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

Year Number of Results
1992 1
1993 1
1994 3
1998 1
2001 1
2002 1
2003 4
2004 2
2005 6
2006 4
2011 2
2020 1
2021 1
2024 0

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26 results

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Page 1
Photoparoxysmal responses in children with chromosomal aberrations.
Grosso S, Pucci L, Bartalini G, Anichini C, Di Bartolo RM, Bazzotti S, Morgese G, Balestri P. Grosso S, et al. Among authors: di bartolo rm. Epilepsy Res. 2006 Dec;72(2-3):164-70. doi: 10.1016/j.eplepsyres.2006.07.016. Epub 2006 Sep 20. Epilepsy Res. 2006. PMID: 16987638
Chromosome 18 aberrations and epilepsy: a review.
Grosso S, Pucci L, Di Bartolo RM, Gobbi G, Bartalini G, Anichini C, Scarinci R, Balestri M, Farnetani MA, Cioni M, Morgese G, Balestri P. Grosso S, et al. Among authors: di bartolo rm. Am J Med Genet A. 2005 Apr 1;134A(1):88-94. doi: 10.1002/ajmg.a.30575. Am J Med Genet A. 2005. PMID: 15690352
Vigabatrin treatment in children.
Fois A, Buoni S, Di Bartolo RM, Di Marco V, Mostardini R. Fois A, et al. Among authors: di bartolo rm. Childs Nerv Syst. 1994 May;10(4):244-8. doi: 10.1007/BF00301162. Childs Nerv Syst. 1994. PMID: 7923235 Clinical Trial.
Atypical BECTS and homocystinuria.
Buoni S, Di Bartolo RM, Molinelli M, Palmeri S, Zannolli R. Buoni S, et al. Among authors: di bartolo rm. Neurology. 2003 Oct 28;61(8):1129-31. doi: 10.1212/01.wnl.0000090460.77321.b0. Neurology. 2003. PMID: 14581679
Electroencephalographic and epileptic patterns in X chromosome anomalies.
Grosso S, Farnetani MA, Di Bartolo RM, Berardi R, Pucci L, Mostardini R, Anichini C, Bartalini G, Galimberti D, Morgese G, Balestri P. Grosso S, et al. Among authors: di bartolo rm. J Clin Neurophysiol. 2004 Jul-Aug;21(4):249-53. doi: 10.1097/00004691-200407000-00003. J Clin Neurophysiol. 2004. PMID: 15509914
Myoclonic encephalopathy in the CDKL5 gene mutation.
Buoni S, Zannolli R, Colamaria V, Macucci F, di Bartolo RM, Corbini L, Orsi A, Zappella M, Hayek J. Buoni S, et al. Among authors: di bartolo rm. Clin Neurophysiol. 2006 Jan;117(1):223-7. doi: 10.1016/j.clinph.2005.09.008. Epub 2005 Dec 2. Clin Neurophysiol. 2006. PMID: 16326141
Childhood absence epilepsy: evolution and prognostic factors.
Grosso S, Galimberti D, Vezzosi P, Farnetani M, Di Bartolo RM, Bazzotti S, Morgese G, Balestri P. Grosso S, et al. Among authors: di bartolo rm. Epilepsia. 2005 Nov;46(11):1796-801. doi: 10.1111/j.1528-1167.2005.00277.x. Epilepsia. 2005. PMID: 16302860 Free article.
Celiac disease and epilepsy in pediatric patients.
Fois A, Vascotto M, Di Bartolo RM, Di Marco V. Fois A, et al. Among authors: di bartolo rm. Childs Nerv Syst. 1994 Sep;10(7):450-4. doi: 10.1007/BF00303610. Childs Nerv Syst. 1994. PMID: 7842435
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family.
Zannolli R, Pierluigi M, Pucci L, Lagrasta N, Gasparre O, Matera MR, Di Bartolo RM, Mazzei MA, Sacco P, Miracco C, de Santi MM, Aitiani P, Cavani S, Pellegrini L, Fimiani M, Alessandrini C, Galluzzi P, Livi W, Gonnelli S, Terrosi-Vagnoli P, Zappella M, Morgese G. Zannolli R, et al. Among authors: di bartolo rm. Am J Med Genet A. 2003 Jan 15;116A(2):192-9. doi: 10.1002/ajmg.a.10069. Am J Med Genet A. 2003. PMID: 12494443
26 results