International audienceThe French registry of patients with alpha-1 antitrypsin deficiency (AATD)-associated emphysema was launched in 2006. Here, we aimed to report on the baseline characteristics of these patients, their health-related quality of life (HRQoL) and factors associated with HRQoL. Another goal was to survey the practices of French physicians regarding augmentation therapy. We included 273 patients with AATD, emphysema, obstructive-pattern [forced expiratory volume in 1 sec/forced volume capacity (FEV1/FVC) < 0.7], FEV1 ≤ 80% predicted. Mean (SD) age was 51.8 (11.1) years, 240 (87.9%) of patients were smokers or ex-smokers, mean (SD) FEV1 was 40.5% (15.7) predicted. Mean (SD) SGRQ score was 49.0 (20.0) and was higher for female...
OBJECTIVE: To prepare new guidelines for the Canadian Thoracic Society (CTS) regarding severe alpha1...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decre...
Rationale: Alpha-1 antitrypsin deficiency (AATD) is characterized by decreased circulating levels or...
Financement : cette étude est financée par une subvention du laboratoire français du fractionnement ...
Background: Measures of health related quality of life (HRQoL) in patients with α1-antitrypsin defic...
Background: Alpha-1 antitrypsin deficiency (AATD) is a rare disease that is associated with an incre...
EARCO; Augmentation therapy; SurveyEARCO; Terapia de aumento; EncuestaEARCO; Teràpia d'augment; Enqu...
Background Augmentation therapy (AT) is the only specific treatment licensed for patients with al...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
Background: Alpha-1-antitrypsin (AT) deficiency is a hereditary disorder associated with pulmonary e...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
International audienceEndobronchial coil treatment (ECT) is a minimally invasive procedure developed...
International audienceRationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic co...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
OBJECTIVE: To prepare new guidelines for the Canadian Thoracic Society (CTS) regarding severe alpha1...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decre...
Rationale: Alpha-1 antitrypsin deficiency (AATD) is characterized by decreased circulating levels or...
Financement : cette étude est financée par une subvention du laboratoire français du fractionnement ...
Background: Measures of health related quality of life (HRQoL) in patients with α1-antitrypsin defic...
Background: Alpha-1 antitrypsin deficiency (AATD) is a rare disease that is associated with an incre...
EARCO; Augmentation therapy; SurveyEARCO; Terapia de aumento; EncuestaEARCO; Teràpia d'augment; Enqu...
Background Augmentation therapy (AT) is the only specific treatment licensed for patients with al...
Background: Severe hereditary alpha-1-antitrypsin deficiency (AATD) is a known risk factor for the e...
Background: Alpha-1-antitrypsin (AT) deficiency is a hereditary disorder associated with pulmonary e...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to...
International audienceEndobronchial coil treatment (ECT) is a minimally invasive procedure developed...
International audienceRationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic co...
Background and Objectives: Alpha 1-antitrypsin deficiency (AATD) is one of the genetic risk factors ...
OBJECTIVE: To prepare new guidelines for the Canadian Thoracic Society (CTS) regarding severe alpha1...
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decre...
Rationale: Alpha-1 antitrypsin deficiency (AATD) is characterized by decreased circulating levels or...