IRIS

FERRARI, MAURIZIO

FERRARI, MAURIZIO  

Facoltà di Medicina e Chirurgia  

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Risultati 1 - 20 di 195 (tempo di esecuzione: 0.03 secondi).
Titolo Data di pubblicazione Autore(i) File
A Brugada Syndrome mutation (p.S216L) and its modulation by p.H558R polymorphism: standard and dynamic characterization 1-gen-2011 Marangoni, S; DI RESTA, Chiara; Rocchetti, M; Barile, L; Rizzetto, R; Summa, A; Severi, S; Sommariva, E; Pappone, C; Ferrari, Maurizio; Benedetti, S; Zaza, A.
A child with severe pneumomediastinum and ABCA3 gene mutation: a puzzling connection. 1-gen-2012 Copertino, M; Barbi, E; Poli, F; Zennaro, F; Ferrari, Maurizio; Carrera, P; Ventura, A.
A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia 1-gen-2008 Foglieni, B; Galbiati, S; Ferrari, Maurizio; Cremonesi, L.
A new CACNA1A Gene Mutation in Familial Hemiplegic Migraine Acetazolamide-Responsive and Ataxia 1-gen-1999 Battistini, S.; Stenirri, S.; Piatti, M.; Gelfi, C.; Righetti, P. G.; Rocchi, R.; Giannini, F.; Battistini, N.; Guazzi, G. C.; Ferrari, Maurizio; Carrera, P.
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. 1-gen-2015 Scarlato, M; Nuara, A; Gerevini, S; Benedetti, S; P., Rossi; Ferrari, Maurizio; Previtali, S. C.
A new microarray substrate for ultra-sensitive genotyping of KRAS and BRAF gene variants in colorectal cancer. 1-gen-2013 Galbiati, S; Damin, F; Pinzani, P; Mancini, I; Vinci, S; Chiari, M; Orlando, C; Cremonesi, L; Ferrari, Maurizio
A novel homozygous mutation in the TRDN gene causes a severe form of pediatric malignant ventricular arrhythmia 1-gen-2020 Rossi, D.; Gigli, L.; Gamberucci, A.; Bordoni, R.; Pietrelli, A.; Lorenzini, S.; Pierantozzi, E.; Peretto, G.; De Bellis, G.; Della Bella, P.; Ferrari, M.; Sorrentino, V.; Benedetti, S.; Sala, S.; Di Resta, C.
A novel LIPS assay for insulin autoantibodies 1-gen-2018 Liberati, Daniela; Wyatt, Rebecca C.; Brigatti, Cristina; Marzinotto, Ilaria; Ferrari, Maurizio; Bazzigaluppi, Elena; Bosi, Emanuele; Gillard, Ben T.; Gillespie, Kathleen M.; Gorus, Frans; Weets, Ilse; Balti, Eric; Piemonti, Lorenzo; Achenbach, Peter; Williams, Alistair J. K.; Lampasona, Vito
A novel MEN1 gene mutation 1-gen-2008 Manzoni, Mf; Franchi, Gm; Sartorio, Sm; Di Rosa, E; Cappelletti, C; Piani, C; Cattaneo, C; Ferrari, Maurizio; Bosi, Emanuele; Carrera, P.
A whole-genome sequencing study associates GRAMD1B with multiple sclerosis risk and disease activity 1-gen-2017 Osiceanu, Am; Esposito, F; Bollman, B; Sorosina, M; Santoro, S; Bettegazzi, B; Zauli, A; Clarelli, F; Ottoboni, L; Mascia, E; Zacchetti, D; Capra, R; Ferrari, M; Provero, P; Lazarevic, D; Stupka, E; Carrera, P; Patsopoulos, N; Toniolo, D; Martino, G; Tonon, G; Comi, G; De Jager, P; Piccio, L; Boneschi, Fm
A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility 1-gen-2022 Esposito, F.; Osiceanu, A. M.; Sorosina, M.; Ottoboni, L.; Bollman, B.; Santoro, S.; Bettegazzi, B.; Zauli, A.; Clarelli, F.; Mascia, E.; Calabria, A.; Zacchetti, D.; Capra, R.; Ferrari, M.; Provero, P.; Lazarevic, D.; Cittaro, D.; Carrera, P.; Patsopoulos, N.; Toniolo, D.; Sadovnick, A. D.; Martino, G.; De Jager, P. L.; Comi, G.; Stupka, E.; Vilarino-Guell, C.; Piccio, L.; Martinelli Boneschi, F.
Advancing the education in molecular diagnostics: The IFCC-Initiative "Clinical Molecular Biology Curriculum" (C-CMBC); A ten-year experience 1-gen-2014 Lianidou, E; Ahmad Nejad, P; Ferreira Gonzalez, A; Izuhara, K; Cremonesi, L; Schroeder, Me; Richter, K; Ferrari, Maurizio; Neumaier, M.
An approach for screening of Hereditary Hyperferritinemia Cataract Syndrome (HHCS) by a new DG-DGGE method for rapid mutational scanning in ferritin L-chain IRE. 1-gen-1999 Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Tinazzi, E; Camparini, M; Aldigeri, R; Girelli, D; Arosio, P; Levi, SONIA MARIA ROSA
An overview of current microarray-based human globin gene mutation detection methods 1-gen-2007 Cremonesi, L; Ferrari, M; Giordano, Pc; Harteveld, Cl; Kleanthous, M; Papasavva, T; Patrinos, Gp; TRAEGER-SYNODINOS, J
Analysis of clinically relevant single nucleotide polymorphisms by use of microelectronic array technology 1-gen-2002 Santacroce, R; Ratti, A; Caroli, F; Foglieni, B; Cremonesi, L; Ferraris, A; Margaglione, M; Seri, M; Ravazzolo, R; Dallapiccola, B; Rappaport, E; Pollack, E; Surrey, S; Mcentire, Je; Ferrari, Maurizio; Fortina, P.
Analysis of ferritin genes in Parkinson disease. 1-gen-2007 Foglieni, B; Ferrari, F; Goldwurm, S; Santambrogio, P; Castiglioni, E; Sessa, M; Volontè, Ma; Lalli, S; Galli, C; Wang, Xs; Connor, J; Sironi, F; Canesi, M; Biasiotto, G; Pezzoli, G; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Cremonesi, L.
Analysis of KRAS, NRAS and BRAF mutational profile by combination of in-tube hybridization and universal tag-microarray in tumor tissue and plasma of colorectal cancer patients 1-gen-2018 Damin, Francesco; Galbiati, Silvia; Soriani, Nadia; Burgio, Valentina; Ronzoni, Monica; Ferrari, Maurizio; Chiari, Marcella
Analysis of nucleotide variations in genes of iron management in patients of Parkinson’s disease and other movement disorders. 1-gen-2011 Castiglioni, E; Finazzi, D; Goldwurm, S; Pezzoli, G; Nardocci, N; Forni, G; Girelli, D; Maccarinelli, F; Poli, M; Ferrari, Maurizio; Cremonesi, L; Arosio, P.
Analytical Ancestry: Evolution of the Array in Analysis 1-gen-2012 Ferrari, Maurizio; DI RESTA, Chiara
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis 1-gen-2010 Benedetti, S; Previtali, Sc; Coviello, S; Scarlato, M; Cerri, F; DI PIERRI, E; Piantoni, L; Spiga, I; Fazio, R; Riva, N; NATALI SORA, Mg; Dacci, P; Malaguti, Mc; Munerati, E; Grimaldi, Lm; Marrosu, Mg; DE PELLEGRIN, M; Ferrari, Maurizio; Comi, Giancarlo; Quattrini, A; Bolino, A.