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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 6
2011 9
2012 6
2013 7
2014 6
2015 2
2016 3
2017 2
2018 1
2021 3
2022 0
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Search Results

146 results
Results by year
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Page 1
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.
Sarkozy A, Carta C, Moretti S, Zampino G, Digilio MC, Pantaleoni F, Scioletti AP, Esposito G, Cordeddu V, Lepri F, Petrangeli V, Dentici ML, Mancini GM, Selicorni A, Rossi C, Mazzanti L, Marino B, Ferrero GB, Silengo MC, Memo L, Stanzial F, Faravelli F, Stuppia L, Puxeddu E, Gelb BD, Dallapiccola B, Tartaglia M. Sarkozy A, et al. Among authors: silengo mc. Hum Mutat. 2009 Apr;30(4):695-702. doi: 10.1002/humu.20955. Hum Mutat. 2009. PMID: 19206169 Free PMC article.
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 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.
Ground deformation reveals the scale-invariant conduit dynamics driving explosive basaltic eruptions.
Ripepe M, Lacanna G, Pistolesi M, Silengo MC, Aiuppa A, Laiolo M, Massimetti F, Innocenti L, Della Schiava M, Bitetto M, La Monica FP, Nishimura T, Rosi M, Mangione D, Ricciardi A, Genco R, Coppola D, Marchetti E, Delle Donne D. Ripepe M, et al. Among authors: silengo mc. Nat Commun. 2021 Mar 16;12(1):1683. doi: 10.1038/s41467-021-21722-2. Nat Commun. 2021. PMID: 33727536 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.
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
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.
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
146 results