Results 181 to 190 of about 26,458 (238)

Protein Aggregates in Heterozygous Alpha-1 Antitrypsin Phenotype Is a Marker for Progressive Disease. [PDF]

Gastro Hep Adv
Marek GW, Malhi H.
europepmc   +1 more source

Alpha 1 Antitrypsin Suppresses Autoantibody Production and Cellular Autoimmunity in Chronic Graft-Versus-Host Disease (cGVHD) in a Lupus Mouse Model. [PDF]

Biomolecules
Elshikha AS, Abboud G, Stokes J, Arnold C, Kanda N, Morel L, Song S.   +6 more
europepmc   +1 more source

A Case of Acetaminophen Toxicity in a Patient With an Unusual Alpha-1 Antitrypsin Phenotype. [PDF]

Cureus
Agrawal A, Chowdhury M, Winkie C, Vijay C.   +3 more
europepmc   +1 more source

Quantitative CT of emphysema, wall thickness and mucus plugs in alpha-1-antitrypsin deficiency: relationship to clinical outcomes. [PDF]

Eur Radiol
Dournes G, Hadj Bouzid AI, Doucet K, Benlala I, Maurac A, Blanchard E, Dupin I, Berger P, Henrot P, Zysman M.   +9 more
europepmc   +1 more source

Strawberry Gingivitis as the Initial Manifestation of Granulomatosis with Polyangiitis in A Patient with Alpha-1 Antitrypsin Deficiency. [PDF]

Eur J Case Rep Intern Med
Haque A, Naveed HK, Padrangi G, Gulzar L, Patel H, Motiani V, Solanki S.   +6 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 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