(Q50312318)

2 March 2018

title

Social impairments in Rett syndrome: characteristics and relationship with clinical severity (English)

1 reference

2 March 2018

0 references

W E Kaufmann

1 reference

2 March 2018

E Tierney

1 reference

2 March 2018

C A Rohde

1 reference

2 March 2018

M C Suarez-Pedraza

1 reference

2 March 2018

M A Clarke

1 reference

2 March 2018

C F Salorio

1 reference

2 March 2018

G Bibat

1 reference

2 March 2018

I Bukelis

1 reference

2 March 2018

D Naram

1 reference

2 March 2018

D C Lanham

1 reference

2 March 2018

S Naidu

1 reference

2 March 2018

publication date

8 March 2011

1 reference

2 March 2018

Journal of Intellectual Disability Research

published in

1 reference

2 March 2018

volume

1 reference

2 March 2018

issue

1 reference

2 March 2018

page(s)

233-247

1 reference

2 March 2018

Advances in autism genetics: on the threshold of a new neurobiology

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

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/10.1111%2FJ.1365-2788.2011.01404.X

Autistic-spectrum disorders in Down syndrome: further delineation and distinction from other behavioral abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Stereotypical hand movements in 144 subjects with Rett syndrome from the population-based Australian database.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Gross motor profile in rett syndrome as determined by video analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Early detection of social interaction problems: development of a social interaction instrument in young children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Clinical manifestations and stages of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Rett variants: a suggested model for inclusion criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Brain metabolism in Rett syndrome: age, clinical, and genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Motor-auditory-visual integration: The role of the human mirror neuron system in communication and communication disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

White matter impairment in Rett syndrome: diffusion tensor imaging study with clinical correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Rett syndrome in adults with severe intellectual disability: exploration of behavioral characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Features of autism in Rett syndrome and severe mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Towards a behavioral phenotype for Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Clinical variability in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Psychiatric disorders in children with autism spectrum disorders: prevalence, comorbidity, and associated factors in a population-derived sample

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Is Rett syndrome a subtype of pervasive developmental disorders?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

21 January 2018

Rett syndrome in Sweden

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Autistic disorder symptoms in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

The diagnosis of autism in a female: could it be Rett syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Preserved speech variants of the Rett syndrome: molecular and clinical analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

Study of MECP2 gene in Rett syndrome variants and autistic girls.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2011.01404.X

10.1111/J.1365-2788.2011.01404.X

21 January 2018

Identifiers

DOI

1 reference

2 March 2018

1 reference

2 March 2018