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.
214 related articles for article (PubMed ID: 35327571)
21. 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 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. Three new alpha1-antitrypsin deficiency variants help to define a C-terminal region regulating conformational change and polymerization. Fra AM; Gooptu B; Ferrarotti I; Miranda E; Scabini R; Ronzoni R; Benini F; Corda L; Medicina D; Luisetti M; Schiaffonati L PLoS One; 2012; 7(6):e38405. PubMed ID: 22723858 [TBL] [Abstract][Full Text] [Related]
24. The Importance of N186 in the Alpha-1-Antitrypsin Shutter Region Is Revealed by the Novel Bologna Deficiency Variant. Ronzoni R; Ferrarotti I; D'Acunto E; Balderacchi AM; Ottaviani S; Lomas DA; Irving JA; Miranda E; Fra A Int J Mol Sci; 2021 May; 22(11):. PubMed ID: 34073489 [TBL] [Abstract][Full Text] [Related]
25. The effects of weekly augmentation therapy in patients with PiZZ α1-antitrypsin deficiency. Schmid ST; Koepke J; Dresel M; Hattesohl A; Frenzel E; Perez J; Lomas DA; Miranda E; Greulich T; Noeske S; Wencker M; Teschler H; Vogelmeier C; Janciauskiene S; Koczulla AR Int J Chron Obstruct Pulmon Dis; 2012; 7():687-96. PubMed ID: 23055718 [TBL] [Abstract][Full Text] [Related]
34. New Findings in PiZZ alpha1-antitrypsin deficiency-related panniculitis. Demonstration of skin polymers and high dosing requirements of intravenous augmentation therapy. Gross B; Grebe M; Wencker M; Stoller JK; Bjursten LM; Janciauskiene S Dermatology; 2009; 218(4):370-5. PubMed ID: 19218787 [TBL] [Abstract][Full Text] [Related]
35. Serum Levels of Glutamate-Pyruvate Transaminase, Glutamate-Oxaloacetate Transaminase and Gamma-Glutamyl Transferase in 1494 Patients with Various Genotypes for the Alpha-1 Antitrypsin Gene. Hernández Pérez JM; Blanco I; Jesús Sánchez Medina A; Díaz Hernández L; Antonio Pérez Pérez J J Clin Med; 2020 Dec; 9(12):. PubMed ID: 33287251 [TBL] [Abstract][Full Text] [Related]
36. The discovery of α1-antitrypsin and its role in health and disease. Janciauskiene SM; Bals R; Koczulla R; Vogelmeier C; Köhnlein T; Welte T Respir Med; 2011 Aug; 105(8):1129-39. PubMed ID: 21367592 [TBL] [Abstract][Full Text] [Related]
37. Prevalence of alpha-1 antitrypsin deficiency and allele frequency in patients with COPD in Brazil. Russo R; Zillmer LR; Nascimento OA; Manzano B; Ivanaga IT; Fritscher L; Lundgren F; Miravitlles M; Gondim HD; Santos G; Alves MA; Oliveira MV; Souza AA; Sales MP; Jardim JR J Bras Pneumol; 2016; 42(5):311-316. PubMed ID: 27812629 [TBL] [Abstract][Full Text] [Related]
38. Alpha-1-antitrypsin deficiency: Genetic variations, clinical manifestations and therapeutic interventions. Hazari YM; Bashir A; Habib M; Bashir S; Habib H; Qasim MA; Shah NN; Haq E; Teckman J; Fazili KM Mutat Res Rev Mutat Res; 2017 Jul; 773():14-25. PubMed ID: 28927525 [TBL] [Abstract][Full Text] [Related]
39. Alpha-1-antitrypsin deficiency. Bals R Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):629-33. PubMed ID: 20955965 [TBL] [Abstract][Full Text] [Related]
40. Activation of complement component 3 is associated with airways disease and pulmonary emphysema in alpha-1 antitrypsin deficiency. O'Brien ME; Fee L; Browne N; Carroll TP; Meleady P; Henry M; McQuillan K; Murphy MP; Logan M; McCarthy C; McElvaney OJ; Reeves EP; McElvaney NG Thorax; 2020 Apr; 75(4):321-330. PubMed ID: 31959730 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]