TY  - JOUR
AU  - Torres-Duran, Maria
AU  - Lopez-Campos, Jose Luis
AU  - Barrecheguren, Miriam
AU  - Miravitlles, Marc
AU  - Martinez-Delgado, Beatriz
AU  - Castillo, Silvia
AU  - Escribano, Amparo
AU  - Baloira, Adolfo
AU  - Navarro-Garcia, Maria Mercedes
AU  - Pellicer, Daniel
AU  - Bañuls, Lucia
AU  - Magallon, Maria
AU  - Casas, Francisco
AU  - Dasi, Francisco
PY  - 2018
DO  - 10.1186/s13023-018-0856-9
UR  - http://hdl.handle.net/10668/12702
T2  - Orphanet journal of rare diseases
AB  - Alpha-1 antitrypsin deficiency (AATD) is a rare hereditary condition that leads to decreased circulating alpha-1 antitrypsin (AAT) levels, significantly increasing the risk of serious lung and/or liver disease in children and adults, in which some...
LA  - en
PB  - BioMed Central Ltd.
KW  - Alpha-1 antitrypsin
KW  - Alpha-1 antitrypsin deficiency
KW  - Augmentation therapy
KW  - COPD
KW  - Cirrhosis
KW  - Panniculitis
KW  - Rare respiratory diseases
KW  - SERPINA1
KW  - Vasculitis
KW  - Animals
KW  - Fibrosis
KW  - Humans
KW  - Panniculitis
KW  - Pulmonary Disease, Chronic Obstructive
KW  - Vasculitis
KW  - alpha 1-Antitrypsin
KW  - alpha 1-Antitrypsin Deficiency
TI  - Alpha-1 antitrypsin deficiency: outstanding questions and future directions.
TY  - research article
VL  - 13
ER  -