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

Year Number of Results
1948 2
1949 2
1950 3
1951 7
1952 5
1953 5
1954 5
1955 2
1956 4
1957 3
1958 2
1959 9
1960 2
1961 2
1962 1
1967 1
1969 2
1970 1
1975 3
1976 2
1978 1
1979 4
1980 2
1981 3
1982 1
1983 1
1984 1
1985 4
1986 3
1987 2
1988 7
1989 3
1990 3
1991 3
1992 1
1993 1
1994 3
1995 3
1996 5
1997 5
1998 5
1999 5
2000 1
2001 7
2002 9
2003 5
2004 1
2005 5
2006 4
2007 4
2008 8
2009 7
2010 4
2011 6
2012 4
2013 5
2014 3
2015 4
2016 4
2017 7
2018 7
2019 7
2020 13
2021 10
2022 16
2023 15
2024 12
2025 5

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280 results

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Page 1
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility.
Leone MP, Morlino S, Nardella G, Pracella R, Giachino D, Celli L, Baldo D, Turolla L, Piccione M, Salzano E, Busè M, Lastella P, Zollino M, Cantone R, Grosso E, Zonta A, Pasini B, Piscopo C, De Maggio I, Priolo M, Mammi C, Foiadelli T, Trabatti C, Savasta S, Iolascon A, Ferraris A, Lodato V, Di Giosaffatte N, Majore S, Selicorni A, Petracca A, Fusco C, Celli M, Guarnieri V, Micale L, Castori M. Leone MP, et al. Among authors: ferraris a. Hum Genet. 2023 Jun;142(6):785-808. doi: 10.1007/s00439-023-02547-z. Epub 2023 Apr 20. Hum Genet. 2023. PMID: 37079061
Neuropsychological tests at the Italian Centers for Cognitive Disorders and Dementias: results from a survey on 450 specialized services.
Vaccaro R, Lorenzini P, Giaquinto F, Matascioli F, Carnevale G, Sciancalepore F, Gasparini M, Salvi E, Corbo M, Locuratolo N, Vanacore N, Bacigalupo I; Permanent Table of the National Dementia Plan Study Group; CCDDs Study Group. Vaccaro R, et al. Aging Clin Exp Res. 2024 Dec 20;37(1):1. doi: 10.1007/s40520-024-02869-6. Aging Clin Exp Res. 2024. PMID: 39704981 Free PMC article.
A new national survey of centers for cognitive disorders and dementias in Italy.
Bacigalupo I, Giaquinto F, Salvi E, Carnevale G, Vaccaro R, Matascioli F, Remoli G, Vanacore N, Lorenzini P; Permanent Table of the National Dementia Plan Study Group and the CCDDs Study Group. Bacigalupo I, et al. Neurol Sci. 2024 Feb;45(2):525-538. doi: 10.1007/s10072-023-06958-8. Epub 2023 Aug 18. Neurol Sci. 2024. PMID: 37592124 Free PMC article.
Sensing Technologies for Extravasation Detection: A Review.
Hirata I, Mazzotta A, Makvandi P, Cesini I, Brioschi C, Ferraris A, Mattoli V. Hirata I, et al. Among authors: ferraris a. ACS Sens. 2023 Mar 24;8(3):1017-1032. doi: 10.1021/acssensors.2c02602. Epub 2023 Mar 13. ACS Sens. 2023. PMID: 36912628 Free PMC article. Review.
Left ventricular dysfunction in COVID-19: A diagnostic issue.
Jacquet-Lagrèze M, Riad Z, Hugon-Vallet E, Ferraris A, Fellahi JL. Jacquet-Lagrèze M, et al. Among authors: ferraris a. Anaesth Crit Care Pain Med. 2020 Jun;39(3):393-394. doi: 10.1016/j.accpm.2020.05.015. Epub 2020 Jun 17. Anaesth Crit Care Pain Med. 2020. PMID: 32562808 Free PMC article. Review. No abstract available.
A Multimodal Cardioprotection Strategy During Cardiac Surgery: The ProCCard Study.
Chiari P, Desebbe O, Durand M, Fischer MO, Lena-Quintard D, Palao JC, Samson G, Varillon Y, Vaz B, Joseph P, Ferraris A, Jacquet-Lagreze M, Pozzi M, Maucort-Boulch D, Ovize M, Bidaux G, Mewton N, Fellahi JL; ProCCard Trial Investigators. Chiari P, et al. Among authors: ferraris a. J Cardiothorac Vasc Anesth. 2023 Aug;37(8):1368-1376. doi: 10.1053/j.jvca.2023.04.011. Epub 2023 Apr 14. J Cardiothorac Vasc Anesth. 2023. PMID: 37202231 Clinical Trial.
Two unrelated cases with biallelic CHEK2 variants:a novel condition with constitutional chromosomal instability?
Bottillo I, Savino E, Majore S, Mulargia C, Valiante M, Ferraris A, Rossi V, Svegliati F, Ciccone MP, Brusco F, Grammatico B, Di Giacomo G, Bargiacchi S, D'Angelantonio D, Grammatico P. Bottillo I, et al. Among authors: ferraris a. Eur J Hum Genet. 2023 Apr;31(4):474-478. doi: 10.1038/s41431-022-01270-z. Epub 2022 Dec 19. Eur J Hum Genet. 2023. PMID: 36529819 Free PMC article.
Biallelic mutations in DYNC2LI1 are a rare cause of Ellis-van Creveld syndrome.
Niceta M, Margiotti K, Digilio MC, Guida V, Bruselles A, Pizzi S, Ferraris A, Memo L, Laforgia N, Dentici ML, Consoli F, Torrente I, Ruiz-Perez VL, Dallapiccola B, Marino B, De Luca A, Tartaglia M. Niceta M, et al. Among authors: ferraris a. Clin Genet. 2018 Mar;93(3):632-639. doi: 10.1111/cge.13128. Epub 2018 Jan 24. Clin Genet. 2018. PMID: 28857138
280 results