La sindrome del QT lungo (LQTS) è una malattia genetica non frequente (riguarda un neonato ogni 2.000)[1]Schwartz PJ, Malliani A. Electrical alternation

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Divet P, Maury P, Beneyto M. Department of Cardiology, Toulouse University Hospital, Toulouse, France. Un’infermiera di 25 anni riferiva cardiopalmo fastidioso. Non

Xiao YY, Tang MX, Tang Y. Department of Cardiology, Hunan Provincial Peoplès Hospital, The First Affiliated Hospital of Hunan Normal University, Clinical

Gabarin M, Divakara Menon S. Cardiology Division, Hamilton Health Sciences, Arrhythmia Service Unit, Mc-Master University, Hamilton, Canada and Cardiology Department, Meir Medical

Ramakumar V, Gupta A, Jain A. Department of Cardiology, Dr Rela Institute & Medical Center, Chennai, India, and Department of Cardiology, Vardhman

Trongtorsak A, Ellenbogen K, Pillai A. Divisions of Cardiology and Cardiac Electrophysiology Pauley Heart Center, Virginia Commonwealth University, Richmond (USA) Un uomo

Roig A, de Andrade AT. EKGDX, Miami e Hospital do Coração de Messejana, Fortaleza, Brazil. Una signora di 74 anni, ipertesa, viene

Luckmann J, Win S, Ajagbe T, Samarawickrama T Cardiology, University of Exeter Medical School, Truro, GBR, Cardiology, Royal Cornwall Hospital, Truro, GBR

Liu Y-S, ChinWei Tan S, Zhao Y-T – Department of Cardiology, Peking University Aerospace School of Clinical Medicine (Aerospace Center Hospital) and