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Browsing by Author Spazzolini C

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Issue DateTitleAuthor(s)
2007The common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification.Crotti L; Spazzolini C; Schwartz Pj; Shimizu W; Denjoy I; Schulze bahr E; Zaklyazminskaya Ev; Swan H; Ackerman MJ; Moss AJ; Wilde AA; Horie M; Brink Pa; Insolia R; De Ferrari GM; Crimi G
2006Cost-effectiveness of neonatal ECG screening for the long QT syndromeQuaglini S; Rognoni C; Spazzolini C; Priori SG; Mannarino S; Schwartz PJ
2006The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcomeSchwartz PJ; Spazzolini C; Crotti L; Bathen J; Amlie JP; Timothy K; Shkolnikova M; Berul CI; Bitner Glindzicz M; Toivonen L; Horie M; Schulze Bahr E; Denjoy I
2004Left cardiac sympathetic denervation in the management of high-risk patients affected by the long-QT syndromeSchwartz PJ; Priori SG; Cerrone M; Spazzolini C; Odero A; Napolitano C; Bloise R; De Ferrari GM; Klersy C; Moss AJ; Zareba W; Robinson JL; Hall WJ; Brink PA; Toivonen L; Epstein AE; Li CL; Hu DY
2005Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder populationBrink PA; Crotti L; Corfield V; Goosen A; Durrheim G; Hedley P; Heradien M; Geldenhuys G; Vanoli E; Bacchini S; Spazzolini C; Lundquist AL; Roden DM; George AL; Schwartz PJ
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