GIARDINA, EMILIANO
Dettaglio
GIARDINA, EMILIANO
Dipartimento di Biomedicina e prevenzione
Pubblicazioni
Risultati 1 - 20 di 112 (tempo di esecuzione: 0.001 secondi).
Data di pubblicazione | Titolo | Autore(i) | Tipo | File | |
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1 | 2014 | Absence of filaggrin mutation in a patient affected by pachyonychia congenita and mild atopic dermatitis | Terrinoni, A; Giardina, E; Pertusi, G; Cascella, R; Serra, V; Bornacina, C; Palombo, R; Tiberio, R; Gattoni, M; Novelli, G; Annicchiarico-Petruzzelli, M; Melino, G; Colombo, E | Articolo su rivista | - |
2 | 2014 | Age-related macular degeneration: insights into inflammatory genes | Cascella, R; Ragazzo, M; Strafella, C; Missiroli, F; Borgiani, P; Angelucci, F; Marsella, LT; Cusumano, A; Novelli, G; Ricci. F; Giardina, E | Articolo su rivista | Open Access |
3 | 2020 | Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications | Strafella, C; Caputo, V; Termine, A; Barati, S; Gambardella, S; Borgiani, P; Caltagirone, C; Novelli, G; Giardina, E; Cascella, R | Articolo su rivista | Open Access |
4 | 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 | Solo autorizzati |
5 | 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 | riservati |
6 | mag-2013 | Association of KIF3A, but not OVOL1 and ACTL9, with atopic eczema in Italian patients | Lepre, T; Cascella, R; Ragazzo, M; Galli, E; Novelli, G; Giardina, E | Articolo su rivista | - |
7 | 2003 | Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction. | Mango, R; Clementi, F; Borgiani, P; Forleo, GB; Federici, M; Contino, G; Giardina, E; Garza, L; Fahdi, IE; Lauro, R; Mehta, JL; Novelli, G; Romeo, F | Articolo su rivista | - |
8 | 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 | Open Access |
9 | lug-2019 | Bilateral Retinal Angiomatous Proliferation in a Variant of Retinitis Pigmentosa | Aloe, G; M De Sanctis, C; Strafella, C; Cascella, R; Missiroli, F; Cesareo, M; Giardina, E; Ricci, F | Articolo su rivista | - |
10 | 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 | riservati |
11 | 2018 | Can Tangier disease cause male infertility? A case report and an overview on genetic causes of male infertility and hormonal axis involved. | Stocchi, L; Giardina, E; Varriale, L; Sechi, A; Vagnini, A; Parri, G; Valentini, M; Capalbo, M | Articolo su rivista | - |
12 | nov-2004 | Characterization of the loricrin (LOR) gene as a positional candidate for the PSORS4 psoriasis susceptibility locus | Giardina, E; Capon, F; De Rosa, M; Mango, R; Zambruno, G; Orecchia, A; Chimenti, S; Giardina, B; Novelli, G | Articolo su rivista | - |
13 | apr-2014 | Clinical trial sponsors' refusal to communicate genetic research results to subjects | Porteri, C; Giardina, E; Eusebi, L | Articolo su rivista | - |
14 | 2006 | Co-localization of susceptibility loci for psoriasis (PSORS4) and atopic dermatitis (ATOD2) on human chromosome 1q21 | Giardina, E; Sinibaldi, C; Chini, L; Moschese, V; Marulli, G; Provini, A; Rossi, P; Paradisi, M; Chimenti, S; Galli, E; Brunetti, E; Girolomoni, G; Novelli, G | Articolo su rivista | riservati |
15 | 2020 | Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1) | Frezza, E; Fuccillo, E; Petrucci, A; Greco, G; Nucera, G; Bruno, E; Giardina, E; Tupler, R; Di Mauro, R; Di Girolamo, S; Massa, R | Articolo su rivista | riservati |
16 | 2014 | Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma | Giardina, E; Oddone, F; Lepre, T; Centofanti, M; Peconi, C; Tanga, L; Quaranta, L; Frezzotti, P; Novelli, G; Manni, G | Articolo su rivista | - |
17 | nov-2010 | Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis | Hüffmeier, U; Uebe, S; Ekici, AB; Bowes, J; Giardina, E; Korendowych, E; Juneblad, K; Apel, M; McManus, R; Ho, P; Bruce, IN; Ryan, AW; Behrens, F; Lascorz, J; Böhm, B; Traupe, H; Lohmann, J; Gieger, C; Wichmann, H; Herold, C; Steffens, M; Klareskog, L; Wienker, TF; Fitzgerald, O; Alenius, G; McHugh, NJ; Novelli, G; Burkhardt, H; Barton, A; Reis, A | Articolo su rivista | - |
18 | 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 | riservati |
19 | 2020 | Defective proteasome biogenesis into skin fibroblasts isolated from Rett syndrome subjects with MeCP2 non-sense mutations | Sbardella, D; Tundo, GR; Cunsolo, V; Grasso, G; Cascella, R; Caputo, V; Santoro, AM; Milardi, D; Pecorelli, A; Ciaccio, C; Di Pierro, D; Leoncini, S; Campagnolo, L; Pironi, V; Oddone, F; Manni, P; Foti, S; Giardina, E; De Felice, C; Hayek, J; Curatolo, P; Galasso, C; Valacchi, G; Coletta, M; GRAZIANI, G; Marini, S | Articolo su rivista | riservati |
20 | ago-2010 | Deletion of Late Cornified Envelope 3B and 3C genes is not associated with atopic dermatitis | Bergboer, J; Zeeuwen, P; Irvine, A; Weidinger, S; Giardina, E; Novelli, G; Den Heijer, M; Rodriguez, E; Illig, T; Riveira-Munoz, E; Campbell, L; Tyson, J; Dannhauser, E; O'Regan, G; Galli, E; Klopp, N; Koppelman, G; Novak, N; Estivill, X; McLean, W; Postma, D; Armour, J; Schalkwijk, J | Articolo su rivista | - |