VALECCE, ROSANNA
VALECCE, ROSANNA
A novel LMNA gene mutation in a multigenerational family with arrhythmogenic cardiac laminopathy
2015-01-01 Forleo, Cinzia; Carmosino, M.; Resta, Nicoletta; Rampazzo, A.; Valecce, Rosanna; Sorrentino, Sandro; Iacoviello, M.; Scardapane, Arnaldo; Simone, Cristiano; DE PASCALIS, Francesca; Sfrecola, MARIA ALESSANDRA; DE SANTIS, Delia; Musci, RITA LEONARDA; Marangelli, V.; Svelto, Maria; Favale, Stefano
Clinical and functional characterization of a novel mutation in lamin a/C gene in a multigenerational family with arrhythmogenic cardiac laminopathy
2015-01-01 Forleo, C.; Carmosino, M.; Resta, N.; Rampazzo, A.; Valecce, R.; Sorrentino, S.; Iacoviello, M.; Pisani, F.; Procino, G.; Gerbino, A.; Scardapane, A.; Simone, C.; Calore, M.; Torretta, S.; Svelto, M.; Favale, S.
Sarcomere gene mutations and clinical correlates in patients with hypertrophic cardiomyopathy
2015-01-01 DE SANTIS, Delia; Forleo, Cinzia; Marangelli, V.; Parodi, M. I.; Sorrentino, Sandro; Valecce, Rosanna; Iacoviello, M.; Sfrecola, MARIA ALESSANDRA; DE PASCALIS, Francesca; Musci, RITA LEONARDA; Pinto, Mariangela; Cecconi, M.; Coviello, D.; Favale, Stefano
Screening For Sarcomere Protein Gene Mutations and Genotype-Phenotype Correlations in Patients with Hypertrophic Cardiomyopathy: experience of a Single Centre
2014-01-01 Sfrecola, Alessandra; Forleo, Cinzia; Valecce, Rosanna; Sorrentino, Sandro; Iacoviello, Massimo; Pascalis, Francesca De; Parodi, Maria Isola; Cecconi, Massimiliano; Davì, Sabrina; Marangelli, Vito; Spirito, Paolo; Favale, Stefano
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A novel LMNA gene mutation in a multigenerational family with arrhythmogenic cardiac laminopathy | 1-gen-2015 | Forleo, Cinzia; Carmosino, M.; Resta, Nicoletta; Rampazzo, A.; Valecce, Rosanna; Sorrentino, Sandro; Iacoviello, M.; Scardapane, Arnaldo; Simone, Cristiano; DE PASCALIS, Francesca; Sfrecola, MARIA ALESSANDRA; DE SANTIS, Delia; Musci, RITA LEONARDA; Marangelli, V.; Svelto, Maria; Favale, Stefano | |
| Clinical and functional characterization of a novel mutation in lamin a/C gene in a multigenerational family with arrhythmogenic cardiac laminopathy | 1-gen-2015 | Forleo, C.; Carmosino, M.; Resta, N.; Rampazzo, A.; Valecce, R.; Sorrentino, S.; Iacoviello, M.; Pisani, F.; Procino, G.; Gerbino, A.; Scardapane, A.; Simone, C.; Calore, M.; Torretta, S.; Svelto, M.; Favale, S. | |
| Sarcomere gene mutations and clinical correlates in patients with hypertrophic cardiomyopathy | 1-gen-2015 | DE SANTIS, Delia; Forleo, Cinzia; Marangelli, V.; Parodi, M. I.; Sorrentino, Sandro; Valecce, Rosanna; Iacoviello, M.; Sfrecola, MARIA ALESSANDRA; DE PASCALIS, Francesca; Musci, RITA LEONARDA; Pinto, Mariangela; Cecconi, M.; Coviello, D.; Favale, Stefano | |
| Screening For Sarcomere Protein Gene Mutations and Genotype-Phenotype Correlations in Patients with Hypertrophic Cardiomyopathy: experience of a Single Centre | 1-gen-2014 | Sfrecola, Alessandra; Forleo, Cinzia; Valecce, Rosanna; Sorrentino, Sandro; Iacoviello, Massimo; Pascalis, Francesca De; Parodi, Maria Isola; Cecconi, Massimiliano; Davì, Sabrina; Marangelli, Vito; Spirito, Paolo; Favale, Stefano |