Sfoglia per Autore
FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation
2015-01-01 Cascella, R; Strafella, C; Germani, C; Manzo, L; Marsella, Lt; Borgiani, P; Sobhy, N; Abdelmaksood, R; Gerou, S; Ioannides, D; Sangiuolo, Fc; Novelli, G; Hashad, D; Vakirlis, E; Giardina, E
Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01
2015-01-01 Cascella, R; Strafella, C; Ragazzo, M; Zampatti, S; Borgiani, P; Gambardella, S; Pirazzoli, A; Novelli, G; Giardina, E
Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing
2015-01-01 Cascella, R; Stocchi, L; Strafella, C; Mezzaroma, I; Mannazzu, M; Vullo, V; Montella, F; Parruti, G; Borgiani, P; Sangiuolo, Fc; Novelli, G; Pirazzoli, A; Zampatti, S; Giardina, E
Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis
2016-01-01 Cascella, R; Strafella, C; Longo, G; Maccarone, M; Borgiani, P; Sangiuolo, Fc; Novelli, G; Giardina, E
Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry
2016-01-01 Pietropolli, A; Capogna, M; Cascella, R; Germani, C; Bruno, V; Strafella, C; Sarta, S; Ticconi, C; Marmo, G; Gallaro, S; Longo, G; Marsella, Lt; Novelli, A; Novelli, G; Piccione, E; Giardina, E
KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility
2017-01-01 Cascella, R; Strafella, C; Ragazzo, M; Manzo, L; Costanza, G; Bowes, J; Hüffmeier, U; Potenza, S; Sangiuolo, Fc; Reis, A; Barton, A; Novelli, G; Orlandi, A; Giardina, E
Gender and complex diseases: Insights into sex-specific epigenetic|Genere e malattie complesse: Meccanismi epigenetici sesso-specifici
2018-01-01 Caputo, V; Cascella, R; Strafella, C; Giardina, E; Novelli, G
Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD
2018-01-01 Cascella, R; Strafella, C; Caputo, V; Galota, Rm; Errichiello, V; Scutifero, M; Petillo, R; Marella, Gl; Arcangeli, M; Colantoni, L; Zampatti, S; Ricci, E; Deidda, G; Politano, L; Giardina, E
Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis
2018-01-01 Zampatti, S; Mela, J; Peconi, C; Pagliaroli, G; Carboni, S; Barrano, G; Zito, I; Cascella, R; Marella, G; Milano, F; Arcangeli, M; Caltagirone, C; Novelli, A; Giardina, E
Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants
2018-01-01 Cascella, R; Strafella, C; Longo, G; Ragazzo, M; Manzo, L; De Felici, C; Errichiello, V; Caputo, V; Viola, F; Eandi, Cm; Staurenghi, G; Cusumano, A; Mauriello, S; Marsella, Lt; Ciccacci, C; Borgiani, P; Sangiuolo, F; Novelli, G; Ricci, F; Giardina, E
Application of precision medicine in neurodegenerative diseases
2018-01-01 Strafella, C; Caputo, V; Galota, Mr; Zampatti, S; Marella, G; Mauriello, S; Cascella, R; Giardina, E
Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents.
2018-01-01 Bianchi, L; Costanza, G; Campione, E; Ruzzetti, M; DI STEFANI, A; Diluvio, L; Giardina, E; Cascella, R; Cordiali Fei, P; Bonifati, C; Chiricozzi, A; Novelli, G; Ensoli, F; Orlandi, A
Assessing individual risk for AMD with genetic counseling, family history, and genetic testing
2018-01-01 Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, Lt; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E
Expression and potential role of cellular retinol binding protein I in psoriasis
2018-12-04 Costanza, G; Doldo, E; Ferlosio, A; Tarquini, C; Passeri, D; Cascella, R; Bavetta, M; Di Stefani, A; Bonifati, C; Agostinelli, S; Centofanti, F; Giardina, E; Campione, E; Bianchi, L; Donati, P; Morrone, A; Orlandi, A
The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A.
2019-01-01 Strafella, C; Errichiello, V; Caputo, V; Aloe, G; Ricci, F; Cusumano, A; Novelli, G; Giardina, E; Cascella, R
Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era.
2019-01-01 Zampatti, S; Colantoni, L; Strafella, C; Galota, R; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E
Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report.
2019-01-01 Cusumano, A; Falsini, B; Giardina, E; Cascella, R; Sebastiani, J; Marshall, J
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report.
2019-01-01 Strafella, C; Campoli, G; Galota, R; Caputo, V; Pagliaroli, G; Carboni, S; Zampatti, S; Peconi, C; Mela, J; Sancricca, C; Primiano, G; Minozzi, G; Servidei, S; Cascella, R; Giardina, E
Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis
2019-01-01 Musumeci, Ml; Fiorentini, F; Bianchi, L; Cascella, R; Giardina, E; Caputo, V; Micali, G
Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations.
2019-06-04 Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E
Data di pubblicazione | Titolo | Autore(i) | Tipo | File |
---|---|---|---|---|
1-gen-2015 | FLG (filaggrin) null mutations and sunlight exposure: Evidence of a correlation | Cascella, R; Strafella, C; Germani, C; Manzo, L; Marsella, Lt; Borgiani, P; Sobhy, N; Abdelmaksood, R; Gerou, S; Ioannides, D; Sangiuolo, Fc; Novelli, G; Hashad, D; Vakirlis, E; Giardina, E | Articolo su rivista | |
1-gen-2015 | Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01 | Cascella, R; Strafella, C; Ragazzo, M; Zampatti, S; Borgiani, P; Gambardella, S; Pirazzoli, A; Novelli, G; Giardina, E | Articolo su rivista | |
1-gen-2015 | Comparative analysis between saliva and buccal swabs as source of DNA: Lesson from HLA-B∗57:01 testing | Cascella, R; Stocchi, L; Strafella, C; Mezzaroma, I; Mannazzu, M; Vullo, V; Montella, F; Parruti, G; Borgiani, P; Sangiuolo, Fc; Novelli, G; Pirazzoli, A; Zampatti, S; Giardina, E | Articolo su rivista | |
1-gen-2016 | Pharmacogenomics of multifactorial diseases: A focus on psoriatic arthritis | Cascella, R; Strafella, C; Longo, G; Maccarone, M; Borgiani, P; Sangiuolo, Fc; Novelli, G; Giardina, E | Articolo su rivista | |
1-gen-2016 | Three-hour analysis of non-invasive foetal sex determination: application of Plexor chemistry | Pietropolli, A; Capogna, M; Cascella, R; Germani, C; Bruno, V; Strafella, C; Sarta, S; Ticconi, C; Marmo, G; Gallaro, S; Longo, G; Marsella, Lt; Novelli, A; Novelli, G; Piccione, E; Giardina, E | Articolo su rivista | |
1-gen-2017 | KIF3A and IL-4 are disease-specific biomarkers for psoriatic arthritis susceptibility | Cascella, R; Strafella, C; Ragazzo, M; Manzo, L; Costanza, G; Bowes, J; Hüffmeier, U; Potenza, S; Sangiuolo, Fc; Reis, A; Barton, A; Novelli, G; Orlandi, A; Giardina, E | Articolo su rivista | |
1-gen-2018 | Gender and complex diseases: Insights into sex-specific epigenetic|Genere e malattie complesse: Meccanismi epigenetici sesso-specifici | Caputo, V; Cascella, R; Strafella, C; Giardina, E; Novelli, G | Articolo su rivista | |
1-gen-2018 | Digenic inheritance of shortened repeat units of the D4Z4 region and a loss-of-function variant in SMCHD1 in a Family with FSHD | Cascella, R; Strafella, C; Caputo, V; Galota, Rm; Errichiello, V; Scutifero, M; Petillo, R; Marella, Gl; Arcangeli, M; Colantoni, L; Zampatti, S; Ricci, E; Deidda, G; Politano, L; Giardina, E | Articolo su rivista | |
1-gen-2018 | Identification of Duchenne/Becker muscular dystrophy mosaic carriers through a combined DNA/RNA analysis | Zampatti, S; Mela, J; Peconi, C; Pagliaroli, G; Carboni, S; Barrano, G; Zito, I; Cascella, R; Marella, G; Milano, F; Arcangeli, M; Caltagirone, C; Novelli, A; Giardina, E | Articolo su rivista | |
1-gen-2018 | Uncovering genetic and non-genetic biomarkers specific for exudative age-related macular degeneration: Significant association of twelve variants | Cascella, R; Strafella, C; Longo, G; Ragazzo, M; Manzo, L; De Felici, C; Errichiello, V; Caputo, V; Viola, F; Eandi, Cm; Staurenghi, G; Cusumano, A; Mauriello, S; Marsella, Lt; Ciccacci, C; Borgiani, P; Sangiuolo, F; Novelli, G; Ricci, F; Giardina, E | Articolo su rivista | |
1-gen-2018 | Application of precision medicine in neurodegenerative diseases | Strafella, C; Caputo, V; Galota, Mr; Zampatti, S; Marella, G; Mauriello, S; Cascella, R; Giardina, E | Articolo su rivista | |
1-gen-2018 | Biomolecular index of therapeutic efficacy in psoriasis treated by anti-TNF alpha agents. | Bianchi, L; Costanza, G; Campione, E; Ruzzetti, M; DI STEFANI, A; Diluvio, L; Giardina, E; Cascella, R; Cordiali Fei, P; Bonifati, C; Chiricozzi, A; Novelli, G; Ensoli, F; Orlandi, A | Articolo su rivista | |
1-gen-2018 | Assessing individual risk for AMD with genetic counseling, family history, and genetic testing | Cascella, R; Strafella, C; Longo, G; Manzo, L; Ragazzo, M; De Felici, C; Gambardella, S; Marsella, Lt; Novelli, G; Borgiani, P; Sangiuolo, F; Cusumano, A; Ricci, F; Giardina, E | Articolo su rivista | |
4-dic-2018 | Expression and potential role of cellular retinol binding protein I in psoriasis | Costanza, G; Doldo, E; Ferlosio, A; Tarquini, C; Passeri, D; Cascella, R; Bavetta, M; Di Stefani, A; Bonifati, C; Agostinelli, S; Centofanti, F; Giardina, E; Campione, E; Bianchi, L; Donati, P; Morrone, A; Orlandi, A | Articolo su rivista | |
1-gen-2019 | The Interplay between miRNA-Related Variants and Age-Related Macular Degeneration: EVIDENCE of Association of MIR146A and MIR27A. | Strafella, C; Errichiello, V; Caputo, V; Aloe, G; Ricci, F; Cusumano, A; Novelli, G; Giardina, E; Cascella, R | Articolo su rivista | |
1-gen-2019 | Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. | Zampatti, S; Colantoni, L; Strafella, C; Galota, R; Caputo, V; Campoli, G; Pagliaroli, G; Carboni, S; Mela, J; Peconi, C; Gambardella, S; Cascella, R; Giardina, E | Articolo su rivista | |
1-gen-2019 | Doyne honeycomb retinal dystrophy - functional improvement following subthreshold nanopulse laser treatment: a case report. | Cusumano, A; Falsini, B; Giardina, E; Cascella, R; Sebastiani, J; Marshall, J | Articolo su rivista | |
1-gen-2019 | Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. | Strafella, C; Campoli, G; Galota, R; Caputo, V; Pagliaroli, G; Carboni, S; Zampatti, S; Peconi, C; Mela, J; Sancricca, C; Primiano, G; Minozzi, G; Servidei, S; Cascella, R; Giardina, E | Articolo su rivista | |
1-gen-2019 | Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis | Musumeci, Ml; Fiorentini, F; Bianchi, L; Cascella, R; Giardina, E; Caputo, V; Micali, G | Articolo su rivista | |
4-giu-2019 | Atopic Eczema: Genetic Analysis of COL6A5, COL8A1, and COL10A1 in Mediterranean Populations. | Strafella, C; Caputo, V; Minozzi, G; Milano, F; Arcangeli, M; Sobhy, N; Abdelmaksood, R; Hashad, D; Vakirlis, E; Novelli, G; Cascella, R; Giardina, E | Articolo su rivista |
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile