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452 results

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Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.
Sacco R, Papaleo V, Hager J, Rousseau F, Moessner R, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Curatolo P, Manzi B, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Sacco R, et al. Among authors: curatolo p. BMC Med Genet. 2007 Mar 8;8:11. doi: 10.1186/1471-2350-8-11. BMC Med Genet. 2007. PMID: 17346350 Free PMC article.
Two-loci ADA haplotypes in autistic disorder.
Lucarelli P, Saccucci P, Bottini N, De Luca D, Fiumara A, Elia M, Bottini N, Porfirio MC, Curatolo P. Lucarelli P, et al. Among authors: curatolo p. Am J Med Genet. 2002 Apr 1;108(4):339-40. doi: 10.1002/ajmg.10272. Am J Med Genet. 2002. PMID: 11920843 No abstract available.
Association study of autistic disorder and chromosome 16p.
Lucarelli P, Palminiello S, Saccucci P, Bottini N, De Luca D, Elia M, Fiumara A, Curatolo P. Lucarelli P, et al. Among authors: curatolo p. Am J Med Genet A. 2003 Jun 1;119A(2):242-6. doi: 10.1002/ajmg.a.10187. Am J Med Genet A. 2003. PMID: 12749074 No abstract available.
Autism in tuberous sclerosis.
Curatolo P, Porfirio MC, Manzi B, Seri S. Curatolo P, et al. Eur J Paediatr Neurol. 2004;8(6):327-32. doi: 10.1016/j.ejpn.2004.08.005. Eur J Paediatr Neurol. 2004. PMID: 15542389 Review.
Clinical, morphological, and biochemical correlates of head circumference in autism.
Sacco R, Militerni R, Frolli A, Bravaccio C, Gritti A, Elia M, Curatolo P, Manzi B, Trillo S, Lenti C, Saccani M, Schneider C, Melmed R, Reichelt KL, Pascucci T, Puglisi-Allegra S, Persico AM. Sacco R, et al. Among authors: curatolo p. Biol Psychiatry. 2007 Nov 1;62(9):1038-47. doi: 10.1016/j.biopsych.2007.04.039. Epub 2007 Jul 20. Biol Psychiatry. 2007. PMID: 17644070
Autism and metabolic diseases.
Manzi B, Loizzo AL, Giana G, Curatolo P. Manzi B, et al. Among authors: curatolo p. J Child Neurol. 2008 Mar;23(3):307-14. doi: 10.1177/0883073807308698. Epub 2007 Dec 13. J Child Neurol. 2008. PMID: 18079313 Review.
Syndromic autism: causes and pathogenetic pathways.
Benvenuto A, Moavero R, Alessandrelli R, Manzi B, Curatolo P. Benvenuto A, et al. Among authors: curatolo p. World J Pediatr. 2009 Aug;5(3):169-76. doi: 10.1007/s12519-009-0033-2. Epub 2009 Aug 20. World J Pediatr. 2009. PMID: 19693459 Review.
Decreased serum arylesterase activity in autism spectrum disorders.
Gaita L, Manzi B, Sacco R, Lintas C, Altieri L, Lombardi F, Pawlowski TL, Redman M, Craig DW, Huentelman MJ, Ober-Reynolds S, Brautigam S, Melmed R, Smith CJ, Marsillach J, Camps J, Curatolo P, Persico AM. Gaita L, et al. Among authors: curatolo p. Psychiatry Res. 2010 Dec 30;180(2-3):105-13. doi: 10.1016/j.psychres.2010.04.010. Epub 2010 May 21. Psychiatry Res. 2010. PMID: 20488557
Candidate gene study of HOXB1 in autism spectrum disorder.
Muscarella LA, Guarnieri V, Sacco R, Curatolo P, Manzi B, Alessandrelli R, Giana G, Militerni R, Bravaccio C, Lenti C, Saccani M, Schneider C, Melmed R, D'Agruma L, Persico AM. Muscarella LA, et al. Among authors: curatolo p. Mol Autism. 2010 May 25;1(1):9. doi: 10.1186/2040-2392-1-9. Mol Autism. 2010. PMID: 20678259 Free PMC article.
452 results