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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 1
2005 1
2007 1
2008 1
2009 1
2011 4
2012 2
2014 2
2015 1
2019 2
2020 3
2021 3
2022 2
2023 4
2024 2

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30 results

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Page 1
Pregnancy After Breast Cancer in Young BRCA Carriers: An International Hospital-Based Cohort Study.
Lambertini M, Blondeaux E, Agostinetto E, Hamy AS, Kim HJ, Di Meglio A, Bernstein Molho R, Hilbers F, Pogoda K, Carrasco E, Punie K, Bajpai J, Ignatiadis M, Moore HCF, Phillips KA, Toss A, Rousset-Jablonski C, Peccatori FA, Renaud T, Ferrari A, Paluch-Shimon S, Fruscio R, Cui W, Wong SM, Vernieri C, Ruddy KJ, Dieci MV, Matikas A, Rozenblit M, Villarreal-Garza C, De Marchis L, Del Mastro L, Puglisi F, Del Pilar Estevez-Diz M, Rodriguez-Wallberg KA, Mrinakova B, Meister S, Livraghi L, Clatot F, Yerushalmi R, De Angelis C, Sánchez-Bayona R, Meattini I, Cichowska-Cwalinska N, Berlière M, Salama M, De Giorgi U, Sonnenblick A, Chiodi C, Lee YJ, Maria C, Azim HA Jr, Boni L, Partridge AH; BRCA BCY Collaboration. Lambertini M, et al. JAMA. 2024 Jan 2;331(1):49-59. doi: 10.1001/jama.2023.25463. JAMA. 2024. PMID: 38059899
PRPH2-Associated Retinopathy: Novel Variants and Genotype-Phenotype Correlations.
Bianco L, Arrigo A, Antropoli A, Saladino A, Spiga I, Patricelli MG, Bandello F, Carrera P, Battaglia Parodi M. Bianco L, et al. Among authors: patricelli mg. Ophthalmol Retina. 2023 May;7(5):450-461. doi: 10.1016/j.oret.2022.12.008. Epub 2022 Dec 21. Ophthalmol Retina. 2023. PMID: 36563963
Expanding the spectrum of neonatal-onset AIFM1-associated disorders.
Zambon AA, Ghezzi D, Baldoli C, Cutillo G, Fontana K, Sofia V, Patricelli MG, Nasca A, Vinci S, Spiga I, Lamantea E, Fanelli GF, Sora MGN, Rovelli R, Poloniato A, Carrera P, Filippi M, Barera G. Zambon AA, et al. Among authors: patricelli mg. Ann Clin Transl Neurol. 2023 Oct;10(10):1844-1853. doi: 10.1002/acn3.51876. Epub 2023 Aug 29. Ann Clin Transl Neurol. 2023. PMID: 37644805 Free PMC article.
Oral and Fecal Microbiota in Lynch Syndrome.
Ferrarese R, Zuppardo RA, Puzzono M, Mannucci A, Amato V, Ditonno I, Patricelli MG, Raucci AR, Clementi M, Elmore U, Rosati R, Testoni PA, Mancini N, Cavestro GM. Ferrarese R, et al. Among authors: patricelli mg. J Clin Med. 2020 Aug 24;9(9):2735. doi: 10.3390/jcm9092735. J Clin Med. 2020. PMID: 32847083 Free PMC article.
Age and sex prevalence estimate of Joubert syndrome in Italy.
Nuovo S, Bacigalupo I, Ginevrino M, Battini R, Bertini E, Borgatti R, Casella A, Micalizzi A, Nardella M, Romaniello R, Serpieri V, Zanni G, Valente EM, Vanacore N; JS Italian Study Group. Nuovo S, et al. Neurology. 2020 Feb 25;94(8):e797-e801. doi: 10.1212/WNL.0000000000008996. Epub 2020 Jan 22. Neurology. 2020. PMID: 31969461 Free PMC article.
Newborn Screening for Congenital Hypothyroidism: the Benefit of Using Differential TSH Cutoffs in a 2-Screen Program.
Caiulo S, Corbetta C, Di Frenna M, Medda E, De Angelis S, Rotondi D, Vincenzi G, de Filippis T, Patricelli MG, Persani L, Barera G, Weber G, Olivieri A, Vigone MC. Caiulo S, et al. Among authors: patricelli mg. J Clin Endocrinol Metab. 2021 Jan 1;106(1):e338-e349. doi: 10.1210/clinem/dgaa789. J Clin Endocrinol Metab. 2021. PMID: 33124651 Free article.
Risk factors and clinical characteristics of early-onset colorectal cancer vs. late-onset colorectal cancer: a case-case study.
Di Leo M, Zuppardo RA, Puzzono M, Ditonno I, Mannucci A, Antoci G, Russo Raucci A, Patricelli MG, Elmore U, Tamburini AM, Albarello L, Azzolini F, Bonura GF, Esposito D, Fanti L, Notaristefano C, Viale E, Perea J, Testoni PA, Rosati R, Cavestro GM. Di Leo M, et al. Among authors: patricelli mg. Eur J Gastroenterol Hepatol. 2021 Sep 1;33(9):1153-1160. doi: 10.1097/MEG.0000000000002000. Eur J Gastroenterol Hepatol. 2021. PMID: 33208680
Inverted duplications: how many of them are mosaic?
Pramparo T, Giglio S, Gregato G, de Gregori M, Patricelli MG, Ciccone R, Scappaticci S, Mannino G, Lombardi C, Pirola B, Giorda R, Rocchi M, Zuffardi O. Pramparo T, et al. Among authors: patricelli mg. Eur J Hum Genet. 2004 Sep;12(9):713-7. doi: 10.1038/sj.ejhg.5201240. Eur J Hum Genet. 2004. PMID: 15266302
30 results