypsin deficiency.
Lin YC; Chiu WK; Chang H; Cheng YL; Chen JC
Aviat Space Environ Med; 2008 Jul; 79(7):704-6. PubMed ID: 18619132
[TBL] [Abstract][Full Text] [Related]
3. Surgical pathology of bullae with and without pneumothorax.
Keszler P
Eur J Cardiothorac Surg; 1988; 2(6):416-24. PubMed ID: 3272248
[TBL] [Abstract][Full Text] [Related]
4. Alpha-1 antitrypsin deficiency and spontaneous pneumothorax: possible causal relationship.
Serapinas D; Obrikyte V; Vaicius D; Balciuviene R; Valavicius A; Sakalauskas R
Pneumologia; 2014; 63(1):32-5. PubMed ID: 24800593
[TBL] [Abstract][Full Text] [Related]
5. Null allele alpha-1 antitrypsin deficiency: case report of the total pleural covering technique for disease-associated pneumothorax.
Kusu T; Nakagiri T; Minami M; Shintani Y; Kadota Y; Inoue M; Sawabata N; Okumura M
Gen Thorac Cardiovasc Surg; 2012 Jul; 60(7):452-5. PubMed ID: 22544422
[TBL] [Abstract][Full Text] [Related]
6. Alpha 1-antitrypsin Pi-types in 965 COPD patients.
Lieberman J; Winter B; Sastre A
Chest; 1986 Mar; 89(3):370-3. PubMed ID: 3485034
[TBL] [Abstract][Full Text] [Related]
7. Alpha1-antitrypsin deficiency. 2: genetic aspects of alpha(1)-antitrypsin deficiency: phenotypes and genetic modifiers of emphysema risk.
DeMeo DL; Silverman EK
Thorax; 2004 Mar; 59(3):259-64. PubMed ID: 14985567
[TBL] [Abstract][Full Text] [Related]
8. Liver Phenotypes of European Adults Heterozygous or Homozygous for Pi∗Z Variant of AAT (Pi∗MZ vs Pi∗ZZ genotype) and Noncarriers.
Schneider CV; Hamesch K; Gross A; Mandorfer M; Moeller LS; Pereira V; Pons M; Kuca P; Reichert MC; Benini F; Burbaum B; Voss J; Gutberlet M; Woditsch V; Lindhauer C; Fromme M; Kümpers J; Bewersdorf L; Schaefer B; Eslam M; Bals R; Janciauskiene S; Carvão J; Neureiter D; Zhou B; Wöran K; Bantel H; Geier A; Dirrichs T; Stickel F; Teumer A; Verbeek J; Nevens F; Govaere O; Krawczyk M; Roskams T; Haybaeck J; Lurje G; Chorostowska-Wynimko J; Genesca J; Reiberger T; Lammert F; Krag A; George J; Anstee QM; Trauner M; Datz C; Gaisa NT; Denk H; Trautwein C; Aigner E; Strnad P;
Gastroenterology; 2020 Aug; 159(2):534-548.e11. PubMed ID: 32376409
[TBL] [Abstract][Full Text] [Related]
9. Heteropolymerization of α-1-antitrypsin mutants in cell models mimicking heterozygosity.
Laffranchi M; Berardelli R; Ronzoni R; Lomas DA; Fra A
Hum Mol Genet; 2018 May; 27(10):1785-1793. PubMed ID: 29538751
[TBL] [Abstract][Full Text] [Related]
10. [A Rare Cause of a Spontaneous Pneumothorax].
Lepiorz M; Großer C; Hofmann HS; Pfeifer M
Pneumologie; 2017 Sep; 71(9):590-593. PubMed ID: 28753703
[TBL] [Abstract][Full Text] [Related]
11. Recurrent spontaneous pneumothorax in pulmonary histiocytosis X.
Minghini A; Trogdon SD
Am Surg; 1998 Nov; 64(11):1040-2. PubMed ID: 9798765
[TBL] [Abstract][Full Text] [Related]
12. [The histopathology of apical bullae, sources of spontaneous pneumothorax].
Keszler P; Appel J
Bronches; 1974; 24(3):151-8. PubMed ID: 4411162
[No Abstract] [Full Text] [Related]
13. Alpha 1-antitrypsin deficiency: the radiological features of pulmonary emphysema in subjects of Pi type Z and Pi type SZ: a survey by the British Thoracic Association.
Gishen P; Saunders AJ; Tobin MJ; Hutchison DC
Clin Radiol; 1982 Jul; 33(4):371-7. PubMed ID: 6979454
[TBL] [Abstract][Full Text] [Related]
14. The role of proteases, endoplasmic reticulum stress and SERPINA1 heterozygosity in lung disease and α-1 anti-trypsin deficiency.
Greene CM; Hassan T; Molloy K; McElvaney NG
Expert Rev Respir Med; 2011 Jun; 5(3):395-411. PubMed ID: 21702661
[TBL] [Abstract][Full Text] [Related]
15. [Usefulness of computed tomography in determining risk of recurrence after a first episode of primary spontaneous pneumothorax: therapeutic implications].
Martínez-Ramos D; Angel-Yepes V; Escrig-Sos J; Miralles-Tena JM; Salvador-Sanchís JL
Arch Bronconeumol; 2007 Jun; 43(6):304-8. PubMed ID: 17583639
[TBL] [Abstract][Full Text] [Related]
16. α-1 Antitrypsin Genotype-Phenotype Discrepancy in a 42-Year-Old Man Who Carries the Null-Allele.
Pavičić T; Ćelap I; Njegovan M; Tešija Kuna A; Štefanović M
Lab Med; 2020 May; 51(3):301-305. PubMed ID: 31583408
[TBL] [Abstract][Full Text] [Related]
17. [Alpha-1 antitrypsin deficiency and spontaneous pneumothorax. Just a coincidence?].
Menga G; Girbal MS; Montoto Piazza L; Fernández ME
Medicina (B Aires); 2020; 80(5):473-478. PubMed ID: 33048791
[TBL] [Abstract][Full Text] [Related]
18. Placental transmogrification of the lung presenting as giant bullae with soft-fatty components.
Santana AN; Canzian M; Stelmach R; Jatene FB
Eur J Cardiothorac Surg; 2008 Jan; 33(1):124-6. PubMed ID: 17983762
[TBL] [Abstract][Full Text] [Related]
19. alpha 1-antitrypsin deficiency and idiopathic pulmonary fibrosis in a family.
Kim H; Lepler L; Daniels A; Phillips Y
South Med J; 1996 Oct; 89(10):1008-10. PubMed ID: 8865799
[TBL] [Abstract][Full Text] [Related]
20. α1-antitrypsin deficiency in fraternal twins born with familial spontaneous pneumothorax.
Greene DN; Procter M; Krautscheid P; Mao R; Lyon E; Grenache DG
Chest; 2012 Jan; 141(1):239-241. PubMed ID: 22215832
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
