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Results: 1 to 20 of 30

1.

Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.

Tordjman S, Somogyi E, Coulon N, Kermarrec S, Cohen D, Bronsard G, Bonnot O, Weismann-Arcache C, Botbol M, Lauth B, Ginchat V, Roubertoux P, Barburoth M, Kovess V, Geoffray MM, Xavier J.

Front Psychiatry. 2014 Aug 4;5:53. doi: 10.3389/fpsyt.2014.00053. eCollection 2014. Review.

PMID:
25136320
[PubMed]
Free PMC Article
2.

CYFIP family proteins between autism and intellectual disability: links with Fragile X syndrome.

Abekhoukh S, Bardoni B.

Front Cell Neurosci. 2014 Mar 27;8:81. doi: 10.3389/fncel.2014.00081. eCollection 2014. Review.

PMID:
24733999
[PubMed]
Free PMC Article
3.

Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.

Doll CA, Broadie K.

Front Cell Neurosci. 2014 Feb 7;8:30. doi: 10.3389/fncel.2014.00030. eCollection 2014. Review.

PMID:
24570656
[PubMed]
Free PMC Article
4.

The role of ionotropic glutamate receptors in childhood neurodevelopmental disorders: autism spectrum disorders and fragile x syndrome.

Uzunova G, Hollander E, Shepherd J.

Curr Neuropharmacol. 2014 Jan;12(1):71-98. doi: 10.2174/1570159X113116660046.

PMID:
24533017
[PubMed]
Free PMC Article
5.

Pediatric psychopharmacology: too much or too little?

Rapoport JL.

World Psychiatry. 2013 Jun;12(2):118-23. doi: 10.1002/wps.20028.

PMID:
23737413
[PubMed]
Free PMC Article
6.

A randomized double-blind, placebo-controlled trial of minocycline in children and adolescents with fragile x syndrome.

Leigh MJ, Nguyen DV, Mu Y, Winarni TI, Schneider A, Chechi T, Polussa J, Doucet P, Tassone F, Rivera SM, Hessl D, Hagerman RJ.

J Dev Behav Pediatr. 2013 Apr;34(3):147-55. doi: 10.1097/DBP.0b013e318287cd17.

PMID:
23572165
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Unstable mutations in the FMR1 gene and the phenotypes.

Loesch D, Hagerman R.

Adv Exp Med Biol. 2012;769:78-114. Review.

PMID:
23560306
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Multiple autism-linked genes mediate synapse elimination via proteasomal degradation of a synaptic scaffold PSD-95.

Tsai NP, Wilkerson JR, Guo W, Maksimova MA, DeMartino GN, Cowan CW, Huber KM.

Cell. 2012 Dec 21;151(7):1581-94. doi: 10.1016/j.cell.2012.11.040.

PMID:
23260144
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Translational Concepts of mGluR5 in Synaptic Diseases of the Brain.

Piers TM, Kim DH, Kim BC, Regan P, Whitcomb DJ, Cho K.

Front Pharmacol. 2012 Nov 27;3:199. doi: 10.3389/fphar.2012.00199. eCollection 2012.

PMID:
23205012
[PubMed]
Free PMC Article
10.

The behavioral phenotype in MECP2 duplication syndrome: a comparison with idiopathic autism.

Peters SU, Hundley RJ, Wilson AK, Warren Z, Vehorn A, Carvalho CM, Lupski JR, Ramocki MB.

Autism Res. 2013 Feb;6(1):42-50. doi: 10.1002/aur.1262. Epub 2012 Nov 20.

PMID:
23169761
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Brief Report: social disability in autism spectrum disorder: results from Research Units on Pediatric Psychopharmacology (RUPP) Autism Network trials.

Scahill L, Hallett V, Aman MG, McDougle CJ, Eugene Arnold L, McCracken JT, Tierney E, Deng Y, Dziura J, Vitiello B; Research Units on Pediatric Psychopharmacology (RUPP) Autism Network).

J Autism Dev Disord. 2013 Mar;43(3):739-46. doi: 10.1007/s10803-012-1689-3.

PMID:
23104617
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Autism-associated mutations in ProSAP2/Shank3 impair synaptic transmission and neurexin-neuroligin-mediated transsynaptic signaling.

Arons MH, Thynne CJ, Grabrucker AM, Li D, Schoen M, Cheyne JE, Boeckers TM, Montgomery JM, Garner CC.

J Neurosci. 2012 Oct 24;32(43):14966-78. doi: 10.1523/JNEUROSCI.2215-12.2012.

PMID:
23100419
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Matrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome.

Siller SS, Broadie K.

Neural Plast. 2012;2012:124548. doi: 10.1155/2012/124548. Epub 2012 May 20. Review.

PMID:
22685676
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Drug development in pediatric psychiatry: current status, future trends.

March JS, Fegert JM.

Child Adolesc Psychiatry Ment Health. 2012 Feb 7;6:7. doi: 10.1186/1753-2000-6-7. No abstract available.

PMID:
22313578
[PubMed]
Free PMC Article
15.

Disrupted Homer scaffolds mediate abnormal mGluR5 function in a mouse model of fragile X syndrome.

Ronesi JA, Collins KA, Hays SA, Tsai NP, Guo W, Birnbaum SG, Hu JH, Worley PF, Gibson JR, Huber KM.

Nat Neurosci. 2012 Jan 22;15(3):431-40, S1. doi: 10.1038/nn.3033.

PMID:
22267161
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Caregiver opinions about fragile X population screening.

Bailey DB Jr, Bishop E, Raspa M, Skinner D.

Genet Med. 2012 Jan;14(1):115-21. doi: 10.1038/gim.0b013e31822ebaa6. Epub 2011 Sep 13.

PMID:
22237440
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Mutations causing syndromic autism define an axis of synaptic pathophysiology.

Auerbach BD, Osterweil EK, Bear MF.

Nature. 2011 Nov 23;480(7375):63-8. doi: 10.1038/nature10658.

PMID:
22113615
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Fragile x syndrome.

McLennan Y, Polussa J, Tassone F, Hagerman R.

Curr Genomics. 2011 May;12(3):216-24. doi: 10.2174/138920211795677886.

PMID:
22043169
[PubMed]
Free PMC Article
19.

Parkinson's disease therapeutics: new developments and challenges since the introduction of levodopa.

Smith Y, Wichmann T, Factor SA, DeLong MR.

Neuropsychopharmacology. 2012 Jan;37(1):213-46. doi: 10.1038/npp.2011.212. Epub 2011 Sep 28. Review.

PMID:
21956442
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Allosteric modulation of metabotropic glutamate receptors.

Sheffler DJ, Gregory KJ, Rook JM, Conn PJ.

Adv Pharmacol. 2011;62:37-77. doi: 10.1016/B978-0-12-385952-5.00010-5. Review.

PMID:
21907906
[PubMed - indexed for MEDLINE]
Free PMC Article

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