DSpace ISS DSpace ISS DSpace ISS
 

DSpace ISS >

Browsing by Author Crotti L

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:   
Sort by: In order: Results/Page Authors/Record:
Showing results 1 to 14 of 14
Issue DateTitleAuthor(s)
2007Can a message from the dead save lives?Schwartz Pj; Crotti L
2007Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death SyndromeSchwartz Pj; Crotti L
2007Cardiac sodium channel dysfunction in sudden infant death syndromeWang DW; Desai RR; Crotti L; Arnestad M; Insolia R; Pedrazzini M; Ferrandi C; Vege A; Rognum T; Schwartz PJ; George AL
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
2006Does pregnancy increase cardiac risk for LQT1 patients?Heradien MJ; Goosen A; Crotti L; Durrheim G; Corfield V; Brink PA; Schwartz PJ
2007Gene symbol: KCNH2 in Gilles de la Tourette syndromeCrotti L; Pedrazzini M; Ferrandi C; Insolia R; Tosin L; Vicentini A; Turco A; De Ferrari GM; Schwartz PJ
2007Gene symbol: KCNH2 in prolongation of the QTcCrotti L; Insolia R; Pedrazzini M; Andreoli C; Gabanti E; Moncalvo C; Crimi G; De Ferrari GM; Schwartz PJ
2007Gene symbol: KCNQ1 in QTc prolongationCrotti L; Insolia R; Pedrazzini M; Ferrandi C; Tosin L; Moncalvo C; Turco A; Agnetti A; De Ferrari GM; Schwartz PJ
2007Gene symbol: SCN5A in Long QT syndromeCrotti L; Ferrandi C; Insolia R; Pedrazzini M; Andreoli E; Veia A; Crimi G; Agnetti A; De Ferrari GM; Schwartz PJ
2007Gene symbol: SCN5A in Long QT syndrome (LQTS)Crotti L; Ferrandi C; Insolia R; Pedrazzini M; Tosin L; Veia A; Turco A; Deferrari GM; 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
2005KCNH2-K897T is a genetic modifier of latent congenital long-QT SYNDROMECrotti L; Lundquist AL; Insolia R; Pedrazzini M; Ferrandi C; De Ferrari GM; Vicentini A; Yang P; Roden DM; George AL Jr; Schwartz PJ
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
2007Prevalence of long-QT syndrome gene variants in sudden infant death syndromeArnestad M; Crotti L; Rognum TO; Insolia R; Pedrazzini M; Ferrandi C; Vege A; Wang DW; Rhodes TE; George AL; Schwartz PJ
Showing results 1 to 14 of 14

 

Valid XHTML 1.0! DSpace ISS  Istituto Superiore di Sanità  - Feedback