Centro Alfa-1 Granada

Are there differences between the available treatments for pulmonary emphysema due to Alpha-1 antitrypsin deficiency?

An editorial has recently been published in the Archives of Bronchopneumology that analyzes the differences between the approved treatments for the treatment of pulmonary emphysema due to Alpha-1 deficiency. Esquinas C, Miravitlles M. Arch Bronconeumol. 2018;54:451-452. This publication reflects the differences between the approved treatments for pulmonary emphysema due to Alpha-1 atitrypsin deficiency in Spain,

Are there differences between the available treatments for pulmonary emphysema due to Alpha-1 antitrypsin deficiency? Read More »

The Alfa-1 association in Spain continues with its magnificent work of spreading the Alpha-1 antitrypsin deficit among patients, relatives and health professionals interested

On this occasion, two meetings will be held in Andalusia to update knowledge about the Alpha-1 Antitrypsin Deficit next May. It has the collaboration of the Alfa-1 Center of Andalusia in Granada and Seville, as well as REDAAT. You can find more information on the following button: Read more

The Alfa-1 association in Spain continues with its magnificent work of spreading the Alpha-1 antitrypsin deficit among patients, relatives and health professionals interested Read More »

Alpha-1 antitrypsin Pi*SZ genotype: estimated prevalence and number of SZ subjects worldwide. Ignacio Blanco et al. International Journal of COPD. 2017;12:1683-1694.

In this study the prevalence of the Pi * SZ genotype is estimated worldwide, statistics in studies of previous populations. 262 cohorts from 71 countries are included for analysis. The allowed data from these cohorts allow estimating the existence of almost 1,500,000 Pi * SZ individuals worldwide, the majority (48%) in Europe, 39% in America

Alpha-1 antitrypsin Pi*SZ genotype: estimated prevalence and number of SZ subjects worldwide. Ignacio Blanco et al. International Journal of COPD. 2017;12:1683-1694. Read More »

Recommendations for the search for solutions in the field of Rare Diseases

Download document In January 2017, more than 30 organizations presented this document of proposals with the aim of establishing active and permanent platforms that jointly enable effective solutions to be found between the competent public authorities, political representatives and all the groups belonging to the field. of rare, minority or infrequent diseases and, thus, be

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