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English
Rett syndrome: exploring the autism link
scientific article published on August 2011
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Rett syndrome: exploring the autism link
(English)
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
main subject
autism
0 references
Rett syndrome
0 references
author
Alan K. Percy
series ordinal
1
object named as
Alan K Percy
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
language of work or name
English
1 reference
based on heuristic
inferred from title
publication date
1 August 2011
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
number of pages
5
1 reference
based on heuristic
inferred from page(s)
published in
Archives of Neurology
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
volume
68
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
issue
8
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
page(s)
985-989
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
cites work
Rett syndrome: revised diagnostic criteria and nomenclature
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Epilepsy and the natural history of Rett syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Repetitive self-grooming behavior in the BTBR mouse model of autism is blocked by the mGluR5 antagonist MPEP.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Profiling scoliosis in Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Longevity in Rett syndrome: analysis of the North American Database
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
MeCP2, a key contributor to neurological disease, activates and represses transcription
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Reversal of neurological defects in a mouse model of Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
29 September 2017
Early progressive encephalopathy in boys and MECP2 mutations
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
27 June 2018
Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
4 September 2018
Neonatal encephalopathy in two boys in families with recurrent Rett syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
4 September 2018
Review of Rett syndrome.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3674963
retrieved
4 September 2018
Identifiers
DOI
10.1001/ARCHNEUROL.2011.149
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
PMCID
3674963
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
PubMed ID
21825235
1 reference
stated in
Europe PubMed Central
PMCID
3674963
retrieved
17 August 2017
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