about
L-acetylcarnitine for treating fragile X syndromeL-acetylcarnitine for fragile X syndromeFolic acid for fragile X syndromeFolic acid for fragile X syndromeImportance of Shank3 protein in regulating metabotropic glutamate receptor 5 (mGluR5) expression and signaling at synapsesOne world, one womanWhat can we learn about autism from studying fragile X syndrome?Emerging pharmacotherapies for neurodevelopmental disordersGroup 1 mGluR-dependent synaptic long-term depression: mechanisms and implications for circuitry and diseaseGenetics of autistic disorders: review and clinical implicationsFragile x syndromeSystematic review of pharmacological treatments in fragile X syndromeRNA Secondary Structure Modulates FMRP's Bi-Functional Role in the MicroRNA PathwayAdvances in the Understanding of the Gabaergic Neurobiology of FMR1 Expanded Alleles Leading to Targeted Treatments for Fragile X Spectrum DisorderEmerging pharmacologic treatment options for fragile X syndromeNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsFragile X syndrome as a rare disease in China - Therapeutic challenges and opportunitiesFragile X syndrome and targeted treatment trials.Fragile X syndromeDendritic spine dysgenesis in autism related disordersUnstable mutations in the FMR1 gene and the phenotypesThe contribution of inhibitory interneurons to circuit dysfunction in Fragile X SyndromeFragile X mental retardation protein regulates olfactory sensitivity but not odorant discriminationTherapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and BackFragile X syndrome: A review of clinical managementStudy of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 GeneThe neurobiology of the Prader-Willi phenotype of fragile X syndromeMOV10 and FMRP regulate AGO2 association with microRNA recognition elementsReduced gamma oscillations in a mouse model of intellectual disability: a role for impaired repetitive neurotransmission?Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486.Exploring the zebra finch Taeniopygia guttata as a novel animal model for the speech-language deficit of fragile X syndromeBehavioural phenotyping assays for mouse models of autismRole of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic Strategy.Degraded speech sound processing in a rat model of fragile X syndromePharmacological rescue of Ras signaling, GluA1-dependent synaptic plasticity, and learning deficits in a fragile X model.Fragile X: leading the way for targeted treatments in autism.Cardiovascular and behavioral response to auditory stimuli in boys with fragile X syndrome.Auditory processing in fragile x syndrome.Inhibition of spontaneous recovery of fear by mGluR5 after prolonged extinction trainingThe GABA(A) receptor agonist THIP ameliorates specific behavioral deficits in the mouse model of fragile X syndrome.
P2860
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Advances in the treatment of fragile X syndrome
@ast
Advances in the treatment of fragile X syndrome
@en
Advances in the treatment of fragile X syndrome
@nl
type
label
Advances in the treatment of fragile X syndrome
@ast
Advances in the treatment of fragile X syndrome
@en
Advances in the treatment of fragile X syndrome
@nl
prefLabel
Advances in the treatment of fragile X syndrome
@ast
Advances in the treatment of fragile X syndrome
@en
Advances in the treatment of fragile X syndrome
@nl
P2093
P2860
P3181
P356
P1433
P1476
Advances in the treatment of fragile X syndrome
@en
P2093
Ave Lachiewicz
Carol Delahunty
David Hessl
Elizabeth Berry-Kravis
Jeannie Visootsak
Jonathan Picker
Louise Gane
Michael Tranfaglia
Michele Y Ono
Nicole Tartaglia
P2860
P304
P3181
P356
10.1542/PEDS.2008-0317
P407
P577
2009-01-01T00:00:00Z