(Q35492515)

8 August 2017

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

1 reference

8 August 2017

0 references

J C Carter

1

1 reference

8 August 2017

D C Lanham

2

1 reference

8 August 2017

D Pham

3

1 reference

8 August 2017

G Bibat

4

1 reference

8 August 2017

S Naidu

5

1 reference

8 August 2017

W E Kaufmann

6

1 reference

8 August 2017

7 December 2007

1 reference

American Journal of Neuroradiology

8 August 2017

1 reference

8 August 2017

29

1 reference

8 August 2017

3

1 reference

8 August 2017

436-441

1 reference

Behavioral and anatomical abnormalities in Mecp2 mutant mice: a model for Rett syndrome.

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Neural correlates of modality-specific spatial extinction.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

The posterior parietal cortex: sensorimotor interface for the planning and online control of visually guided movements

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Motor functions of the parietal lobe

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Clinical variability in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

A voxel-based morphometric study of nondemented adults with Down Syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Neuropathology of Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Proton MR spectroscopy in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Methyl-CpG-binding protein 2 mutations in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Mutation screening in Rett syndrome patients.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Rett syndrome: a disorder affecting early brain growth

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Cyclooxygenase-2 expression during rat neocortical development and in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Automatic atlas-based volume estimation of human brain regions from MR images

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Neuroanatomy of Rett syndrome: a volumetric imaging study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Selective dendritic alterations in the cortex of Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Rett syndrome studies of natural history and search for a genetic marker

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Abnormal expression of microtubule-associated protein 2 (MAP-2) in neocortex in Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

On a unusual brain atrophy syndrome in hyperammonemia in childhood

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Cerebral blood flow and oxygen metabolism in the Rett syndrome

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Cerebellar and cerebral abnormalities in Rett syndrome: a quantitative MR analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

MECP2 mutations account for most cases of typical forms of Rett syndrome.

12 July 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Towards a behavioral phenotype for Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Refining the phenotype of common mutations in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Superior temporal sulcus anatomical abnormalities in childhood autism: a voxel-based morphometry MRI study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Quantitative magnetic resonance imaging in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Dendritic cytoskeletal protein expression in mental retardation: an immunohistochemical study of the neocortex in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Neural substrates of knowledge of hand postures for object grasping and functional object use: evidence from fMRI.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Is the early development of girls with Rett disorder really normal?

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

Automated Talairach atlas-based parcellation and measurement of cerebral lobes in children.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4403765

Parieto-occipital grey matter abnormalities in children with Williams syndrome

26 September 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A0857

MeCP2 mutations in children with and without the phenotype of Rett syndrome

21 January 2018

1 reference

12 December 2020

Regional cerebral blood flow abnormalities in Rett syndrome

1 reference

12 December 2020

Rett syndrome: a suggested staging system for describing impairment profile with increasing age towards adolescence

1 reference

12 December 2020

Influence of mutation type and location on phenotype in 123 patients with Rett syndrome

1 reference

12 December 2020

Clinical delineation of Rett syndrome variants

1 reference

12 December 2020

Rett syndrome--natural history in 70 cases

1 reference

12 December 2020

Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group

1 reference

12 December 2020

Quantitative 1H MR spectroscopic imaging in early Rett syndrome

1 reference

12 December 2020

Identifiers

DOI

10.3174/AJNR.A0857

1 reference

8 August 2017

1 reference

8 August 2017

1 reference