GIARDINA, EMILIANO

GIARDINA, EMILIANO  

Dipartimento di Biomedicina e prevenzione  

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Risultati 1 - 20 di 134 (tempo di esecuzione: 0.038 secondi).
Data di pubblicazione Titolo Autore(i) Tipo File
1-gen-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
1-gen-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
1-gen-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
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 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
1-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
1-gen-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, G; Federici, M; Contino, G; Giardina, E; Garza, L; Fahdi, I; Lauro, R; Mehta, J; Novelli, G; Romeo, F 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
10-feb-2022 The BDNF Val66Met Polymorphism (rs6265) Modulates Inflammation and Neurodegeneration in the Early Phases of Multiple Sclerosis Dolcetti, E; Bruno, A; Azzolini, F; Gilio, L; Moscatelli, A; De Vito, F; Pavone, L; Iezzi, E; Gambardella, S; Giardina, E; Ferese, R; Buttari, F; Rizzo, Fr; Furlan, R; Finardi, A; Musella, A; Mandolesi, G; Guadalupi, L; Centonze, D; Stampanoni Bassi, M Articolo su rivista
1-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
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 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
1-giu-2021 Case report: Sars-CoV-2 infection in a vaccinated individual: evaluation of the immunological profile and virus transmission risk Strafella, C; Caputo, V; Guerrera, G; Termine, A; Fabrizio, C; Cascella, R; Picozza, M; Caltagirone, C; Rossini, A; Balice, Mp; Salvia, A; Battistini, L; Borsellino, G; Giardina, E Articolo su rivista
1-ago-2021 Characterization of a natural variant of human NDP52 and its functional consequences on mitophagy Di Rita, A; Angelini, D; Maiorino, T; Caputo, V; Cascella, R; Kumar, M; Tiberti, M; Lambrughi, M; Wesch, N; Löhr, F; Dötsch, V; Carinci, M; D'Acunzo, P; Chiurchiù, V; Papaleo, E; Rogov, V; Giardina, E; Battistini, L; Strappazzon, F Articolo su rivista
1-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
1-apr-2014 Clinical trial sponsors' refusal to communicate genetic research results to subjects Porteri, C; Giardina, E; Eusebi, L Articolo su rivista
1-gen-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
1-gen-2021 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
1-lug-2021 Cohort analysis of 67 Charcot-Marie-Tooth Italian patients: identification of new mutations and broadening of phenotype expression produced by rare variants Ferese, R; Campopiano, R; Scala, S; D'Alessio, C; Storto, M; Buttari, F; Centonze, D; Logroscino, G; Zecca, C; Zampatti, S; Fornai, F; Cianci, V; Manfroi, E; Giardina, E; Magnani, M; Suppa, A; Novelli, G; Gambardella, S Articolo su rivista
1-gen-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