Nos tabagistas, os sintomas surgem ainda mais precocemente, cerca de 10 anos mais cedo. Estudos comparativos mostraram variados graus de pureza e de atividade in vitro. Novas perspectivas de tratamento. Registro internacional de AAT.

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Methods:: This was a cross-sectional study involving COPD patients 40 years of age or older, from five Brazilian states. In the sample as a whole, the overall prevalence of AATD was 2. Todos os pacientes foram submetidos a dosagem de AAT em amostras de sangue seco por meio de nefelometria. Figure 1. Flowchart of the patients included in the study and their distribution, by participating…. Figure 2. Flowchart of alpha 1-antitrypsin AAT deficiency screening and genotype distribution.

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Send even when there aren't any new results. Optional text in email:. Save Cancel. Create a file for external citation management software Create file Cancel. Full-text links Cite Favorites. Abstract in English , Portuguese. Figures Figure 1. Flowchart of the patients included…. Flowchart of alpha 1-antitrypsin AAT …. See this image and copyright information in PMC. Similar articles Sleep-disordered breathing in patients with COPD and mild hypoxemia: prevalence and predictive variables.

J Bras Pneumol. Caram LM, et al. Queiroz CF, et al. Alpha-1 Antitrypsin Deficiency. Stoller JK, et al. Long-term clinical outcomes following treatment with alpha 1-proteinase inhibitor for COPD associated with alpha-1 antitrypsin deficiency: a look at the evidence.

Rahaghi FF, Miravitlles M. Rahaghi FF, et al. Respir Res. Show more similar articles See all similar articles. Guerrina N, et al. Int J Mol Sci. The patient profile of individuals with Alpha-1 antitrypsine gene mutations at a referral center in Brazil. Felisbino MB, et al. Precision medicine in COPD: where are we and where do we need to go? Sidhaye VK, et al. Eur Respir Rev. Print Sep Diagnosing alpha-1 antitrypsin deficiency: does it prevent or improve the course of COPD?

Godoy I. No abstract available. The polymorphism of "prealbumins" and alphaantitrypsin in human sera. Clin Chim Acta. Assignment of the alpha 1-antitrypsin gene and a sequence-related gene to human chromosome 14 by molecular hybridization. Am J Hum Genet. Alpha1-antitrypsin deficiency. Worldwide racial and ethnic distribution of alpha1-antitrypsin deficiency summary of an analysis of published genetic epidemiologic surveys.

The pathogenesis of chronic obstructive lung diseases implications for therapy. Publication types Multicenter Study Actions. MeSH terms Aged Actions. Cross-Sectional Studies Actions.

Female Actions. Genotype Actions. Humans Actions. Male Actions. Middle Aged Actions. Prevalence Actions. Copy Download.


Deficiencia de alfa-1-antitripsina

Archivos de Bronconeumologia http: www. Other types of articles such as reviews, editorials, special articles, clinical reports, and letters to the Editor are also published in the Journal. It is a monthly Journal that publishes a total of 12 issues, which contain these types of articles to different extents. All manuscripts are sent to peer-review and handled by the Editor or an Associate Editor from the team. The Journal is published both in Spanish and English.


Prevalence of alpha-1 Antitrypsin Deficiency and Allele Frequency in Patients With COPD in Brazil


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