Proposed Stages of Myocardial Phenotype Development in Fabry Disease.

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作者： Sabrina,Nordin ^[1] ; Rebecca,Kozor ^[2] ; Katia,Medina-Menacho ^[1] ; Amna,Abdel-Gadir ^[1] ; Shanat,Baig ^[3] ; Daniel M,Sado ^[4] ; Ilaria,Lobascio ^[5] ; Elaine,Murphy ^[6] ; Robin H,Lachmann ^[6] ; Atul,Mehta ^[7] ; Nicola C,Edwards ^[3] ; Uma,Ramaswami ^[7] ; Richard P,Steeds ^[3] ; Derralynn,Hughes ^[7] ; James C,Moon ^[8]

作者单位： Cardiology Department, Barts Heart Centre, London, United Kingdom; Institute of Cardiovascular Science, University College London, London, United Kingdom. ^[1] Sydney Medical School, University of Sydney, Sydney, Australia. ^[2] Cardiology Department, University Hospitals Birmingham, Birmingham, United Kingdom. ^[3] King's College London, London, United Kingdom. ^[4] Cardiology Department, Barts Heart Centre, London, United Kingdom. ^[5] Charles Dent Metabolic Unit, National Hospital for Neurology and Neurosurgery, London, United Kingdom. ^[6] Lysosomal Storage Disorder Unit, Royal Free Hospital, London, United Kingdom. ^[7] Cardiology Department, Barts Heart Centre, London, United Kingdom; Institute of Cardiovascular Science, University College London, London, United Kingdom. Electronic address: j.moon@ucl.ac.uk. ^[8]

关键词 Fabry disease gender native T1 phenotype