@article{johansson2015adult,
  title = {Adult Fabry patients in Sweden - Baseline data and Outcome of Four-Year Enzyme Replacement Treatment in a Male Cohort without Proteinuria},
  author = {Jan-Ove Johansson and Jarl Ahlmén and Anita Persson and Kenneth Caidahl and Jan-Eric Månsson},
  year = 2015,
  url = {https://ibimapublishing.com/articles/JMED/2015/373829/},
  journal = {JMED Research},
  volume = 2015 (2015),
  pages = 15,
  doi = 10.5171/2015.373829,
  abstract = {Background: Fabry disease is a rare X-linked lysosomal storage disease caused by defective activity of the lysosomal enzyme α-galactosidase A. The objective was to study the baseline characteristics of Fabry patients in Sweden, Furthermore, to study the effect of 4 years of ERT (enzyme replacement therapy) in an open study of a subcohort of Fabry men with no or mild proteinuria (},
  keywords = {Fabry disease, lysosomal storage disease, enzyme replacement therapy (ERT).},
  note = Article ID: 373829
}