Results 161 to 170 of about 124,197,172 (205)

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 and Bronchial Asthma: Current Challenges. [PDF]

Biomolecules
Lopez-Campos JL, Muñoz-Sánchez B, Ferrer-Galván M, Quintana-Gallego E.   +3 more
europepmc   +1 more source

Alpha-1-antitrypsin deficiency

, 2018
openaire   +1 more source

Resolution of the circulating pathogenic phenotype of alpha-1 antitrypsin deficiency following liver transplantation

Heyer-Chauhan N, Ronzoni R, Aldobiyan I, Miranda E, Marshall A, Hurst JR, Irving JA, Lomas DA.   +7 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
openaire   +3 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.
James Ralph, Tomás P. Carroll, Alex Franciosi   +2 more
exaly   +3 more sources

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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.
SK Kabra, Rakesh Lodha, Kana Jat
  +5 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 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 in childhood

Current Problems in Pediatrics, 1980
alpha 1AT deficiency predisposes children to liver injury and adults to emphysema. Pi typing has clarified that the inherited deficiency is codominant. Amniocentesis is unproved as a reliable technique in detecting the homozygous deficient patient (another controversial issue).
J S, Latimer, H L, Sharp
openaire   +2 more sources