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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 1 |
2014 | 1 |
2018 | 1 |
2022 | 4 |
2023 | 1 |
2024 | 0 |
Search Results
7 results
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Page 1
A prospective multicentric study of risk-reducing salpingo-oophorectomy in BRCA mutation patients.
Acta Biomed. 2022 Aug 31;93(4):e2022051. doi: 10.23750/abm.v93i4.11695.
Acta Biomed. 2022.
PMID: 36043985
Free PMC article.
Prenatal overgrowth and polydramnios: Would you think about Noonan syndrome?
Beltrami B, Cerasani J, Consales A, Villa R, Resta N, Loconte DC, Boito S, Caschera L, Bassi L, Colombo L, Iascone M, Bedeschi MF.
Beltrami B, et al. Among authors: loconte dc.
Clin Case Rep. 2022 Aug 22;10(8):e6256. doi: 10.1002/ccr3.6256. eCollection 2022 Aug.
Clin Case Rep. 2022.
PMID: 36017115
Free PMC article.
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Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants.
Mussa A, Leoni C, Iacoviello M, Carli D, Ranieri C, Pantaleo A, Buonuomo PS, Bagnulo R, Ferrero GB, Bartuli A, Melis D, Maitz S, Loconte DC, Turchiano A, Piglionica M, De Luisi A, Susca FC, Bukvic N, Forleo C, Selicorni A, Zampino G, Onesimo R, Cappuccio G, Garavelli L, Novelli C, Memo L, Morando C, Della Monica M, Accadia M, Capurso M, Piscopo C, Cereda A, Di Giacomo MC, Saletti V, Spinelli AM, Lastella P, Tenconi R, Dvorakova V, Irvine AD, Resta N.
Mussa A, et al. Among authors: loconte dc.
J Med Genet. 2023 Feb;60(2):163-173. doi: 10.1136/jmedgenet-2021-108093. Epub 2022 Mar 7.
J Med Genet. 2023.
PMID: 35256403
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Beyond BRCA1/2: Homologous Recombination Repair Genetic Profile in a Large Cohort of Apulian Ovarian Cancers.
Turchiano A, Loconte DC, De Nola R, Arezzo F, Chiarello G, Pantaleo A, Iacoviello M, Bagnulo R, De Luisi A, Perrelli S, Martino S, Ranieri C, Garganese A, Stella A, Forleo C, Loizzi V, Marinaccio M, Cicinelli E, Cormio G, Resta N.
Turchiano A, et al. Among authors: loconte dc.
Cancers (Basel). 2022 Jan 12;14(2):365. doi: 10.3390/cancers14020365.
Cancers (Basel). 2022.
PMID: 35053526
Free PMC article.
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Accurate Classification of NF1 Gene Variants in 84 Italian Patients with Neurofibromatosis Type 1.
Stella A, Lastella P, Loconte DC, Bukvic N, Varvara D, Patruno M, Bagnulo R, Lovaglio R, Bartolomeo N, Serio G, Resta N.
Stella A, et al. Among authors: loconte dc.
Genes (Basel). 2018 Apr 17;9(4):216. doi: 10.3390/genes9040216.
Genes (Basel). 2018.
PMID: 29673180
Free PMC article.
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A rare MSH2 mutation causes defective binding to hMSH6, normal hMSH2 staining, and loss of hMSH6 at advanced cancer stage.
Loconte DC, Patruno M, Lastella P, Di Gregorio C, Grossi V, Forte G, Ingravallo G, Varvara D, Bagnulo R, Simone C, Resta N, Stella A.
Loconte DC, et al.
Hum Pathol. 2014 Oct;45(10):2162-7. doi: 10.1016/j.humpath.2014.05.019. Epub 2014 Jun 30.
Hum Pathol. 2014.
PMID: 25106712
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Cancer risk associated with STK11/LKB1 germline mutations in Peutz-Jeghers syndrome patients: results of an Italian multicenter study.
Resta N, Pierannunzio D, Lenato GM, Stella A, Capocaccia R, Bagnulo R, Lastella P, Susca FC, Bozzao C, Loconte DC, Sabbà C, Urso E, Sala P, Fornasarig M, Grammatico P, Piepoli A, Host C, Turchetti D, Viel A, Memo L, Giunti L, Stigliano V, Varesco L, Bertario L, Genuardi M, Lucci Cordisco E, Tibiletti MG, Di Gregorio C, Andriulli A, Ponz de Leon M; AIFEG.
Resta N, et al. Among authors: loconte dc.
Dig Liver Dis. 2013 Jul;45(7):606-11. doi: 10.1016/j.dld.2012.12.018. Epub 2013 Feb 15.
Dig Liver Dis. 2013.
PMID: 23415580
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