Peter J. Schwartz
0000-0003-0367-1048
University of Milan
450 papers found
Refreshing results…
A statement of intent on the formation of the NCRP on Cardiovascular and Metabolic Disease: A new initiative to fight heart disease, stroke, diabetes and obesity in South Africa
Gene symbol: KCNH2.
Overlap between LQT3 and Brugada syndrome: Clinical features in a common mutation and underlying biophysical mechanisms
Gene symbol: SCN5A.
Highly malignant perinatal variant of long-QT syndrome caused by a profoundly dysfunctional SCN5A mutation successfully treated with mexiletine and propranolol
Long QT syndrome as a cause of stillbirths
Efficacy and safety of vernakalant hydrochloride injection for the treatment of atrial fibrillation after valvular or coronary artery bypass surgery
Electrocardiographic and genetic screening for long QT syndrome: Results from a prospective study on 44,596 neonates
Intronic branch point mutations, affecting splicing, can cause the Long QT Syndrome
The common LQT1 mutation KCNQ1/A341V predicts high risk of cardiac events in different ethnic backgrounds
Heart rate turbulence onset after atrial premature complexes does not reflect cardiac autonomic regulations in postinfarction patients
KCNJ2-Specific ECG abnormalities in type 1 Andersen-Tawil syndrome: The enlarged U wave, prolonged QU interval and left ventricular arrhythmias
Chronic vagal stimulation in patients with heart failure is feasible, safe and appears beneficial
Heart-Rate Profile During Exercise as a Predictor of Sudden Death
Discussion
The long QT syndrome: A clinical counterpart of hERG mutations
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