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.
44. Sex-specific differences in emphysema using a murine antisense oligonucleotide model of α-1 antitrypsin deficiency. Joshi R; Ojha M; Lewis J; Fan Q; Monia B; Guo S; Varisco BM Am J Physiol Lung Cell Mol Physiol; 2019 Jun; 316(6):L1165-L1173. PubMed ID: 31017014 [TBL] [Abstract][Full Text] [Related]
45. Alpha one antitrypsin deficiency: from gene to treatment. Wood AM; Stockley RA Respiration; 2007; 74(5):481-92. PubMed ID: 17671403 [TBL] [Abstract][Full Text] [Related]
46. [A case from general practice (57). Lung emphysema in alpha 1-antitrypsin deficiency]. Kamber V Schweiz Rundsch Med Prax; 1986 Jun; 75(26):804-5. PubMed ID: 3489266 [No Abstract] [Full Text] [Related]
47. [Often overlooked alpha 1-antitrypsin deficiency emphysema. Early diagnosis could improve the prognosis]. MMW Fortschr Med; 2005 May; 147(18):50-1. PubMed ID: 15934592 [No Abstract] [Full Text] [Related]
52. Laboratory testing of individuals with severe alpha1-antitrypsin deficiency in three European centres. Miravitlles M; Herr C; Ferrarotti I; Jardi R; Rodriguez-Frias F; Luisetti M; Bals R Eur Respir J; 2010 May; 35(5):960-8. PubMed ID: 20436173 [TBL] [Abstract][Full Text] [Related]
53. Alpha-1 antitrypsin deficiency: pathogenesis, clinical presentation, diagnosis, and treatment. Köhnlein T; Welte T Am J Med; 2008 Jan; 121(1):3-9. PubMed ID: 18187064 [TBL] [Abstract][Full Text] [Related]
54. [Congenital alpha 1-antitrypsin deficiency as an aggravating factor in alveolar injury from cigarette smoke]. Massi G; Cotumaccio R; Auconi P Minerva Med; 1982 Sep; 73(36):2383-5. PubMed ID: 6981079 [No Abstract] [Full Text] [Related]
55. Compound heterozygosity for alpha-1-antitrypsin (S(iiyama) and QO(clayton)) in an Oriental patient. Miyahara N; Seyama K; Sato T; Fukuchi Y; Eda R; Takeyama H; Harada M Intern Med; 2001 Apr; 40(4):336-40. PubMed ID: 11334395 [TBL] [Abstract][Full Text] [Related]
56. Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis. Lodewyckx L; Vandevyver C; Vandervorst C; Van Steenbergen W; Raus J; Michiels L Hum Mutat; 2001 Sep; 18(3):243-50. PubMed ID: 11524735 [TBL] [Abstract][Full Text] [Related]
57. Alpha-1 Antitrypsin Deficiency Associated with the PI*Q0 Tubío-Pérez RA; Blanco-Pérez M; Ramos-Hernández C; Torres-Durán M Arch Bronconeumol (Engl Ed); 2018 Apr; 54(4):228-230. PubMed ID: 29122334 [No Abstract] [Full Text] [Related]
58. Emphysema associated with complete absence of alpha 1- antitrypsin in serum and the homozygous inheritance [corrected] of a stop codon in an alpha 1-antitrypsin-coding exon. Satoh K; Nukiwa T; Brantly M; Garver RI; Hofker M; Courtney M; Crystal RG Am J Hum Genet; 1988 Jan; 42(1):77-83. PubMed ID: 3257351 [TBL] [Abstract][Full Text] [Related]
59. A new variant of alpha-1-antitrypsin deficiency (Siiyama) associated with pulmonary emphysema. Takabe K; Seyama K; Shinada H; Nouchi T; Miyahara Y; Nukiwa T; Miyake K; Tsukimoto K; Ichioka M; Marumo F Intern Med; 1992 May; 31(5):702-7. PubMed ID: 1504439 [TBL] [Abstract][Full Text] [Related]
60. Homozygous and heterozygous alpha-1-antitrypsin deficiency: prevalence in pulmonary emphysema. Hutchison DC Proc R Soc Med; 1976 Feb; 69(2):130-1. PubMed ID: 1083529 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]