VALLO, LAURA
VALLO, LAURA
A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2
2004-01-01 Bonifazi, E; Vallo, L; Giardina, E; Botta, A; Novelli, G
CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease
2004-03-01 Vavassori, P; Borgiani, P; Biancone, L; D'Apice, M; Blanco, G; Vallo, L; De Nigris, F; Monteleone, I; Monteleone, G; Pallone, F; Novelli, G
Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population
2005-02-01 Vallo, L; Bonifazi, E; Borgiani, P; Novelli, G; Botta, A
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2)
2006-03-01 Botta, A; Caldarola, S; Vallo, L; Bonifazi, E; Fruci, D; Gullotta, F; Massa, R; Novelli, G; Loreni, F
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population
2002-01-01 Borgiani, P; Vallo, L; D'Apice, Mr; Giardina, E; Pucci, S; Capon, F; Nistico', Sp; Chimenti, S; Pallone, F; Novelli, G
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients
2007-01-01 Salehi, L; Bonifazi, E; Stasio, E; Gennarelli, M; Botta, A; Vallo, L; Iraci, R; Massa, R; Antonini, G; Angelini, C; Novelli, G
Sistemi integrati di analisi molecolare per la diagnosi e lo studio delle malattie da triplette instabili
2005-01-01 Vallo, L
| Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
|---|---|---|---|---|
| 1-gen-2004 | A long PCR-based molecular protocol for detecting normal and expanded ZNF9 alleles in myotonic dystrophy type 2 | Bonifazi, E; Vallo, L; Giardina, E; Botta, A; Novelli, G | Articolo su rivista | |
| 1-mar-2004 | CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease | Vavassori, P; Borgiani, P; Biancone, L; D'Apice, M; Blanco, G; Vallo, L; De Nigris, F; Monteleone, I; Monteleone, G; Pallone, F; Novelli, G | Articolo su rivista | |
| 1-feb-2005 | Characterization of a single nucleotide polymorphism in the ZNF9 gene and analysis of association with myotonic dystrophy type II (DM2) in the Italian population | Vallo, L; Bonifazi, E; Borgiani, P; Novelli, G; Botta, A | Articolo su rivista | |
| 1-mar-2006 | Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) | Botta, A; Caldarola, S; Vallo, L; Bonifazi, E; Fruci, D; Gullotta, F; Massa, R; Novelli, G; Loreni, F | Articolo su rivista | |
| 1-gen-2002 | Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population | Borgiani, P; Vallo, L; D'Apice, Mr; Giardina, E; Pucci, S; Capon, F; Nistico', Sp; Chimenti, S; Pallone, F; Novelli, G | Articolo su rivista | |
| 1-gen-2007 | Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients | Salehi, L; Bonifazi, E; Stasio, E; Gennarelli, M; Botta, A; Vallo, L; Iraci, R; Massa, R; Antonini, G; Angelini, C; Novelli, G | Articolo su rivista | |
| 1-gen-2005 | Sistemi integrati di analisi molecolare per la diagnosi e lo studio delle malattie da triplette instabili | Vallo, L | Tesi di dottorato |