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

Year Number of Results
1990 1
1992 2
1996 1
1997 3
1998 3
1999 3
2000 3
2001 9
2002 3
2003 6
2004 2
2005 4
2007 5
2008 5
2009 3
2010 6
2011 7
2012 2
2013 4
2014 4
2015 5
2016 2
2017 4
2018 8
2019 4
2020 8
2021 9
2022 6
2023 2
2024 0

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108 results

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Page 1
A2 Milk and BCM-7 Peptide as Emerging Parameters of Milk Quality.
Giribaldi M, Lamberti C, Cirrincione S, Giuffrida MG, Cavallarin L. Giribaldi M, et al. Among authors: giuffrida mg. Front Nutr. 2022 Apr 27;9:842375. doi: 10.3389/fnut.2022.842375. eCollection 2022. Front Nutr. 2022. PMID: 35571904 Free PMC article. Review.
2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review.
Bouassida M, Egloff M, Levy J, Chatron N, Bernardini L, Le Guyader G, Tabet AC, Schluth-Bolard C, Brancati F, Giuffrida MG, Dard R, Clorennec J, Coursimault J, Vialard F, Hervé B. Bouassida M, et al. Among authors: giuffrida mg. Eur J Hum Genet. 2023 Aug;31(8):895-904. doi: 10.1038/s41431-023-01379-9. Epub 2023 May 15. Eur J Hum Genet. 2023. PMID: 37188826 Review.
Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes.
Ambrosetti I, Bernardini L, Pollazzon M, Giuffrida MG, Guida V, Peluso F, Baroni MC, Polizzi V, Napoli M, Rosato S, Trimarchi G, Gelmini C, Caraffi SG, Wischmeijer A, Frattini D, Novelli A, Garavelli L. Ambrosetti I, et al. Among authors: giuffrida mg. Genes (Basel). 2023 Jul 26;14(8):1526. doi: 10.3390/genes14081526. Genes (Basel). 2023. PMID: 37628577 Free PMC article. Review.
Chromosomal Microarray Analysis in Fetuses Detected with Isolated Cardiovascular Malformation: A Multicenter Study, Systematic Review of the Literature and Meta-Analysis.
Mastromoro G, Khaleghi Hashemian N, Guadagnolo D, Giuffrida MG, Torres B, Bernardini L, Ventriglia F, Piacentini G, Pizzuti A. Mastromoro G, et al. Among authors: giuffrida mg. Diagnostics (Basel). 2022 May 27;12(6):1328. doi: 10.3390/diagnostics12061328. Diagnostics (Basel). 2022. PMID: 35741137 Free PMC article. Review.
Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.
Hardcastle A, Berry AM, Campbell IM, Zhao X, Liu P, Gerard AE, Rosenfeld JA, Sisoudiya SD, Hernandez-Garcia A, Loddo S, Di Tommaso S, Novelli A, Dentici ML, Capolino R, Digilio MC, Graziani L, Rustad CF, Neas K, Ferrero GB, Brusco A, Di Gregorio E, Wellesley D, Beneteau C, Joubert M, Van Den Bogaert K, Boogaerts A, McMullan DJ, Dean J, Giuffrida MG, Bernardini L, Varghese V, Shannon NL, Harrison RE, Lam WWK, McKee S, Turnpenny PD, Cole T, Morton J, Eason J, Jones MC, Hall R, Wright M, Horridge K, Shaw CA, Chung WK, Scott DA. Hardcastle A, et al. Among authors: giuffrida mg. Am J Med Genet A. 2022 Oct;188(10):2958-2968. doi: 10.1002/ajmg.a.62919. Epub 2022 Jul 29. Am J Med Genet A. 2022. PMID: 35904974 Free PMC article.
108 results