Curatolo P - Search Results

1

Association of Trp53 polymorphic variants at codon 72 with nonsyndromic mental retardation.

Saccucci P, Galasso C, Rizzo R, Gagliano A, Refice F, Lalli C, Verrotti A, Gloria-Bottini F, Curatolo P. Saccucci P, et al. Among authors: curatolo p. Neurosci Res. 2007 Sep;59(1):47-50. doi: 10.1016/j.neures.2007.05.009. Epub 2007 May 31. Neurosci Res. 2007. PMID: 17597242

2

Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphism.

Saccucci P, Verdecchia M, Piciullo A, Bottini N, Rizzo R, Gloria-Bottini F, Lucarelli P, Curatolo P. Saccucci P, et al. Among authors: curatolo p. Neurogenetics. 2004 Dec;5(4):245-8. doi: 10.1007/s10048-004-0192-1. Epub 2004 Oct 14. Neurogenetics. 2004. PMID: 15490286

3

Genetic polymorphism and idiopathic generalized epilepsy. Evidence of interaction between haptoglobin and ACP1 systems.

Gloria-Bottini F, Lucarelli P, Saccucci P, Cozzoli E, Cerminara C, Curatolo P, Bottini E. Gloria-Bottini F, et al. Among authors: curatolo p. Neuropediatrics. 2008 Dec;39(6):357-8. doi: 10.1055/s-0029-1202834. Epub 2009 Jun 30. Neuropediatrics. 2008. PMID: 19569003

4

Association of syndromic mental retardation and autism with 22q11.2 duplication.

Lo-Castro A, Galasso C, Cerminara C, El-Malhany N, Benedetti S, Nardone AM, Curatolo P. Lo-Castro A, et al. Among authors: curatolo p. Neuropediatrics. 2009 Jun;40(3):137-40. doi: 10.1055/s-0029-1237724. Epub 2009 Dec 17. Neuropediatrics. 2009. PMID: 20020400

5

Autism: evidence of association with adenosine deaminase genetic polymorphism.

Bottini N, De Luca D, Saccucci P, Fiumara A, Elia M, Porfirio MC, Lucarelli P, Curatolo P. Bottini N, et al. Among authors: curatolo p. Neurogenetics. 2001 Mar;3(2):111-3. doi: 10.1007/s100480000104. Neurogenetics. 2001. PMID: 11354825

6

Recent advances in the pathogenesis of syndromic autisms.

Benvenuto A, Manzi B, Alessandrelli R, Galasso C, Curatolo P. Benvenuto A, et al. Among authors: curatolo p. Int J Pediatr. 2009;2009:198736. doi: 10.1155/2009/198736. Epub 2009 Jun 21. Int J Pediatr. 2009. PMID: 19946417 Free PMC article.

7

Tourette syndrome and comorbid ADHD: causes and consequences.

El Malhany N, Gulisano M, Rizzo R, Curatolo P. El Malhany N, et al. Among authors: curatolo p. Eur J Pediatr. 2015 Mar;174(3):279-88. doi: 10.1007/s00431-014-2417-0. Epub 2014 Sep 17. Eur J Pediatr. 2015. PMID: 25224657 Review.

8

Diffuse polymicrogyria associated with congenital hydrocephalus, craniosynostosis, severe mental retardation, and minor facial and genital anomalies.

Pavone L, Rizzo R, Pavone P, Curatolo P, Dobyns WB. Pavone L, et al. Among authors: curatolo p. J Child Neurol. 2000 Jul;15(7):493-5. doi: 10.1177/088307380001500715. J Child Neurol. 2000. PMID: 10921525

9

Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophy.

Pavone L, Curatolo P, Rizzo R, Micali G, Incorpora G, Garg BP, Dunn DW, Dobyns WB. Pavone L, et al. Among authors: curatolo p. Neurology. 1991 Feb;41(2 ( Pt 1)):266-71. doi: 10.1212/wnl.41.2_part_1.266. Neurology. 1991. PMID: 1992373 Review.

10

ADHD and epilepsy in children with Tourette syndrome: a triple comorbidity?

Rizzo R, Gulisano M, Calì PV, Curatolo P. Rizzo R, et al. Among authors: curatolo p. Acta Paediatr. 2010 Dec;99(12):1894-6. doi: 10.1111/j.1651-2227.2010.01951.x. Epub 2010 Sep 27. Acta Paediatr. 2010. PMID: 21355881 No abstract available.

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