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Page 1
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: manzi b. BMC Med Genet. 2007 Mar 8;8:11. doi: 10.1186/1471-2350-8-11. BMC Med Genet. 2007. PMID: 17346350 Free PMC article.
Autism in tuberous sclerosis.
Curatolo P, Porfirio MC, Manzi B, Seri S. Curatolo P, et al. Among authors: manzi b. 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: manzi b. 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. J Child Neurol. 2008 Mar;23(3):307-14. doi: 10.1177/0883073807308698. Epub 2007 Dec 13. J Child Neurol. 2008. PMID: 18079313 Review.
Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression.
Lintas C, Sacco R, Garbett K, Mirnics K, Militerni R, Bravaccio C, Curatolo P, Manzi B, Schneider C, Melmed R, Elia M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Lintas C, et al. Among authors: manzi b. Mol Psychiatry. 2009 Jul;14(7):705-18. doi: 10.1038/mp.2008.21. Epub 2008 Mar 4. Mol Psychiatry. 2009. PMID: 18317465
Altered calcium homeostasis in autism-spectrum disorders: evidence from biochemical and genetic studies of the mitochondrial aspartate/glutamate carrier AGC1.
Palmieri L, Papaleo V, Porcelli V, Scarcia P, Gaita L, Sacco R, Hager J, Rousseau F, Curatolo P, Manzi B, Militerni R, Bravaccio C, Trillo S, Schneider C, Melmed R, Elia M, Lenti C, Saccani M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Persico AM. Palmieri L, et al. Among authors: manzi b. Mol Psychiatry. 2010 Jan;15(1):38-52. doi: 10.1038/mp.2008.63. Epub 2008 Jul 8. Mol Psychiatry. 2010. PMID: 18607376
Syndromic autism: causes and pathogenetic pathways.
Benvenuto A, Moavero R, Alessandrelli R, Manzi B, Curatolo P. Benvenuto A, et al. Among authors: manzi b. 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.
Recent advances in the pathogenesis of syndromic autisms.
Benvenuto A, Manzi B, Alessandrelli R, Galasso C, Curatolo P. Benvenuto A, et al. Among authors: manzi b. Int J Pediatr. 2009;2009:198736. doi: 10.1155/2009/198736. Epub 2009 Jun 21. Int J Pediatr. 2009. PMID: 19946417 Free PMC article.
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: manzi b. 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
33 results