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Chiara Ferrandi

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Disorders

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Peter J Schwartz; Emilio Vanoli; Lia Crotti; Carla Spazzolini; Chiara Ferrandi; Althea Goosen; Paula Hedley; Marshall Heradien; Sara Bacchini; A Turco; Maria Teresa La Rovere; Antonella Bartoli; Alfred L George; Paul A Brink
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome.
Troy E Rhodes; Robert L Abraham; Richard C Welch; Carlos G Vanoye; Lia Crotti; Marianne Arnestad; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Ashild Vege; Torleiv O Rognum; Dan Mark Roden; Peter J Schwartz; Alfred L George
Cardiac potassium channel dysfunction in sudden infant death syndrome.
Lia Crotti; Chiara Ferrandi; Roberto Insolia; Matteo Pedrazzini; E Andreoli; Alessia Veia; Gabriele Crimi; A Agnetti; Gaetano M De Ferrari; Peter J Schwartz
Gene symbol: SCN5A.

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All Publications

2008: Peter J Schwartz; Emilio Vanoli; Lia Crotti; Carla Spazzolini; Chiara Ferrandi; Althea Goosen; Paula Hedley; Marshall Heradien; Sara Bacchini; A Turco; Maria Teresa La Rovere; Antonella Bartoli; Alfred L George; Paul A Brink
Neural control of heart rate is an arrhythmia risk modifier in long QT syndrome.
Journal of the American College of Cardiology 2008;51(9):920-9.
2008: Troy E Rhodes; Robert L Abraham; Richard C Welch; Carlos G Vanoye; Lia Crotti; Marianne Arnestad; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Ashild Vege; Torleiv O Rognum; Dan Mark Roden; Peter J Schwartz; Alfred L George
Cardiac potassium channel dysfunction in sudden infant death syndrome.
Journal of molecular and cellular cardiology 2008;44(3):571-81.
2007: Lia Crotti; Chiara Ferrandi; Roberto Insolia; Matteo Pedrazzini; E Andreoli; Alessia Veia; Gabriele Crimi; A Agnetti; Gaetano M De Ferrari; Peter J Schwartz
Gene symbol: SCN5A.
Human genetics 2007;120(6):913.
2007: Lia Crotti; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; L Tosin; Cinzia Moncalvo; A Turco; A Agnetti; Gaetano M De Ferrari; Peter J Schwartz
Gene symbol: KCNQ1.
Human genetics 2007;120(6):912.
2007: Lia Crotti; Matteo Pedrazzini; Chiara Ferrandi; Roberto Insolia; L Tosin; Alessandro Vicentini; A Turco; Gaetano M De Ferrari; Peter J Schwartz
Gene symbol: KCNH2.
Human genetics 2007;120(6):912.
2007: Lia Crotti; Chiara Ferrandi; Roberto Insolia; Matteo Pedrazzini; L Tosin; Alessia Veia; A Turco; Gaetano M De Ferrari; Peter J Schwartz
Gene symbol: SCN5A.
Human genetics 2007;120(6):911-2.
2007: Dao W Wang; Reshma R Desai; Lia Crotti; Marianne Arnestad; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Ashild Vege; Torleiv O Rognum; Peter J Schwartz; Alfred L George
Cardiac sodium channel dysfunction in sudden infant death syndrome.
Circulation 2007;115(3):368-76.
2007: Marianne Arnestad; Lia Crotti; Torleiv O Rognum; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Ashild Vege; Dao W Wang; Troy E Rhodes; Alfred L George; Peter J Schwartz
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Circulation 2007;115(3):361-7.
2005: Lia Crotti; Andrew L Lundquist; Roberto Insolia; Matteo Pedrazzini; Chiara Ferrandi; Gaetano M De Ferrari; Alessandro Vicentini; Ping Yang; Dan Mark Roden; Alfred L George; Peter J Schwartz
KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome.
Circulation 2005;112(9):1251-8.