Search Results - "Roversi, G"

Identification of novel genomic markers related to progression to glioblastoma through genomic profiling of 25 primary glioma cell lines by ROVERSI, G, PFUNDT, R, MORONI, R. F, MAGNANI, I, VAN REIJMERSDAL, S, POLIO, B, STRAATMAN, H, LARIZZA, L, SCHOENMAKERS, E. F. P. M

“…Identification of genetic copy number changes in glial tumors is of importance in the context of improved/refined diagnostic, prognostic procedures and…”
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Serum levels of anti-apolipoprotein A-1 IGG are associated with long-term disability and cerebral lesion volume in acute ischemic stroke patients by Satta, N, Carbone, F, Montecucco, F, Virzi, J, Burger, F, Roth, A, Roversi, G, Tamborino, C, Casetta, I, Seraceni, S, Trentini, A, Padroni, M, Dallegri, F, Lalive, P, Mach, F, Fainardi, E, Vuilleumier, N

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55. Neurophysiological monitoring during Duodopa therapy for Parkinson’s disease (PD) by Sette, E, Capone, J.G, Sensi, M, Simioni, V, Roversi, G, Tugnoli, V

“…Levodopa/carbidopa intra-duodenal gel (LCIG) was recently introduced as effective therapy in the management of motor complications of PD. In literature…”
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RNA hyperediting and alternative splicing of hematopoietic cell phosphatase (PTPN6) gene in acute myeloid leukemia by BEGHINI, Alessandro, RIPAMONTI, Carla B, PETERLONGO, Paolo, ROVERSI, Gaia, CAIROLI, Roberto, MORRA, Enrica, LARIZZA, Lidia

“…The SH2 domain-containing tyrosine phosphatase PTPN6 (SHP-1, PTP1C, HCP) is a 68 kDa cytoplasmic protein primarily expressed in hematopoietic cell development,…”
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Clericuzio‐type poikiloderma with neutropenia syndrome in three sibs with mutations in the C16orf57 gene: Delineation of the phenotype by Concolino, D., Roversi, G., Muzzi, G.L., Sestito, S., Colombo, E.A., Volpi, L., Larizza, L., Strisciuglio, P.

“…We report on three sibs who have autosomal recessive Clericuzio‐type poikiloderma neutropenia (PN) syndrome. Recently, this consanguineous family was reported…”
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Search for genomic imbalances in a cohort of 24 Cornelia de Lange patients negative for mutations in the NIPBL and SMC1L1 genes by Gervasini, C, Pfundt, R, Castronovo, P, Russo, S, Roversi, G, Masciadri, M, Milani, D, Zampino, G, Selicorni, A, Schoenmakers, EFPM, Larizza, L

“…Cornelia de Lange syndrome (CdLS) is a rare, multiple congenital anomaly/mental retardation syndrome characterized by varied clinical signs including facial…”
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Healthcare resource utilization following apical prolapse surgery in women who received in-office versus phone-only preoperative teaching by Lua-Mailland, L.L., Roversi, G., Yao, M., Ferrando, C.

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Opportunistic Rainfall Sensing: State of the Art and Perspectives in Italy by Giannetti, F., Lottici, V., Sapienza, F., Porcu, F., Roversi, G., Alberoni, P. P., Covi, E., Nebuloni, R., Cazzaniga, G., De Michele, C., Deidda, C., Colli, M., Zani, S., Gianoglio, C., Caviglia, D.D., Adirosi, E.

“…Opportunistic rainfall sensing through the wireless links deployed by telecommunication companies and service providers is an interesting use case of the…”
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Commercial microwave links as a tool for operational rainfall monitoring in Northern Italy by Roversi, Giacomo, Alberoni, Pier Paolo, Fornasiero, Anna, Porcù, Federico

“…There is a growing interest in emerging opportunistic sensors for precipitation, motivated by the need to improve its quantitative estimates at the ground. The…”
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Identification of two novel RECQL4 exonic SNPs and genomic characterization of the IVS12 minisatellite by Roversi, G., Beghini, A., Zambruno, G., Paradisi, M., Larizza, L.

“…Rothmund-Thomson syndrome is a rare autosomal recessive disorder characterized by a widely heterogeneous clinical presentation. Only a subset of clinically…”
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Rothmund–Thomson syndrome and RECQL4 defect: Splitting and lumping by Larizza, Lidia, Magnani, Ivana, Roversi, Gaia

“…Rothmund–Thomson Syndrome (RTS) is a rare autosomal recessive genodermatosis with a heterogeneous clinical profile. Mutations in RECQL4, encoding a RecQ DNA…”
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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers by Kuchenbaecker, Karoline B, Neuhausen, Susan L, Robson, Mark, Barrowdale, Daniel, McGuffog, Lesley, Mulligan, Anna Marie, Andrulis, Irene L, Spurdle, Amanda B, Schmidt, Marjanka K, Schmutzler, Rita K, Engel, Christoph, Wappenschmidt, Barbara, Nevanlinna, Heli, Thomassen, Mads, Southey, Melissa, Radice, Paolo, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Lee, Andrew, Healey, Sue, Nussbaum, Robert L, Rebbeck, Timothy R, Arun, Banu K, James, Paul, Karlan, Beth Y, Lester, Jenny, Cass, Ilana, Terry, Mary Beth, Daly, Mary B, Goldgar, David E, Buys, Saundra S, Janavicius, Ramunas, Tihomirova, Laima, Tung, Nadine, Dorfling, Cecilia M, van Rensburg, Elizabeth J, Steele, Linda, v O Hansen, Thomas, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C, Dennis, Joe, Cunningham, Julie, Hart, Steven, Slager, Susan, Osorio, Ana, Benitez, Javier, Duran, Mercedes, Weitzel, Jeffrey N, Tafur, Isaac, Hander, Mary, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Roversi, Gaia, Scuvera, Giulietta, Bonanni, Bernardo, Mariani, Paolo, Volorio, Sara, Dolcetti, Riccardo, Varesco, Liliana, Papi, Laura, Tibiletti, Maria Grazia, Giannini, Giuseppe, Fostira, Florentia, Konstantopoulou, Irene, Garber, Judy, Hamann, Ute, Donaldson, Alan, Brewer, Carole, Foo, Claire, Evans, D Gareth, Frost, Debra, Eccles, Diana, Douglas, Fiona, Brady, Angela, Cook, Jackie, Tischkowitz, Marc, Adlard, Julian, Barwell, Julian, Ong, Kai-ren, Walker, Lisa, Izatt, Louise, Side, Lucy E, Kennedy, M John, Rogers, Mark T, Porteous, Mary E, Morrison, Patrick J, Platte, Radka, Eeles, Ros, Davidson, Rosemarie, Hodgson, Shirley, Ellis, Steve, Godwin, Andrew K, Rhiem, Kerstin, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg

“…More than 70 common alleles are known to be involved in breast cancer (BC) susceptibility, and several exhibit significant heterogeneity in their associations…”
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Damage to the crystalline lens in infants of diabetic mothers: a pathology so far neglected? by Roversi, G D, Giavini, E

“…Congenital cataract occurs in 90-95% of diabetic rat fetuses. The pathogenetic mechanism is triggered by fetal hyperglycemia and presents the following steps:…”
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Germline mutation in the juxtamembrane domain of the kit gene in a family with gastrointestinal stromal tumors and urticaria pigmentosa by Beghini, Alessandro, Tibiletti, MariaGrazia, Roversi, Gaia, Chiaravalli, AnnaMaria, Serio, Giovanni, Capella, Carlo, Larizza, Lidia

“…BACKGROUND Gain‐of‐function mutations of the c‐kit protooncogene, mainly clustered in the juxtamembrane domain, have been reported in a significant fraction of…”
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Intensive treatment of diabetes during pregnancy by Roversi, G D

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Sonographic determination of fetal weights in diabetic pregnancies by Roversi, G D, Grasso, S

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Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers by RAMUS, Susan J, KARTSONAKI, Christiana, XIANSHU WANG, FREDERICKSEN, Zachary, PETERLONGO, Paolo, MANOUKIAN, Siranoush, PEISSEL, Bernard, ZAFFARONI, Daniela, ROVERSI, Gaia, BARILE, Monica, VIEL, Alessandra, ALLAVENA, Anna, GAYTHER, Simon A, OTTINI, Laura, PAPI, Laura, GISMONDI, Viviana, CAPRA, Fabio, RADICE, Paolo, GREENE, Mark H, MAI, Phuong L, ANDRULIS, Irene L, GLENDON, Gord, OZCELIK, Hilmi, PHAROAH, Paul D. P, THOMASSEN, Mads, GERDES, Anne-Marie, KRUSE, Torben A, CRUGER, Dorthe, JENSEN, Uffe Birk, CALIGO, Maria Adelaide, OLSSON, Hakan, KRISTOFFERSSON, Ulf, LINDBLOM, Annika, ARVER, Brita, SINILNIKOVA, Olga M, KARLSSON, Per, ASKMALM, Marie Stenmark, BORG, Ake, NEUHAUSEN, Susan L, YUAN CHUN DING, NATHANSON, Katherine L, DOMCHEK, Susan M, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BEESLEY, Jonathan, BYRSKI, Tomasz, GRONWALD, Jacek, GORSKI, Bohdan, CYBULSKI, Cezary, DEBNIAK, Tadeusz, OSORIO, Ana, DURAN, Mercedes, TEJADA, Maria-Isabel, BENITEZ, Javier, HAMANN, Ute, XIAOQING CHEN, MCGUFFOG, Lesley, HEALEY, Sue, COUCH, Fergus J

“…Germline mutations in the BRCA1 and BRCA2 genes are associated with increased risks of breast and ovarian cancers. Although several common variants have been…”
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Diet composition modifies embryotoxic effects induced by experimental diabetes in rats by Giavini, E, Broccia, M L, Prati, M, Domenico Roversi, G

“…Despite improvements in prenatal care, the incidence of congenital malformations in diabetic pregnancies is still 3-4 times higher than in normal pregnancies…”
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Effects of diets with different content in protein and fiber on embryotoxicity induced by experimental diabetes in rats by Giavini, E, Airoldi, L, Broccia, M L, Roversi, G D, Prati, M

“…Three groups of streptozotocin-diabetic rats were maintained during pregnancy on three hyperproteic diets with different protein contents. These differences…”
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A new approach to the treatment of diabetic pregnant women. Report of 479 cases seen from 1963 to 1975 by Roversi, G D, Gargiulo, M, Nicolini, U, Pedretti, E, Marini, A, Barbarani, V, Peneff, P

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