Introduction Alpha-1 antitrypsin deficiency (AATD), first described by Laurell and Eriksson in 1963 (1) , is an autosomal codominant hereditary disorder caused by a mutation in the SERPINA1 gene, which leads to dysregulation of neutrophil elastase…
Pulmonary3 He Magnetic Resonance Imaging Biomarkers of Regional Airspace Enlargement in Alpha-1 Antitrypsin Deficiency
This post is licensed under CC BY 4.0 by the author.
Recently Updated
- Neurometabolites Alteration in the Acute Phase of Mild Traumatic Brain Injury (mTBI)
- Reinforcing the Importance and Feasibility of Implementing a Low-dose Protocol for CT-guided Biopsies
- Rethinking the PGY-1 Basic Clinical Year
- Single Injection Dual-Phase Cone Beam CT (DP-CBCT) Vascular Anatomy Assessment and Occult Nodule Detection; Have We Reached the Focus?
- The Yellow Scale Is Superior to the Gray Scale for Detecting Acute Ischemic Stroke on a Monitor Display in Computed Tomography