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Browsing by Author Denjoy I

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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
2007The Jervell and Lange-Nielsen syndrome Natural history, molecular basis and clinical outcomeDenjoy I; Lupoglazoff JM; Villain E; Vaksmann G; Godart F; Lucet V; Leenhard A; Guicheney P; 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
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