Results 141 to 150 of about 26,843 (195)

Co-occurrence of Alpha-1 Antitrypsin Deficiency (AATD) and Common Variable Immunodeficiency (CVID): A Case Report. [PDF]

Cureus
Aynaci A, Tepetam FM, Cetinkaya E, Yildirim N, Özden Ş.   +4 more
europepmc   +1 more source

Alpha‐1‐Antitrypsin Deficiency [PDF]

Clinical Liver Disease, 2022
Content available: Author Audio Recording.
Anandini Suri, Dhiren Patel, Jeffery Teckman   +2 more
core   +5 more sources

Alpha 1 antitrypsin to treat lung disease in alpha 1 antitrypsin deficiency: recent developments and clinical implications

International Journal of COPD, 2018
Kenneth R Chapman,1 Joanna Chorostowska-Wynimko,2 A Rembert Koczulla,3 Ilaria Ferrarotti,4 Noel G McElvaney5 1Department of Medicine, University of Toronto, Toronto, ON, Canada; 2Department of Genetics and Clinical Immunology, National Institute of ...
, Joanna Chorostowska-Wynimko, Andreas Rembert Koczulla   +2 more
exaly   +2 more sources

Alpha-1 antitrypsin deficiency–associated panniculitis

Journal of the American Academy of Dermatology, 2022
Background: Panniculitis represents a rare and potentially lethal manifestation of alpha-1 antitrypsin deficiency (AATD). Evidence regarding management is limited to case reports and small case series.
Alessandro N Franciosi, James Ralph, Christian Gulmann   +2 more
exaly   +2 more sources

Alpha-1 antitrypsin deficiency [PDF]

The Nurse Practitioner, 2014
Chair of Pneumology and Allergology, Department of Internal Medicine, State University of Medicine and Pharmacy "NicolaeTestemitanu", Chisinau, Republic of MoldovaIntroduction: Alpha-1-antitrypsin deficiency (A1AD) is a hereditary disorder, caused by ...
Cathy R, Kessenich, Kathryn, Bacher
openaire   +3 more sources

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Alpha-1-antitrypsin augmentation therapy for alpha-1-antitrypsin deficiency

The American Journal of Medicine, 1988
Alpha-1-antitrypsin (A1AT) deficiency is a genetic disorder characterized by low serum levels of A1AT and a high risk for the development of emphysema. A1AT is the principal inhibitor of neutrophil elastase, such that a deficiency of A1AT results in insufficient anti-elastase protection in the lower respiratory tract, thus allowing neutrophil elastase ...
R C, Hubbard, R G, Crystal
openaire   +2 more sources

Alpha-1 Antitrypsin Deficiency

2023
Alpha-1 antitrypsin (AAT) deficiency is a common monogenic disorder in which there is a strong founder effect of a single missense mutation in SERPINA1, the gene encoding this major circulating serum anti-protease that is normally expressed primarily in hepatocytes.
Alisha M, Gruntman, Wen, Xue, Terence R, Flotte   +2 more
openaire   +2 more sources

Alpha-1-antitrypsin in malakoplakia

Virchows Archiv A Pathological Anatomy and Histology, 1982
Macrophages in malakoplakia contain large amounts of immunoreactive alpha-1-antitrypsin (AAT). The amount of AAT remains unchanged during the morphogenetic stages of the pathological process (early, granulomatous, fibrosing phases), and does not correlate with the number or the presence of Michaelis-Gutmann (M.G.) bodies.
F, Callea, B, Van Damme, V J, Desmet
openaire   +2 more sources

Alpha-1 Antitrypsin Deficiency

Journal of Insurance Medicine, 2015
Alpha-1 antitrypsin deficiency is an inherited disorder that may cause severe lung and liver disease.
openaire   +2 more sources