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

Year Number of Results
2002 3
2004 3
2005 3
2006 1
2007 4
2008 5
2009 1
2010 3
2011 2
2012 2
2013 4
2014 3
2015 3
2016 5
2017 4
2018 2
2020 2
2024 0

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46 results

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Page 1
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.
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.
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.
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
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
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients.
Garavelli L, Ivanovski I, Caraffi SG, Santodirocco D, Pollazzon M, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Baldo C, Bayat A, Belligni E, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, Devriendt K, Dinulos MB, Djuric O, Epifanio R, Faravelli F, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Lacombe D, Maggi M, Malbora B, Mammi I, Moutton S, Møller R, Muschke P, Napoli M, Pantaleoni C, Pascarella R, Pellicciari A, Poch-Olive ML, Raviglione F, Rivieri F, Russo C, Savasta S, Scarano G, Selicorni A, Silengo M, Sorge G, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zollino M, Dobyns WB, Paciorkowski AR. Garavelli L, et al. Among authors: sorge g. Genet Med. 2017 Jun;19(6):691-700. doi: 10.1038/gim.2016.176. Epub 2016 Nov 10. Genet Med. 2017. PMID: 27831545 Free PMC article.
Imaging findings of mucopolysaccharidoses: a pictorial review.
Palmucci S, Attinà G, Lanza ML, Belfiore G, Cappello G, Foti PV, Milone P, Di Bella D, Barone R, Fiumara A, Sorge G, Ettorre GC. Palmucci S, et al. Among authors: sorge g. Insights Imaging. 2013 Aug;4(4):443-59. doi: 10.1007/s13244-013-0246-8. Epub 2013 May 5. Insights Imaging. 2013. PMID: 23645566 Free PMC article.
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care.
Ivanovski I, Djuric O, Caraffi SG, Santodirocco D, Pollazzon M, Rosato S, Cordelli DM, Abdalla E, Accorsi P, Adam MP, Ajmone PF, Badura-Stronka M, Baldo C, Baldi M, Bayat A, Bigoni S, Bonvicini F, Breckpot J, Callewaert B, Cocchi G, Cuturilo G, De Brasi D, Devriendt K, Dinulos MB, Hjortshøj TD, Epifanio R, Faravelli F, Fiumara A, Formisano D, Giordano L, Grasso M, Grønborg S, Iodice A, Iughetti L, Kuburovic V, Kutkowska-Kazmierczak A, Lacombe D, Lo Rizzo C, Luchetti A, Malbora B, Mammi I, Mari F, Montorsi G, Moutton S, Møller RS, Muschke P, Nielsen JEK, Obersztyn E, Pantaleoni C, Pellicciari A, Pisanti MA, Prpic I, Poch-Olive ML, Raviglione F, Renieri A, Ricci E, Rivieri F, Santen GW, Savasta S, Scarano G, Schanze I, Selicorni A, Silengo M, Smigiel R, Spaccini L, Sorge G, Szczaluba K, Tarani L, Tone LG, Toutain A, Trimouille A, Valera ET, Vergano SS, Zanotta N, Zenker M, Conidi A, Zollino M, Rauch A, Zweier C, Garavelli L. Ivanovski I, et al. Among authors: sorge g. Genet Med. 2018 Sep;20(9):965-975. doi: 10.1038/gim.2017.221. Epub 2018 Jan 4. Genet Med. 2018. PMID: 29300384 Free article.
46 results