Prognostic Impact of Node-Spreading Pattern in Surgically Treated Small-Cell Lung Cancer: A Multicentric Analysis
Leuzzi, Giovanni, Lococo, Filippo, Alessandrini, Gabriele, Sperduti, Isabella, Spaggiari, Lorenzo, Venuta, Federico, Rendina, Erino A., Granone, Pierluigi M., Rapicetta, Cristian, Zannini, Piero, Di Rienzo, Gaetano, Nicolosi, Maurizio, Facciolo, Francesco
Published in Lung (01.02.2017)
Published in Lung (01.02.2017)
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First-trimester euploid miscarriages analysed by array-CGH
Viaggi, Chiara Donatella, Cavani, S, Malacarne, M, Floriddia, F, Zerega, G, Baldo, C, Mogni, M, Castagnetta, M, Piombo, G, Coviello, D. A, Camandona, F, Lijoi, D, Insegno, W, Traversa, M, Pierluigi, M
Published in Journal of applied genetics (01.08.2013)
Published in Journal of applied genetics (01.08.2013)
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Cryptic chromosome deletions involving SCN1A in severe myoclonic epilepsy of infancy
Madia, F, Striano, P, Gennaro, E, Malacarne, M, Paravidino, R, Biancheri, R, Budetta, M, Cilio, M R, Gaggero, R, Pierluigi, M, Minetti, C, Zara, F
Published in Neurology (10.10.2006)
Published in Neurology (10.10.2006)
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Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation
Mainardi, P Cerruti, Perfumo, C, Calì, A, Coucourde, G, Pastore, G, Cavani, S, Zara, F, Overhauser, J, Pierluigi, M, Bricarelli, F Dagna
Published in Journal of medical genetics (01.03.2001)
Published in Journal of medical genetics (01.03.2001)
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Array‐CGH and clinical characterization in a patient with subtelomeric 6p deletion without ocular dysgenesis
Piccione, Maria, Antona, R., Salzano, E., Cavani, S., Malacarne, M., Morreale Bubella, R., Pierluigi, M., Viaggi, C.D., Corsello, Giovanni
Published in American journal of medical genetics. Part A (01.01.2012)
Published in American journal of medical genetics. Part A (01.01.2012)
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Cryptic telomeric rearrangements in subjects with mental retardation associated with dysmorphism and congenital malformations
Rossi, Elena, Piccini, Flavia, Zollino, Marcella, Neri, Giovanni, Caselli, Desirée, Tenconi, Romano, Castellan, Claudio, Carrozzo, Romeo, Danesino, Cesare, Zuffardi, Orsetta, Ragusa, Angela, Castiglia, Lucia, Galesi, Ornella, Greco, Donatella, Romano, Corrado, Pierluigi, Mauro, Perfumo, Chiara, Di Rocco, Maia, Faravelli, Francesca, Bricarelli, Franca Dagna, Bonaglia, MariaClara, Bedeschi, MariaFrancesca, Borgatti, Renato
Published in Journal of medical genetics (01.06.2001)
Published in Journal of medical genetics (01.06.2001)
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Mutation analysis of the NSD1 gene in a group of 59 patients with congenital overgrowth
Cecconi, M., Forzano, F., Milani, D., Cavani, S., Baldo, C., Selicorni, A., Pantaleoni, C., Silengo, M., Ferrero, G.B., Scarano, G., Della Monica, M., Fischetto, R., Grammatico, P., Majore, S., Zampino, G., Memo, L., Cordisco, E. Lucci, Neri, G., Pierluigi, M., Bricarelli, F. Dagna, Grasso, M., Faravelli, Francesca
Published in American journal of medical genetics. Part A (30.04.2005)
Published in American journal of medical genetics. Part A (30.04.2005)
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The first three mosaic cri du chat syndrome patients with two rearranged cell lines
PERFUMO, C, MAINARDI, P CERRUTI, CALÌ, A, COUCOURDE, G, ZARA, F, CAVANI, S, OVERHAUSER, J, BRICARELLI, F DAGNA, PIERLUIGI, M
Published in Journal of medical genetics (01.12.2000)
Published in Journal of medical genetics (01.12.2000)
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The Italian External Quality Assessment Scheme in Classical Cytogenetics: Four Years of Activity
Floridia, G., Falbo, V., Censi, F., Tosto, F., Salvatore, M., Baroncini, A., Battaglia, P., Conti, A., Donti, E., La Starza, R., Nitsch, L., Pierluigi, M., Piombo, G., Susca, F., Mancini, M., Mecucci, C., Calzolari, E., Bricarelli, F. Dagna, Guanti, G., Taruscio, D.
Published in Community genetics (01.01.2008)
Published in Community genetics (01.01.2008)
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Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations
Cavani, S., Perfumo, C., Faravelli, F., Malacarne, M., Sogliani, M., Piombo, G., Zerega, G., Zucca, M., Dagna Bricarelli, F., Pierluigi, M.
Published in Prenatal diagnosis (01.10.2003)
Published in Prenatal diagnosis (01.10.2003)
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Psychomotor development in Cri du Chat Syndrome
Cerruti Mainardi, Paola, Guala, Andrea, Pastore, Guido, Pozzo, Gloria, Dagna Bricarelli, Franca, Pierluigi, Mauro
Published in Clinical genetics (01.06.2000)
Published in Clinical genetics (01.06.2000)
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18q‐ syndrome and ectodermal dysplasia syndrome: Description of a child and his family
Zannolli, R., Pierluigi, M., Pucci, L., Lagrasta, N., Gasparre, O., Matera, M.R., Di Bartolo, R.M., Mazzei, M.A., Sacco, P., Miracco, C., de Santi, M.M., Aitiani, P., Cavani, S., Pellegrini, L., Fimiani, M., Alessandrini, C., Galluzzi, P., Livi, W., Gonnelli, S., Terrosi‐Vagnoli, P., Zappella, M., Morgese, G.
Published in American journal of medical genetics. Part A (15.01.2003)
Published in American journal of medical genetics. Part A (15.01.2003)
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Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings
Mattina, T, Pierluigi, M, Mazzone, D, Scardilli, S, Perfumo, C, Mollica, F
Published in Journal of medical genetics (01.11.1997)
Published in Journal of medical genetics (01.11.1997)
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Novel CNS syndrome and ectodermal dysplasia
Zannolli, R., Macucci, F., Di Bartolo, R.M., Serracca, L., Miracco, C., de Santi, M.M., Giannini, F., Malandrini, A., Galluzzi, P., De Robertis, S., Hadjistilianou, T., Perotti, R., Fimiani, M., Doldo, T., Giorgetti, R., Cavani, S., Pierluigi, M.
Published in American journal of medical genetics. Part A (15.01.2003)
Published in American journal of medical genetics. Part A (15.01.2003)
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Antley-Bixler syndrome
Mattina, T, Pierluigi, M, Perfumo, C, Mazzone, D, Scardilli, S, Mollica, F
Published in Clinical genetics (01.10.1996)
Published in Clinical genetics (01.10.1996)
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An improved method for the detection of Down's syndrome aneuploidy in uncultured amniocytes
Pierluigi, M, Perfumo, C, Cavani, S, Lehrach, H, Nizetic, D, Dagna Bricarelli, F D
Published in Clinical genetics (01.01.1996)
Published in Clinical genetics (01.01.1996)
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Isochromosome not translocation in trisomy 21q21q
Grasso, M, Giovannucci Uzielli, M L, Pierluigi, M, Tavellini, F, Perroni, L, Dagna Bricarelli, F
Published in Human genetics (01.12.1989)
Published in Human genetics (01.12.1989)
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Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25
Ventura, Mario, Mudge, Jonathan M, Palumbo, Valeria, Burn, Sally, Blennow, Elisabeth, Pierluigi, Mauro, Giorda, Roberto, Zuffardi, Orsetta, Archidiacono, Nicoletta, Jackson, Michael S, Rocchi, Mariano
Published in Genome research (01.09.2003)
Published in Genome research (01.09.2003)
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Effect of alirocumab, a monoclonal antibody to PCSK9, on long-term cardiovascular outcomes following acute coronary syndromes: Rationale and design of the ODYSSEY Outcomes trial
Schwartz, Gregory G., MD, PhD, Bessac, Laurence, MD, Berdan, Lisa G., PA, MHS, Bhatt, Deepak L., MD, MPH, Bittner, Vera, MD, Diaz, Rafael, MD, Goodman, Shaun G., MD, MSc, Hanotin, Corinne, MD, Harrington, Robert A., MD, Jukema, J. Wouter, MD, PhD, Mahaffey, Kenneth W., MD, Moryusef, Angèle, MD, Pordy, Robert, MD, Roe, Matthew T., MD, MPH, Rorick, Tyrus, RN, Sasiela, William J., PhD, Shirodaria, Cheerag, MBBS, Szarek, Michael, PhD, Tamby, Jean-François, MD, Tricoci, Pierluigi, MD, White, Harvey, MBBS, DSc, Zeiher, Andreas, MD, Steg, Philippe Gabriel, MD
Published in The American heart journal (01.11.2014)
Published in The American heart journal (01.11.2014)
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