Pages that link to "Q52099826"
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The following pages link to Cognitive profiles associated with the fra(X) syndrome in males and females. (Q52099826):
Displaying 50 items.
- Behavioural phenotypes and special educational needs: is aetiology important in the classroom? (Q22242621) (← links)
- Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome (Q24613296) (← links)
- Prefrontal social cognition network dysfunction underlying face encoding and social anxiety in fragile X syndrome (Q24647484) (← links)
- From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment (Q27020947) (← links)
- Developing Medications Targeting Glutamatergic Dysfunction in Autism: Progress to Date (Q27025683) (← links)
- Normal Performance of Fmr1 Mice on a Touchscreen Delayed Nonmatching to Position Working Memory Task (Q30387508) (← links)
- Modeling fragile X syndrome in the Fmr1 knockout mouse (Q30420595) (← links)
- Cerebral growth in Fragile X syndrome: review and comparison with Down syndrome (Q30703355) (← links)
- Language Development in Individuals with Fragile X Syndrome (Q33788960) (← links)
- Biomarkers in the Study of Families of Individuals with Developmental Disabilities (Q33795272) (← links)
- Exceptional memory performance in the Long Life Family Study (Q33893228) (← links)
- The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neurons (Q34316545) (← links)
- Social functioning among girls with fragile X or Turner syndrome and their sisters (Q34490903) (← links)
- Different approaches to relating genotype to phenotype in developmental disorders (Q34561421) (← links)
- Cognitive Aspects of Fragile X syndrome (Q34626140) (← links)
- Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA. (Q34660995) (← links)
- Longitudinal changes in intellectual development in children with Fragile X syndrome (Q34762581) (← links)
- Insular volume reduction in fragile X syndrome (Q34984581) (← links)
- Oxytocin and vasopressin systems in genetic syndromes and neurodevelopmental disorders (Q35009426) (← links)
- Discrimination learning and attentional set formation in a mouse model of Fragile X (Q35027861) (← links)
- Visuospatial and numerical cognitive deficits in children with chromosome 22q11.2 deletion syndrome (Q35054138) (← links)
- Fragile x syndrome and autism: from disease model to therapeutic targets (Q35187269) (← links)
- Neurobehavioral effects of the fragile X premutation in adult women: a controlled study. (Q35194094) (← links)
- Neuroanatomy in fragile X females: the posterior fossa (Q35197149) (← links)
- Aberrant frontal lobe maturation in adolescents with fragile X syndrome is related to delayed cognitive maturation (Q35317895) (← links)
- Working memory subsystems and task complexity in young boys with Fragile X syndrome (Q35623084) (← links)
- DNA microarrays and animal models of learning and memory. (Q35913295) (← links)
- Examining the neural correlates of emergent equivalence relations in fragile X syndrome (Q36012007) (← links)
- Young adult male carriers of the fragile X premutation exhibit genetically modulated impairments in visuospatial tasks controlled for psychomotor speed (Q36423826) (← links)
- Cognitive, environmental, and linguistic predictors of syntax in fragile X syndrome and Down syndrome (Q36595789) (← links)
- Language development and fragile X syndrome: profiles, syndrome-specificity, and within-syndrome differences. (Q36746547) (← links)
- Contrast detection in infants with fragile X syndrome (Q36793835) (← links)
- Fragile X syndrome: Neural network models of sequencing and memory (Q36960248) (← links)
- Moving Toward Integrative, Multidimensional Research in Modern Psychiatry: Lessons Learned From Fragile X Syndrome (Q37018574) (← links)
- Chronological age, but not FMRP levels, predicts neuropsychological performance in girls with fragile X syndrome (Q37145945) (← links)
- Towards a neurodevelopmental model of clinical case formulation (Q37216245) (← links)
- Fragile-X: neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes (Q37369973) (← links)
- Insights into brain development from neurogenetic syndromes: evidence from fragile X syndrome, Williams syndrome, Turner syndrome and velocardiofacial syndrome (Q37450139) (← links)
- White matter microstructural abnormalities in girls with chromosome 22q11.2 deletion syndrome, Fragile X or Turner syndrome as evidenced by diffusion tensor imaging (Q37626841) (← links)
- Fragile X-associated disorders: a clinical overview. (Q37900184) (← links)
- The Role of Striatal-Enriched Protein Tyrosine Phosphatase (STEP) in Cognition (Q37921617) (← links)
- Interplay between synaptic endocannabinoid signaling and metaplasticity in neuronal circuit function and dysfunction (Q38203030) (← links)
- Drosophila fragile X mental retardation protein developmentally regulates activity-dependent axon pruning (Q38292954) (← links)
- Discourse processing in women with fragile x syndrome: evidence for a deficit establishing coherence (Q38554191) (← links)
- Fragile X syndrome -- from genes to cognition (Q39918863) (← links)
- Autism: the point of view from fragile X studies (Q40835732) (← links)
- Similarities in genetic mental retardation and neuroteratogenic syndromes (Q41290267) (← links)
- Screening for Fragile X Syndrome: Information Needs for Health Planners (Q41579814) (← links)
- The neuropsychology of mental retardation (Q41647190) (← links)
- Mental Retardation: A Review of the Past 10 Years. Part II (Q41662866) (← links)