Militerni R - Search Results

1

A novel mutation in the CLN1 gene in a patient with juvenile neuronal ceroid lipofuscinosis.

Mazzei R, Conforti FL, Magariello A, Bravaccio C, Militerni R, Gabriele AL, Sampaolo S, Patitucci A, Di Iorio G, Muglia M, Quattrone A. Mazzei R, et al. Among authors: militerni r. J Neurol. 2002 Oct;249(10):1398-400. doi: 10.1007/s00415-002-0849-3. J Neurol. 2002. PMID: 12382155

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

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

4

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

5

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

6

No association between the 4g/5G polymorphism of the plasminogen activator inhibitor-1 gene promoter and autistic disorder.

Persico AM, Militerni R, Bravaccio C, Schneider C, Melmed R, Trillo S, Montecchi F, Palermo M, Pascucci T, Puglisi-Allegra S, Reichelt KL, Conciatori M, Keller F. Persico AM, et al. Among authors: militerni r. Psychiatr Genet. 2001 Jun;11(2):99-103. doi: 10.1097/00041444-200106000-00008. Psychiatr Genet. 2001. PMID: 11525425

7

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

8

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

9

Association between the HOXA1 A218G polymorphism and increased head circumference in patients with autism.

Conciatori M, Stodgell CJ, Hyman SL, O'Bara M, Militerni R, Bravaccio C, Trillo S, Montecchi F, Schneider C, Melmed R, Elia M, Crawford L, Spence SJ, Muscarella L, Guarnieri V, D'Agruma L, Quattrone A, Zelante L, Rabinowitz D, Pascucci T, Puglisi-Allegra S, Reichelt KL, Rodier PM, Persico AM. Conciatori M, et al. Among authors: militerni r. Biol Psychiatry. 2004 Feb 15;55(4):413-9. doi: 10.1016/j.biopsych.2003.10.005. Biol Psychiatry. 2004. PMID: 14960295

10

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: militerni r. Mol Autism. 2010 May 25;1(1):9. doi: 10.1186/2040-2392-1-9. Mol Autism. 2010. PMID: 20678259 Free PMC article.

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