(Q37900184)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

review article

1 reference

title

Fragile X-associated disorders: a clinical overview (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

publication date

12 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

volume

259

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

page(s)

401-413

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-011-6161-3

7 February 2020

exact match

0 references

cites work

Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population

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Prevalence of the fragile X syndrome in African-Americans

21 January 2018

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The fragile X premutation: into the phenotypic fold

21 January 2018

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Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

21 January 2018

1 reference

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Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

21 January 2018

1 reference

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Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuropsychological dysfunction among affected heterozygous fragile X females

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Verbal learning and memory among heterozygous fragile X females

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X genotype characterized by an unstable region of DNA.

21 January 2018

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Profiling Fragile X Syndrome in males: strengths and weaknesses in cognitive abilities.

21 January 2018

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Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues

21 January 2018

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Fragile X: a family of disorders

21 January 2018

1 reference

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Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X syndrome, DSM-III-R, and autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Autistic behavior in children with fragile X syndrome: prevalence, stability, and the impact of FMRP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Autism spectrum disorder in fragile X syndrome: communication, social interaction, and specific behaviors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Behavioral relationship between autism and fragile x syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Brief report: aggression and stereotypic behavior in males with fragile X syndrome--moderating secondary genes in a "single gene" disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

A solution to limitations of cognitive testing in children with intellectual disabilities: the case of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Cognitive profiles associated with the fra(X) syndrome in males and females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Cognitive profiles and the spectrum of clinical manifestations in heterozygous fra (X) females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

A neuropsychological profile of attention deficits in young males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Empirical test of the Inglis and Lawson hypothesis about sex differences in WAIS and WAIS-R brain-damage studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

True precocious puberty in a girl with the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Phenotypic variation and FMRP levels in fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Mood and anxiety disorders in females with the FMR1 premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Psychiatric disability in female carriers of the fragile X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Transmitting males and carrier females in fragile X--revisited.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Behavioral and psychiatric disorders in adult male carriers of fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Clinical features of boys with fragile X premutations and intermediate alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Autistic spectrum disorder and the fragile X premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The emerging fragile X premutation phenotype: evidence from the domain of social cognition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Early development, temperament, and functional impairment in autism and fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Penetrance of FMR1 premutation associated pathologies in fragile X syndrome families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Anxiety and depression, attention, and executive functions in hypothyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Depression and anxiety in different thyroid function states

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The fragile X premutation presenting as essential tremor.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Expanded clinical phenotype of women with the FMR1 premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Lifespan changes in working memory in fragile X premutation males

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Premature ovarian failure in the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Elevated levels of FMR1 mRNA in carrier males: a new mechanism of involvement in the fragile-X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The RNA binding protein FMRP: new connections and missing links.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Knockout mouse model for Fxr2: a model for mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Translational complexity of the fragile x mental retardation protein: insights from the fly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Local functions for FMRP in axon growth cone motility and activity-dependent regulation of filopodia and spine synapses

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Expression profiling suggests underexpression of the GABA(A) receptor subunit delta in the fragile X knockout mouse model

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Attenuated sensitivity to neuroactive steroids in gamma-aminobutyrate type A receptor delta subunit knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Decreased expression of the GABAA receptor in fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Expression of the GABAergic system in animal models for fragile X syndrome and fragile X associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Synaptic regulation of protein synthesis and the fragile X protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Local protein synthesis and spine morphogenesis: Fragile X syndrome and beyond.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X: translation in action

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

The mGluR theory of fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Repetitive self-grooming behavior in the BTBR mouse model of autism is blocked by the mGluR5 antagonist MPEP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Treatment of anxiety using fenobam (a nonbenzodiazepine) in a double-blind standard (diazepam) placebo-controlled study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

A pilot open label, single dose trial of fenobam in adults with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Open-label add-on treatment trial of minocycline in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Analysis of neocortex in three males with the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Dendritic spine structural anomalies in fragile-X mental retardation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuroanatomical, molecular genetic, and behavioral correlates of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X mental retardation protein is required for synapse elimination by the activity-dependent transcription factor MEF2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neurodevelopmental effects of the FMR-1 full mutation in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Morphometric spatial patterns differentiating boys with fragile X syndrome, typically developing boys, and developmentally delayed boys aged 1 to 3 years

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Teasing apart the heterogeneity of autism: Same behavior, different brains in toddlers with fragile X syndrome and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

In vivo brain anatomy of adult males with Fragile X syndrome: an MRI study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

A voxel-based morphometry comparison of regional gray matter between fragile X syndrome and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Decreased cerebellar posterior vermis size in fragile X syndrome: correlation with neurocognitive performance

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuroanatomy of fragile X syndrome: the posterior fossa

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Neuroanatomy of fragile X syndrome: the temporal lobe

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Application of an automated parcellation method to the analysis of pediatric brain volumes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Differential impact of the FMR-1 full mutation on memory and attention functioning : a neuropsychological perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fronto-striatal dysfunction and potential compensatory mechanisms in male adolescents with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Attentional activation of the cerebellum independent of motor involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Persistent cognitive dysfunction secondary to cerebellar injury in patients treated for posterior fossa tumors in childhood.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Magnetic resonance imaging study in older fragile X premutation male carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Molecular and imaging correlates of the fragile X-associated tremor/ataxia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Reduced Hippocampal Activation During Recall is Associated with Elevated FMR1 mRNA and Psychiatric Symptoms in Men with the Fragile X Premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Amygdala dysfunction in men with the fragile X premutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

A quantitative ELISA assay for the fragile x mental retardation 1 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

Fragile X premutations in familial premature ovarian failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-6161-3

FMRP expression as a potential prognostic indicator in fragile X syndrome.

21 January 2018

1 reference

12 December 2020

An anthropometric study of males with the fragile-X syndrome

1 reference

12 December 2020

The neurocognitive phenotype of female carriers of fragile X: additional evidence for specificity.

1 reference

12 December 2020

Chemical induction of mGluR5- and protein synthesis--dependent long-term depression in hippocampal area CA1.

1 reference

12 December 2020

Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome

1 reference

12 December 2020

Neuropsychiatric Aspects of Fragile X Syndrome.

1 reference

12 December 2020

Psychiatric disorders associated with fragile X in the young female.

1 reference

12 December 2020

Clinical features and reproductive patterns in fragile X female heterozygotes

1 reference

12 December 2020

Phenotypic involvement in females with the FMR1 gene mutation.

1 reference

12 December 2020

Nature of the working memory deficit in fragile-X syndrome.

1 reference

12 December 2020

Aberrant behaviors of young boys with fragile X syndrome.

1 reference

12 December 2020

Genetic and environmental influences on the cognitive outcomes of children with fragile X syndrome

1 reference

12 December 2020

Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome.

1 reference

12 December 2020

Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome.

1 reference

12 December 2020

Strengths and weaknesses in the intellectual functioning of males with fragile X syndrome.

1 reference

12 December 2020

Fragile X syndrome. Clinical, electroencephalographic and neuroimaging characteristics.

1 reference

12 December 2020

Fragile X syndrome: diagnostic and carrier testing. Working Group of the Genetic Screening Subcommittee of the Clinical Practice Committee. American College of Medical Genetics

1 reference

12 December 2020

Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

1 reference

12 December 2020

Autism profiles of males with fragile X syndrome

1 reference

12 December 2020

Adult fragile X syndrome: neuropsychology, brain anatomy, and metabolism.

1 reference

12 December 2020

Role for Rapid Dendritic Protein Synthesis in Hippocampal mGluR-Dependent Long-Term Depression

1 reference

12 December 2020

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization

1 reference

12 December 2020

A controlled trial of stimulant medication in children with the fragile X syndrome

1 reference

12 December 2020

Molecular-clinical correlations in males with an expanded FMR1 mutation

1 reference

12 December 2020

Girls with fragile X syndrome: physical and neurocognitive status and outcome

1 reference

12 December 2020

Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary data

1 reference

12 December 2020

A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome.

1 reference

12 December 2020

Epilepsy in fragile X syndrome.

1 reference

12 December 2020

Spatial attention deficits in patients with acquired or developmental cerebellar abnormality

1 reference

12 December 2020

Autistic behavior in young boys with fragile X syndrome.

1 reference

12 December 2020

Fragile X syndrome and selective mutism.

1 reference

12 December 2020

Molecular insights into mental retardation: multiple functions for the Fragile X mental retardation protein?

1 reference

12 December 2020

Fragile X premutation carriers: characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction.

1 reference

12 December 2020

The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2

1 reference

12 December 2020

Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers.

1 reference

12 December 2020

The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals

1 reference

12 December 2020

A marker X chromosome

1 reference

12 December 2020

Prenatal diagnosis of fragile X syndrome

1 reference

12 December 2020

Spatial cognition in males with Fragile-X syndrome: evidence for a neuropsychological phenotype.

1 reference

12 December 2020

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

12 December 2020

Screening for fragile X syndrome in women of reproductive age

1 reference

12 December 2020

Learning-disabled males with a fragile X CGG expansion in the upper premutation size range.

1 reference

12 December 2020

Learning disabilities and attentional problems in boys with the fragile X syndrome.

1 reference

12 December 2020

A review of fragile X premutation disorders: expanding the psychiatric perspective

1 reference

12 December 2020

10.1007/S00415-011-6161-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21748281%20AND%20SRC:MED&resulttype=core&format=json

7 February 2020

1 reference