Militerni R - Search Results

1

No evidence for association between dyslexia and DYX1C1 functional variants in a group of children and adolescents from Southern Italy.

Bellini G, Bravaccio C, Calamoneri F, Donatella Cocuzza M, Fiorillo P, Gagliano A, Mazzone D, del Giudice EM, Scuccimarra G, Militerni R, Pascotto A. Bellini G, et al. Among authors: militerni r. J Mol Neurosci. 2005;27(3):311-4. doi: 10.1385/jmn:27:3:311. J Mol Neurosci. 2005. PMID: 16280601

2

Repetitive behaviors in autistic disorder.

Militerni R, Bravaccio C, Falco C, Fico C, Palermo MT. Militerni R, et al. Eur Child Adolesc Psychiatry. 2002 Oct;11(5):210-8. doi: 10.1007/s00787-002-0279-x. Eur Child Adolesc Psychiatry. 2002. PMID: 12469238

3

Etiopathogenesis of autism spectrum disorders: fitting the pieces of the puzzle together.

Gentile I, Zappulo E, Militerni R, Pascotto A, Borgia G, Bravaccio C. Gentile I, et al. Among authors: militerni r. Med Hypotheses. 2013 Jul;81(1):26-35. doi: 10.1016/j.mehy.2013.04.002. Epub 2013 Apr 25. Med Hypotheses. 2013. PMID: 23622947

4

Alterations of the intestinal barrier in patients with autism spectrum disorders and in their first-degree relatives.

de Magistris L, Familiari V, Pascotto A, Sapone A, Frolli A, Iardino P, Carteni M, De Rosa M, Francavilla R, Riegler G, Militerni R, Bravaccio C. de Magistris L, et al. Among authors: militerni r. J Pediatr Gastroenterol Nutr. 2010 Oct;51(4):418-24. doi: 10.1097/MPG.0b013e3181dcc4a5. J Pediatr Gastroenterol Nutr. 2010. PMID: 20683204

5

Lack of association between serotonin transporter gene promoter variants and autistic disorder in two ethnically distinct samples.

Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Conciatori M, Damiani V, Baldi A, Keller F. Persico AM, et al. Among authors: militerni r. Am J Med Genet. 2000 Feb 7;96(1):123-7. Am J Med Genet. 2000. PMID: 10686565

6

Paraoxonase gene variants are associated with autism in North America, but not in Italy: possible regional specificity in gene-environment interactions.

D'Amelio M, Ricci I, Sacco R, Liu X, D'Agruma L, Muscarella LA, Guarnieri V, Militerni R, Bravaccio C, Elia M, Schneider C, Melmed R, Trillo S, Pascucci T, Puglisi-Allegra S, Reichelt KL, Macciardi F, Holden JJ, Persico AM. D'Amelio M, et al. Among authors: militerni r. Mol Psychiatry. 2005 Nov;10(11):1006-16. doi: 10.1038/sj.mp.4001714. Mol Psychiatry. 2005. PMID: 16027737

7

Serotonin transporter gene promoter variants do not explain the hyperserotoninemia in autistic children.

Persico AM, Pascucci T, Puglisi-Allegra S, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Rabinowitz D, Reichelt KL, Conciatori M, Marino R, Keller F. Persico AM, et al. Among authors: militerni r. Mol Psychiatry. 2002;7(7):795-800. doi: 10.1038/sj.mp.4001069. Mol Psychiatry. 2002. PMID: 12192626

8

Effect of different starting doses of levothyroxine on growth and intellectual outcome at four years of age in congenital hypothyroidism.

Salerno M, Militerni R, Bravaccio C, Micillo M, Capalbo D, Di MS, Tenore A. Salerno M, et al. Among authors: militerni r. Thyroid. 2002 Jan;12(1):45-52. doi: 10.1089/105072502753451968. Thyroid. 2002. PMID: 11838730

9

Intellectual outcome at 12 years of age in congenital hypothyroidism.

Salerno M, Militerni R, Di Maio S, Bravaccio C, Gasparini N, Tenore A. Salerno M, et al. Among authors: militerni r. Eur J Endocrinol. 1999 Aug;141(2):105-10. doi: 10.1530/eje.0.1410105. Eur J Endocrinol. 1999. PMID: 10427151

10

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: militerni r. Mol Psychiatry. 2009 Jul;14(7):705-18. doi: 10.1038/mp.2008.21. Epub 2008 Mar 4. Mol Psychiatry. 2009. PMID: 18317465

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