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

Year Number of Results
1974 1
1976 1
1977 1
1978 4
1979 2
1980 1
1981 2
1982 3
1984 2
1986 1
1987 4
1988 2
1990 2
1991 1
1992 5
1993 1
1995 2
1996 1
1997 4
1998 1
1999 9
2000 9
2001 5
2002 5
2003 8
2004 5
2005 4
2006 2
2007 4
2008 7
2009 10
2010 7
2011 9
2012 6
2013 10
2014 7
2015 2
2016 5
2017 3
2018 1
2020 1
2021 3
2024 0

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154 results

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Page 1
SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations.
Lepri F, De Luca A, Stella L, Rossi C, Baldassarre G, Pantaleoni F, Cordeddu V, Williams BJ, Dentici ML, Caputo V, Venanzi S, Bonaguro M, Kavamura I, Faienza MF, Pilotta A, Stanzial F, Faravelli F, Gabrielli O, Marino B, Neri G, Silengo MC, Ferrero GB, Torrrente I, Selicorni A, Mazzanti L, Digilio MC, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M. Lepri F, et al. Among authors: silengo mc. Hum Mutat. 2011 Jul;32(7):760-72. doi: 10.1002/humu.21492. Epub 2011 Apr 28. Hum Mutat. 2011. PMID: 21387466 Free PMC article.
Ectodermal abnormalities in Kabuki syndrome.
Lerone M, Priolo M, Naselli A, Vignolo M, Romeo G, Silengo MC. Lerone M, et al. Among authors: silengo mc. Am J Med Genet. 1997 Dec 19;73(3):263-6. doi: 10.1002/(sici)1096-8628(19971219)73:3<263::aid-ajmg6>3.0.co;2-t. Am J Med Genet. 1997. PMID: 9415681 Review.
Progressive extreme heterotopic calcification.
Silengo M, Defilippi C, Belligni E, Biamino E, Flex E, Brusco A, Ferrero GB, Tartaglia M, Hennekam RC. Silengo M, et al. Am J Med Genet A. 2013 Jul;161A(7):1706-13. doi: 10.1002/ajmg.a.35944. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686761
Fetal growth patterns in Beckwith-Wiedemann syndrome.
Mussa A, Russo S, de Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Silengo MC, Larizza L, Riccio A, Ferrero GB. Mussa A, et al. Among authors: silengo mc. Clin Genet. 2016 Jul;90(1):21-7. doi: 10.1111/cge.12759. Epub 2016 Mar 15. Clin Genet. 2016. PMID: 26857110
Volcanic CO2 tracks the incubation period of basaltic paroxysms.
Aiuppa A, Bitetto M, Delle Donne D, La Monica FP, Tamburello G, Coppola D, Della Schiava M, Innocenti L, Lacanna G, Laiolo M, Massimetti F, Pistolesi M, Silengo MC, Ripepe M. Aiuppa A, et al. Among authors: silengo mc. Sci Adv. 2021 Sep 17;7(38):eabh0191. doi: 10.1126/sciadv.abh0191. Epub 2021 Sep 17. Sci Adv. 2021. PMID: 34533982 Free PMC article.
Ectodermal dysplasias: not only 'skin' deep.
Priolo M, Silengo M, Lerone M, Ravazzolo R. Priolo M, et al. Among authors: silengo m. Clin Genet. 2000 Dec;58(6):415-30. doi: 10.1034/j.1399-0004.2000.580601.x. Clin Genet. 2000. PMID: 11149610 Review.
Clinical significance of rare copy number variations in epilepsy: a case-control survey using microarray-based comparative genomic hybridization.
Striano P, Coppola A, Paravidino R, Malacarne M, Gimelli S, Robbiano A, Traverso M, Pezzella M, Belcastro V, Bianchi A, Elia M, Falace A, Gazzerro E, Ferlazzo E, Freri E, Galasso R, Gobbi G, Molinatto C, Cavani S, Zuffardi O, Striano S, Ferrero GB, Silengo M, Cavaliere ML, Benelli M, Magi A, Piccione M, Dagna Bricarelli F, Coviello DA, Fichera M, Minetti C, Zara F. Striano P, et al. Among authors: silengo m. Arch Neurol. 2012 Mar;69(3):322-30. doi: 10.1001/archneurol.2011.1999. Epub 2011 Nov 14. Arch Neurol. 2012. PMID: 22083797 Free article. Review.
154 results