Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
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Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.Degraded neural and behavioral processing of speech sounds in a rat model of Rett syndrome.Automatic cortical representation of auditory pitch changes in Rett syndrome.Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.Profiling early socio-communicative development in five young girls with the preserved speech variant of Rett syndromeContributing to the early detection of Rett syndrome: the potential role of auditory Gestalt perceptionPreclinical research in Rett syndrome: setting the foundation for translational success.Safety, pharmacokinetics, and preliminary assessment of efficacy of mecasermin (recombinant human IGF-1) for the treatment of Rett syndrome.Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.Complexities of Rett syndrome and MeCP2Anxiety-like behavior in Rett syndrome: characteristics and assessment by anxiety scales.Peculiarities in the gestural repertoire: an early marker for Rett syndrome?The relationship of Rett syndrome and MECP2 disorders to autism.Changing the perspective on early development of Rett syndromeTraining communication abilities in Rett Syndrome through reading and writing.Brief report: MECP2 mutations in people without Rett syndrome.Neurobiologically-based treatments in Rett syndrome: opportunities and challenges.Translational research: Rett syndrome and tuberous sclerosis complex.Development of the Tailored Rett Intervention and Assessment Longitudinal (TRIAL) database and the Rett Evaluation of Symptoms and Treatments (REST) Questionnaire.Variations of stereotypies in individuals with Rett syndrome: A nationwide cross-sectional study in Taiwan.Modeling Williams syndrome with induced pluripotent stem cells.Social-emotional instability in individuals with Rett syndrome: parents' experiences with second stage behaviour.Developmental profile of speech-language and communicative functions in an individual with the preserved speech variant of Rett syndrome.Prevalence and associated features of depression in women with Rett syndrome.Adverse health in parents of children with disabilities and chronic health conditions: a meta-analysis using the parenting stress index's health sub-domain.Rett syndrome: an eye-tracking study of attention and recognition memory.Comparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life.MeCP2 R168X male and female mutant mice exhibit Rett-like behavioral deficits.Early socio-communicative forms and functions in typical Rett syndrome.Defining Hand Stereotypies in Rett Syndrome: A Movement Disorders Perspective.Co-occurrence of Dystonic and Dyskinetic Tongue Movements with Oral Apraxia in Post-regression Dysphagia in Classical Rett Syndrome Years of Life 1 Through 5.
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P2860
Social impairments in Rett syndrome: characteristics and relationship with clinical severity.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Social impairments in Rett syn ...... onship with clinical severity.
@en
Social impairments in Rett syn ...... onship with clinical severity.
@nl
type
label
Social impairments in Rett syn ...... onship with clinical severity.
@en
Social impairments in Rett syn ...... onship with clinical severity.
@nl
prefLabel
Social impairments in Rett syn ...... onship with clinical severity.
@en
Social impairments in Rett syn ...... onship with clinical severity.
@nl
P2093
P2860
P1476
Social impairments in Rett syn ...... onship with clinical severity.
@en
P2093
C F Salorio
D C Lanham
M A Clarke
M C Suarez-Pedraza
P2860
P304
P356
10.1111/J.1365-2788.2011.01404.X
P577
2011-03-08T00:00:00Z