Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Valentina D'Andria"'
Publikováno v:
Cardiologia Ambulatoriale. :191-202
Autor:
Andrea Passantino, Valentina D’Andria
Publikováno v:
Cardiologia Ambulatoriale. :57-66
Autor:
Pietro Guida, Stefano Favale, Marco Matteo Ciccone, Cinzia Forleo, Massimo Iacoviello, Mariligia Panunzio, Sandro Sorrentino, Valentina D'Andria
Publikováno v:
Clinical Autonomic Research. 20:167-173
Nitrate-stimulated head-up tilt testing (HUT) is currently recommended to confirm the diagnosis of vasovagal syncope in subjects with syncope of unknown origin. Given the few data currently available, the aim of this study was to assess correlations
Autor:
Valentina D'Andria, Pietro Guida, Massimo Iacoviello, Sandro Sorrentino, Stefano Favale, Luciana D'Alonzo, Marica Rodio, Cinzia Forleo
Publikováno v:
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology. 12(8)
The involvement of arterial baroreflex function in the pathophysiology of vasovagal syncope (VVS) is controversial, and there are no published data supporting its clinical usefulness. The aim of this study was to evaluate the role of arterial baroref
Autor:
Valentina D'Andria, Massimo Iacoviello, Cinzia Forleo, Sandro Sorrentino, Pietro Guida, Stefano Favale
Publikováno v:
Autonomic neuroscience : basicclinical. 155(1-2)
Although the pathophysiology of vasovagal syncope is not completely understood, the involvement of sympathetic nervous system alterations has been suggested. Since predisposition to fainting during orthostatic challenge may be associated with genetic
Autor:
Pietro Guida, Valentina D'Andria, Cinzia Forleo, Stefano Favale, Sandro Sorrentino, Massimo Iacoviello
Publikováno v:
Clinical autonomic research : official journal of the Clinical Autonomic Research Society. 19(6)
Genetics may be involved in the pathophysiology of vasovagal syncope. The 3A/4A polymorphism of the EDN1 gene affects the expression of endothelin-1, and the H323H T/C polymorphism of the EDNRA gene encoding for the endothelin type A receptor has bee