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

Year Number of Results
1980 1
1981 4
1982 2
1984 2
1985 1
1989 1
1990 2
1991 5
1992 3
1993 4
1994 5
1995 3
1996 1
1997 7
1998 3
1999 6
2000 8
2001 2
2002 7
2003 3
2004 2
2005 2
2006 1
2007 2
2008 2
2009 4
2010 5
2011 4
2012 4
2013 3
2014 4
2015 3
2016 2
2017 2
2018 3
2019 2
2020 3
2021 6
2023 1
2024 0

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119 results

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Page 1
Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Grozeva D, Carss K, Spasic-Boskovic O, Tejada MI, Gecz J, Shaw M, Corbett M, Haan E, Thompson E, Friend K, Hussain Z, Hackett A, Field M, Renieri A, Stevenson R, Schwartz C, Floyd JA, Bentham J, Cosgrove C, Keavney B, Bhattacharya S; Italian X-linked Mental Retardation Project; UK10K Consortium; GOLD Consortium; Hurles M, Raymond FL. Grozeva D, et al. Hum Mutat. 2015 Dec;36(12):1197-204. doi: 10.1002/humu.22901. Epub 2015 Sep 30. Hum Mutat. 2015. PMID: 26350204 Free PMC article.
Molecular Genetics in Neuroblastoma Prognosis.
Lerone M, Ognibene M, Pezzolo A, Martucciello G, Zara F, Morini M, Mazzocco K. Lerone M, et al. Children (Basel). 2021 May 29;8(6):456. doi: 10.3390/children8060456. Children (Basel). 2021. PMID: 34072462 Free PMC article. Review.
Renal involvement and Strømme syndrome.
Caridi G, Lugani F, Lerone M, Divizia MT, Ghiggeri GM, Verrina E. Caridi G, et al. Among authors: lerone m. Clin Kidney J. 2020 Jan 25;14(1):439-441. doi: 10.1093/ckj/sfz189. eCollection 2021 Jan. Clin Kidney J. 2020. PMID: 33564452 Free PMC article.
Pathogenesis of Hirschsprung's disease.
Martucciello G, Ceccherini I, Lerone M, Jasonni V. Martucciello G, et al. Among authors: lerone m. J Pediatr Surg. 2000 Jul;35(7):1017-25. doi: 10.1053/jpsu.2000.7763. J Pediatr Surg. 2000. PMID: 10917288 Review.
Familial Poland anomaly revisited.
Baban A, Torre M, Costanzo S, Gimelli S, Bianca S, Divizia MT, Sénès FM, Garavelli L, Rivieri F, Lerone M, Valle M, Ravazzolo R, Calevo MG. Baban A, et al. Among authors: lerone m. Am J Med Genet A. 2012 Jan;158A(1):140-9. doi: 10.1002/ajmg.a.34370. Epub 2011 Nov 22. Am J Med Genet A. 2012. PMID: 22110015 Review.
Consensus based recommendations for diagnosis and medical management of Poland syndrome (sequence).
Baldelli I, Baccarani A, Barone C, Bedeschi F, Bianca S, Calabrese O, Castori M, Catena N, Corain M, Costanzo S, Barbato GP, De Stefano S, Divizia MT, Feletti F, Formica M, Lando M, Lerone M, Lorenzetti F, Martinoli C, Mellini L, Nava MB, Porcellini G, Puliti A, Romanini MV, Rondoni F, Santi P, Sartini S, Senes F, Spada L, Tarani L, Valle M, Venturino C, Zaottini F, Torre M, Crimi M. Baldelli I, et al. Among authors: lerone m. Orphanet J Rare Dis. 2020 Aug 5;15(1):201. doi: 10.1186/s13023-020-01481-x. Orphanet J Rare Dis. 2020. PMID: 32758259 Free PMC article. Review.
Diagnostic Criteria of Pediatric Intestinal Myopathies.
Lombardi L, Bruder E, Pio L, Nozza P, Thai E, Lerone M, Del Rossi C, Mattioli G, Silini EM, Paraboschi I, Martucciello G. Lombardi L, et al. Among authors: lerone m. J Pediatr Gastroenterol Nutr. 2018 Mar;66(3):383-386. doi: 10.1097/MPG.0000000000001727. J Pediatr Gastroenterol Nutr. 2018. PMID: 28837505
Multiple endocrine neoplasias type 2B and RET proto-oncogene.
Martucciello G, Lerone M, Bricco L, Tonini GP, Lombardi L, Del Rossi CG, Bernasconi S. Martucciello G, et al. Among authors: lerone m. Ital J Pediatr. 2012 Mar 19;38:9. doi: 10.1186/1824-7288-38-9. Ital J Pediatr. 2012. PMID: 22429913 Free PMC article. Review.
Ectodermal dysplasias: not only 'skin' deep.
Priolo M, Silengo M, Lerone M, Ravazzolo R. Priolo M, et al. Among authors: lerone m. Clin Genet. 2000 Dec;58(6):415-30. doi: 10.1034/j.1399-0004.2000.580601.x. Clin Genet. 2000. PMID: 11149610 Review.
119 results