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

Year Number of Results
1977 2
1978 2
1979 2
1980 1
1981 3
1982 2
1983 1
1985 1
1987 1
1989 3
1990 2
1991 1
1993 3
1995 4
1996 5
1997 6
1998 4
2000 5
2001 1
2002 4
2003 1
2004 4
2005 4
2006 2
2007 4
2008 5
2009 3
2010 6
2011 5
2012 4
2013 6
2014 4
2015 5
2016 7
2017 6
2018 2
2020 3
2025 0

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115 results

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Page 1
Spondyloperipheral dysplasia.
Sorge G, Ruggieri M, Lachman RS. Sorge G, et al. Am J Med Genet. 1995 Nov 6;59(2):139-42. doi: 10.1002/ajmg.1320590204. Am J Med Genet. 1995. PMID: 8588574
Trisomy 22 mosaicism.
Mollica F, Sorge G, Pavone L. Mollica F, et al. Among authors: sorge g. J Med Genet. 1977 Jun;14(3):224-5. doi: 10.1136/jmg.14.3.224. J Med Genet. 1977. PMID: 881717 Free PMC article.
Epilepsy and chromosomal abnormalities.
Sorge G, Sorge A. Sorge G, et al. Ital J Pediatr. 2010 May 3;36:36. doi: 10.1186/1824-7288-36-36. Ital J Pediatr. 2010. PMID: 20438626 Free PMC article. Review.
The multiple faces of artwork diagnoses.
Ruggieri M, Praticò AD, Scuderi A, Sorge G, Polizzi A. Ruggieri M, et al. Among authors: sorge g. Lancet Neurol. 2017 Jun;16(6):417-418. doi: 10.1016/S1474-4422(17)30129-1. Lancet Neurol. 2017. PMID: 28504104 No abstract available.
Epilepsy in patients with Angelman syndrome.
Fiumara A, Pittalà A, Cocuzza M, Sorge G. Fiumara A, et al. Among authors: sorge g. Ital J Pediatr. 2010 Apr 16;36:31. doi: 10.1186/1824-7288-36-31. Ital J Pediatr. 2010. PMID: 20398390 Free PMC article. Review.
Aggressive behavior in patients with Sotos syndrome.
Mauceri L, Sorge G, Baieli S, Rizzo R, Pavone L, Coleman M. Mauceri L, et al. Among authors: sorge g. Pediatr Neurol. 2000 Jan;22(1):64-7. doi: 10.1016/s0887-8994(99)00105-8. Pediatr Neurol. 2000. PMID: 10669209 Review.
Mucopolysaccharidosis VI: the Italian experience.
Scarpa M, Barone R, Fiumara A, Astarita L, Parenti G, Rampazzo A, Sala S, Sorge G, Parini R. Scarpa M, et al. Among authors: sorge g. Eur J Pediatr. 2009 Oct;168(10):1203-6. doi: 10.1007/s00431-008-0910-z. Epub 2009 Jan 7. Eur J Pediatr. 2009. PMID: 19130082
[The FF complex: a rare congenital malformation].
Smilari P, Pavone V, Saporito A, Parisi M, Carpinato C, Sorge G. Smilari P, et al. Among authors: sorge g. Pediatr Med Chir. 1997 May-Jun;19(3):215-7. Pediatr Med Chir. 1997. PMID: 9340614 Review. Italian. No abstract available.
Epilepsy in fragile X syndrome.
Incorpora G, Sorge G, Sorge A, Pavone L. Incorpora G, et al. Among authors: sorge g. Brain Dev. 2002 Dec;24(8):766-9. doi: 10.1016/s0387-7604(02)00102-x. Brain Dev. 2002. PMID: 12453600
115 results