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Mostrati risultati da 21 a 40 di 251
Data di pubblicazione Titolo Autore(i) File
1-gen-2012 Blood presence of circulating oncofetal fibronectin mRNA, by RT-PCR, does not represent a useful specific marker for the management and follow-up of thyroid cancer patients Vendittelli, F; Raffaelli, Marco; Fadda, Guido; Carelli Alinovi, Cristiana; Paolillo, C; Bellantone, Rocco Domenico Alfonso; Zuppi, C; Capoluongo, E.
1-gen-2007 Body cell mass measured by bioelectrical impedance spectroscopy in professional football (soccer) players. Calla', Cinzia Anna Maria
1-gen-2019 Brain mitochondrial proteome alteration driven by creatine deficiency suggests novel therapeutic venues for creatine deficiency syndromes Giusti, L; Molinaro, A; Alessandri, Mg; Boldrini, C; Ciregia, F; Lacerenza, S; Ronci, M; Urbani, Andrea; Cioni, G; Mazzoni, Mr; Pizzorusso, T; Lucacchini, A; Baroncelli, L
1-gen-2017 BRCA mutational status, initial disease presentation, and clinical outcome in high-grade serous advanced ovarian cancer: a multicenter study Petrillo, Marco; Marchetti, Claudia; De Leo, R; Musella, A; Capoluongo, Ettore Domenico; Paris, Ida; Panici, Pb; Scambia, Giovanni; Fagotti, Anna
1-gen-2016 BRCA to the future: towards best testing practice in the era of personalised healthcare Capoluongo, Ettore Domenico
1-gen-2015 CA 19-9: Biochemical and Clinical Aspects Scara', Salvatore; Bottoni, Patrizia; Scatena, Roberto
1-gen-2015 CA 19-9: Biochemical and Clinical Aspects Scara', Salvatore; Bottoni, Patrizia; Scatena, Roberto
1-gen-2015 CA 19-9: Biochemical and Clinical Aspects Scara', Salvatore; Bottoni, Patrizia; Scatena, Roberto
1-gen-2015 Cancer Biomarkers: A Status Quo Scatena, Roberto
1-gen-2016 Chanarin Dorfman Syndrome: A Case Report with Novel Nonsense Mutation Gupta, N.; Gothwal, S.; Satpathy, A. K.; Missaglia, Sara; Tavian, Daniela; Das, P.; Timila, D.; Kabra, M.
1-gen-2017 Characterization of a new BRCA1 rearrangement in an Italian woman with hereditary breast and ovarian cancer syndrome Concolino, P; Rizza, Roberta; Hackmann, K; Paris, Ida; Minucci, Angelo; De Paolis, Elisa; Scambia, Giovanni; Zuppi, Cecilia; Schrock, E; Capoluongo, Ettore Domenico
1-gen-2002 Chronic taaurine supplementation ameliorates oxidative stress and Na+ K+ ATPase impairment in the retina of diabetic rats Di Leo, Mauro; Santini, Stefano Angelo; Cicerone, S; Lepore, Domenico; Gentiloni Silveri, Nicolo'; Caputo, Salvatore; Greco, Aldo Virgilio; Giardina, Bruno; Franconi, F; Ghirlanda, Giovanni
1-gen-2022 Circulating and Salivary NGF and BDNF Levels in SARS-CoV-2 Infection: Potential Predictor Biomarkers of COVID-19 Disease-Preliminary Data Biamonte, Filippo; Re, Agnese; Balzamino, Bijorn Omar; Ciasca, Gabriele; Santucci, Daniela; Napodano, Cecilia; Nocca, Giuseppina; Fiorita, Antonella; Marino, Mariapaola; Basile, Umberto; Micera, Alessandra; Calla', Cinzia Anna Maria
1-gen-2014 Circulating fetal cell-free DNA and prenatal molecular diagnostics: are we ready for consensus? Capoluongo, Ettore Domenico; Plebani, M.
1-gen-2013 Circulating tumor cells in colorectal cancer patients Torino, F; Bonmassar, E; Bonmassar, L; De, ; Barnabei, A; Zuppi, Cecilia; Capoluongo, Ettore Domenico; Aquino, A.
1-gen-2013 Circulating tumour cells and cancer stem cells: A role for proteomics in defining the interrelationships between function,phenotype and differentiation with potential clinical applications. Scatena, Roberto; Bottoni, Patrizia; Giardina, Bruno
1-gen-2013 Clinical and biological role of secretory phospholipase A2 in acute respiratory distress syndrome infants De Luca, Daniele; Lopez Rodriguez, E; Minucci, Angelo; Vendittelli, Francesca; Gentile, Leonarda; Stival, Eleonora; Conti, Giorgio; Piastra, Marco; Antonelli, Massimo; Echaide, M; Perez Gil, J; Capoluongo, Ettore Domenico
1-gen-2015 Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome Minucci, Angelo; Ruggiero, Antonio; Canu, Giulia; Maurizi, Palma; De Bonis, Maria; Concolino, Paola; De Luca, Daniele; Capoluongo, Ettore Domenico
1-gen-2014 Comments to ``A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency{''} Concolino, Paola; Mello Dottoressa, Enrica; Rossodivita, Aurora Natalia; Giardina, Bruno; Capoluongo, Ettore Domenico
1-gen-2020 Comparative computational analysis of SARS-CoV-2 nucleocapsid protein epitopes in taxonomically related coronaviruses Tilocca, B; Soggiu, A; Sanguinetti, Maurizio; Musella, V; Britti, D; Bonizzi, L; Urbani, Andrea; Roncada, Paola
Mostrati risultati da 21 a 40 di 251
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