CROTTI, LIA

CROTTI, LIA  

DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)  

Mostra records
Risultati 1 - 20 di 230 (tempo di esecuzione: 0.028 secondi).
Titolo Tipologia Data di pubblicazione Autori File
Brugada and Long QT Syndrome are two different diseases: True or False? 03 - Contributo in libro 1999 Crotti, L +
Idiopathic Ventricular Fibrillation 01 - Articolo su rivista 1999 Crotti, L +
Idiopathic Ventricular Fibrillation 03 - Contributo in libro 2000 Crotti, L +
The elusive link between LQT3 and Brugada syndrome: the role of flecainide challenge 01 - Articolo su rivista 2000 Crotti, L +
Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families 01 - Articolo su rivista 2000 Crotti L +
Long QT Syndrome and Brugada Syndrome : 2 aspects of the same disease? 01 - Articolo su rivista 2001 Crotti L +
The Long QT Syndrome 01 - Articolo su rivista 2001 Crotti, L +
The ICD for the long QT syndrome: which indications, complications, and results? 03 - Contributo in libro 2005 Crotti L +
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population 01 - Articolo su rivista 2005 CROTTI, LIA +
KCNH2-K897T Is a Genetic Modifier of Latent Congenital Long-QT Syndrome 01 - Articolo su rivista 2005 Crotti L +
The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome 01 - Articolo su rivista 2006 Crotti L +
Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation? 01 - Articolo su rivista 2006 Crotti L +
Gene symbol: SCN5A. Disease: Long QT syndrome in Novel human pathological mutations 01 - Articolo su rivista 2007 Crotti Lia +
Gene symbol: KCNQ1. Disease: Long QT syndrome 01 - Articolo su rivista 2007 Crotti Lia +
Cardiac arrhythmias of genetic origin are important contributors to Sudden Infant Death Syndrome 01 - Articolo su rivista 2007 Crotti, L +
Gene symbol: SCN5A. Disease: Long QT syndrome in Novel human pathological mutations 01 - Articolo su rivista 2007 Crotti, Lia +
Prevalence of long-QT syndrome gene variants in sudden infant death syndrome 01 - Articolo su rivista 2007 Crotti, L +
The Common Long QT Syndrome mutation KCNQ1/A341V causes unusually severe clinical manifestations in patients with different ethnic backgrounds: toward a mutation-specific risk stratification 01 - Articolo su rivista 2007 Crotti L. +
Gene symbol: KCNH2. Disease: Long QT syndrome in Novel human pathological mutations 01 - Articolo su rivista 2007 Crotti Lia +
Cardiac sodium channel dysfunction in sudden infant death syndrome 01 - Articolo su rivista 2007 Crotti L +