Päivi Pietilä-Effati
Publications
- Genetics, cardiac phenotype and cardiovascular outcomes in Fabry disease patients in Finland (2025)
- ESC Heart Failure
(A1 Refereed original research article in a scientific journal) - Magnetic Resonance Imaging in the Assessment of the Risk of Sudden Death in Cardiac Sarcoidosis: What Is Extensive or Significant Late Gadolinium Enhancement? (2025)
- Circulation: Arrhythmia and Electrophysiology
(A1 Refereed original research article in a scientific journal) - End-Stage Heart Failure in Cardiac Sarcoidosis (2024)
- Circulation
(A1 Refereed original research article in a scientific journal) - Long-term effectiveness of enzyme replacement therapy in Fabry disease with the p.Arg227Ter variant: Fabry disease in Ostrobothnia (FAST) study (2023)
- American Journal of Medical Genetics Part A
(A1 Refereed original research article in a scientific journal) - Incidence of Sudden Cardiac Death and Life-Threatening Arrhythmias in Clinically Manifest Cardiac Sarcoidosis With and Without Current Indications for an Implantable Cardioverter Defibrillator (2022)
- Circulation
(A1 Refereed original research article in a scientific journal) - Pulmonary manifestations and the effectiveness of enzyme replacement therapy in Fabry Disease with the p. Arg227Ter (p.R227*) mutation (2022)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal) - Renal denervation in patients who do not respond to cardiac resynchronization therapy (2022)
- Scandinavian Cardiovascular Journal
(A1 Refereed original research article in a scientific journal) - Cardiac Involvement in Fabry Disease: JACC Review Topic of the Week (2021)
- Journal of the American College of Cardiology
(A2 Refereed review article in a scientific journal ) - Manifestations and Outcome of Cardiac Sarcoidosis and Idiopathic Giant Cell Myocarditis by 25-Year Nationwide Cohorts (2021)
- Journal of the American Heart Association
(A1 Refereed original research article in a scientific journal) - Natural course of Fabry disease with the p Arg227Ter (pR227*) mutation in Finland: Fast study (2019)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal)



