Synopsis of recent research by authors named "Annie Haillot"
- Annie Haillot's research primarily focuses on alpha-1 antitrypsin deficiency (AATD), exploring genetic variants and serum level variability, to enhance understanding and diagnostic approaches for this condition.
- In the article "The Null Q0 Variant within a Copy-Neutral Loss-of-Heterozygosity Event Causing Alpha-1 Antitrypsin Deficiency," she examines specific genetic mutations contributing to AATD, which may have implications for treatment and patient management.
- Her study titled "IntraIndividual Variability in Serum Alpha-1 Antitrypsin Levels" evaluates the reliability of AAT serum level measurements and how variations correlate with inflammation, providing valuable insights for clinicians in assessing AATD.