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Mostrati risultati da 157 a 176 di 254
Data di pubblicazione Titolo Autore(i) File
1-gen-2020 Molecular basis of COVID-19 relationships in different species: a one health perspective Tilocca, B; Soggiu, A; Musella, V; Britti, D; Sanguinetti, Maurizio; Urbani, Andrea; Roncada, Paola
1-gen-2019 Molecular basis of favism triggered by ingestion of frozen pumpkin cross-contaminated with fava beans Minucci, Angelo; Onori, Me; Mazzuccato, G; Urbani, Andrea; Capoluongo, E
1-gen-2010 Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutations Concolino, Paola; Mello Dottoressa, Enrica; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2017 Multicenter evaluation of an enzymatic method for glycated albumin Paleari, R; Bonetti, G; Calla', Cinzia Anna Maria; Carta, M; Ceriotti, F; Di Gaetano, N; Ferri, M; Guerra, E; Lavalle, G; Cascio, Cl; Martino, Fg; Montagnana, M; Moretti, M; Santini, G; Scribano, Donata; Testa, R; Vero, A; Mosca, A.
1-gen-2017 Multicenter evaluation of the new immunoassay method for TSH measurement using the automated DxI platform Dittadi, R.; Rizzardi, S.; Masotti, S.; Prontera, C.; Ripoli, A.; Fortunato, A.; Alfano, A.; Carrozza, C.; Correale, M.; Gessoni, G.; Migliardi, M.; Zucchelli, G.; Clerico, A.
1-gen-2016 Multidisciplinary team for elucidation of any new mutation and how this approach can be useful to individualize any genetic result: the case of BRCA2 c.631G > A/c.7008-2A > T genotype Minucci, Angelo; De Bonis, Maria; Costella, Alessandra; Scambia, Giovanni; Scandurra, Giuseppa; Capoluongo, Ettore Domenico
1-gen-2016 Multiple endocrine neoplasia type 1 (MEN1): An update of 208 new germline variants reported in the last nine years Concolino, Paola; Costella, Alessandra; Capoluongo, Ettore Domenico
1-gen-2009 Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report. Concolino, Paola; Mello, Enrica; Toscano, V; Ameglio, F; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2011 Multiplex Ligation-Dependent Probe Amplification Analysis Is Useful for Diagnosing Congenital Adrenal Hyperplasia but Requires a Deep Knowledge of CYP21A2 Genetics Concolino, Paola; Mello, E; Minucci, Angelo; Zuppi, Cecilia; Capoluongo, Ettore Domenico
1-gen-2015 Neuron-Specific Enolase as a Biomarker: Biochemical and Clinical Aspects Isgro', Maria Antonietta; Bottoni, Patrizia; Scatena, Roberto
1-gen-2009 A new splicing site mutation of the ABCB4 gene in intrahepatic cholestasis of pregnancy with raised serum gamma-GT Tavian, Daniela; Degiorgio, D.; Roncaglia, N.; Vergani, P.; Cameroni, I.; Colombo, Roberto; Coviello, D. A.
1-gen-2018 Non-catalytic region of tyrosine kinase adaptor protein 2 (NCK2) pathways as factor promoting aggressiveness in ovarian cancer Fanelli, Mara; Camperchioli, Alessia; Petrella, Lella; Petrillo, Marco; Baranello, Cinzia; Baccaro, Pina; Paolillo, Carmela; Capoluongo, Ettore Domenico; Scambia, Giovanni
1-gen-2017 A Noninvasive Surfactant Adsorption Test Predicting the Need for Surfactant Therapy in Preterm Infants Treated with Continuous Positive Airway Pressure Autilio, C; Echaide, M; Benachi, A; Marfaing-Koka, A; Capoluongo, Ed; Perez-Gil, J; De Luca, D.
1-gen-2013 Nonsteroidal Anti-Inflammatory Drug (NSAID) Use and Sarcopenia in Older People: Results From the ilSIRENTE Study Landi, Francesco; Marzetti, Emanuele; Liperoti, Rosa; Pahor, M; Russo, Andrea; Martone, Anna Maria; Colloca, Giuseppe Ferdinando; Capoluongo, Ettore Domenico; Bernabei, Roberto
1-gen-2019 Novel BRCA1 Large Genomic Rearrangements in Italian Breast/Ovarian Cancer Patients Rizza, R; Hackmann, K; Paris, I; Minucci, A; De Leo, R; Schrock, E; Urbani, A; Capoluongo, E; Gelli, G; Concolino, P
1-gen-2017 A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass (vol 45, pg 291, 2016) Ferraro, Pm; Minucci, A; Primiano, A; De Paolis, E; Gervasoni, J; Persichilli, S; Naticchia, A; Capoluongo, E; Gambaro, G
1-gen-2018 A novel CYP24A1 genotype associated to a clinical picture of hypercalcemia, nephrolithiasis and low bone mass Ferraro, Pietro Manuel; Minucci, Angelo; Primiano, Aniello; De Paolis, Elisa; Gervasoni, Jacopo; Persichilli, Silvia; Naticchia, Alessandro; Capoluongo, Ettore Domenico; Gambaro, Giovanni
1-gen-2010 Novel human pathological mutations. Gene symbol: UROD. Disease: porphyria, cutanea tarda Savino, M; Garrubba, M; Zelante, L; Aucella, F; Guida, Cc; Santini, Stefano Angelo
1-gen-2011 Novel strategies for tracing the exposure of meat cattle to illegal growth-promoters Nebbia, C; Urbani, Andrea; Carletti, M; Gardini, G; Balbo, A; Bertarelli, D; Girolami, F
1-gen-2006 . Le nuove Frontiere della Nutrizione. Calla', Cinzia Anna Maria
Mostrati risultati da 157 a 176 di 254
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