Case Report: α1-antitrypsin deficiency causing persistent pleural effusion and multilobar alveolar emphysema in a young dog. [PDF]
Doulidis PG +8 more
europepmc +1 more source
Plasma proteome correlations with liver stiffness in pediatric cholestasis implicate epithelial to mesenchymal transition. [PDF]
Shneider BL +22 more
europepmc +1 more source
Rare but relevant: Genetic liver disease in the general medical setting. [PDF]
Allouni S, Ala A.
europepmc +1 more source
Alpha-1 antitrypsin in COVID-19 patients: a dual-center screening study in Malaysia. [PDF]
Musa N +9 more
europepmc +1 more source
Stereo-random oligonucleotides enable efficient recruitment of ADAR in vitro and in vivo. [PDF]
Pfeiffer LS +17 more
europepmc +1 more source
Alpha1-Antitrypsin in Lung Diseases: A Cross-Sectional Observational Study. [PDF]
Páska C +8 more
europepmc +1 more source
Alpha-1 antitrypsin deficiency with the rare IZ phenotype presenting as cystic lung disease. [PDF]
Reed TJ, Shisler R, Collins J.
europepmc +1 more source
Partially Replacing Dietary Carbohydrate With Unsaturated Fat or Protein Shifts Protein-Based HDL Subspecies Toward Lower Coronary Heart Disease Risk. [PDF]
Zhang B +9 more
europepmc +1 more source
The article presents a clinical lecture on alpha-1-antitrypsin (A1AT) deficiency, a genetically determined disease caused by A1AT deficiency in blood serum and manifested in the form of chronic obstructive pulmonary disease, emphysema, liver and vascular
Надежда Григорьевна Ганюкова +5 more
doaj
Next-Generation Regenerative Therapies for Alpha-1 Antitrypsin Deficiency: Molecular Pathogenesis to Clinical Translation. [PDF]
Yang SR, Kim HR.
europepmc +1 more source

