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  1. Urinary-derived extracellular vesicles reveal a distinct microRNA signature associated with the development and progression of Fabry nephropathy
  2. Renoprotective Effect of Agalsidase Alfa: A Long-Term Follow-Up of Patients with Fabry Disease
  3. Podocyturia in Fabry disease: a 10-year follow-up
  4. Urinary Extracellular Vesicles and Their miRNA Cargo in Patients with Fabry Nephropathy
  5. Characteristics of Vascular Phenotype in Fabry Patients
  6. Early indicators of disease progression in Fabry disease that may indicate the need for disease-specific treatment initiation: findings from the opinion-based PREDICT-FD modified Delphi consensus initiative
  7. Biomarkers of Fabry Nephropathy: Review and Future Perspective
  8. Cardiomyopathy and kidney function in agalsidase beta‐treated female Fabry patients: a pre‐treatment vs. post‐treatment analysis
  9. Switching from agalsidase alfa to pegunigalsidase alfa for treating Fabry disease: One year of treatment data from BRIDGE, a phase III open label study
  10. Aging in Fabry Disease: Role of Telomere Length, Telomerase Activity, and Kidney Disease
  11. Analysis of the baseline characteristics of Fabry disease patients screened for the pegunigalsidase alfa phase III BALANCE study
  12. Pegunigalsidase alfa for the treatment of Fabry disease: Preliminary results from a phase III open label, switch over study from agalsidase alfa
  13. Renal and cardiac outcomes in female patients with Fabry disease treated with agalsidase beta: A Fabry registry analysis of pre- versus post-treatment comparison
  14. Fabry disease: diagnostic methods in nephrology practice
  15. Paricalcitol as an Antiproteinuric Agent Can Result in the Deterioration of Renal and Heart Function in a Patient with Fabry Disease
  16. Renal Replacement Therapy in Slovenia: Excerpts From 2013 Data
  17. Anti-proteinuric therapy and Fabry nephropathy; factors associated with preserved kidney function during agalsidase-beta therapy
  18. Antiproteinuric therapy and Fabry nephropathy: factors associated with preserved kidney function during agalsidase-beta therapy
  19. Recommendation for initiation and cessation of enzyme replacement therapy
  20. Exocrine pancreatic insufficiency is not a cause of abdominal complaints in patients with Fabry disease
  21. Recommendations for initiation and cessation of enzyme replacement therapy in patients with Fabry disease: the European Fabry Working Group consensus document
  22. Exocrine pancreatic insufficiency is not a cause of abdominal complaints in patients with fabry disease
  23. Renal Replacement Therapy in Slovenia: Excerpts From 2011 Data
  24. Recommendations on Reintroduction of Agalsidase Beta for Patients with Fabry Disease in Europe, Following a Period of Shortage
  25. Could Iron Deficiency Also Affect Platelet-Related Hemostasis Impairment in Hemodialysis Patients?: Reply
  26. Renal outcomes of agalsidase beta treatment for Fabry disease: role of proteinuria and timing of treatment initiation
  27. Urinary Total Globotriaosylceramide and Isoforms to Identify Women With Fabry Disease: A Diagnostic Test Study
  28. Prognostic Indicators of Renal Disease Progression in Adults with Fabry Disease: Natural History Data from the Fabry Registry
  29. Association Between Platelet-Related Hemostasis Impairment and Functional Iron Deficiency in Hemodialysis Patients
  30. 143. End stage renal disease in patients with Fabry disease: Natural history data from the Fabry registry
  31. End-stage renal disease in patients with Fabry disease: natural history data from the Fabry Registry
  32. Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN)
  33. A successful treatment of life-threatening bleeding from polycystic kidneys with antifibrinolytic agent tranexamic acid
  34. Epoetin Responsiveness in Peritoneal Dialysis Patients: A Multi-center Slovenian Study
  35. The effect of long term, low-dose tranexamic acid treatment on platelet dysfunction and haemoglobin levels in haemodialysis patients
  36. The study of anaemia-related haemostasis impairment in haemodialysis patients by in vitro closure time test
  37. Remarkable variability in renal disease in a large Slovenian family with Fabry disease
  38. Severe Diabetic Ketoacidosis Associated With Acute Myocardial Necrosis
  39. Tranexamic acid is beneficial as adjunctive therapy in treating major upper gastrointestinal bleeding in dialysis patients
  40. Treatment of subdural and intracerebral haematomas in a haemodialysis patient with tranexamic acid
  41. Successful treatment of bleeding from colonic angiodysplasias with tranexamic acid in a hemodialysis patient