(Q34460527)

2 August 2017

1 reference

title

Importance of Rett syndrome in child neurology (English)

1 reference

2 August 2017

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Dunn HG

1

1 reference

2 August 2017

1 December 2001

1 reference

2 August 2017

Brain and Development

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2 August 2017

23 Suppl 1

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2 August 2017

S38-43

1 reference

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

2 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome--a review and discussion of syndrome delineation and syndrome definition.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Neuropathology of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Microscopic Observations of the Brain in Rett Syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett variants: a suggested model for inclusion criteria.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett's syndrome in the west of Scotland

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome in Sweden.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome, classical and atypical: genealogical support for common origin

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome: geographic variation in prevalence in Norway.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

A severely affected male born into a Rett syndrome kindred supports X-linked inheritance and allows extension of the exclusion map.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Molecular approaches to the Rett syndrome gene

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Breaking the silence in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Methyl-CpG-binding protein 2 mutations in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

The neuropathology of Rett syndrome--overview 1994.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Preliminary evidence for neurodegenerative changes in the substantia nigra of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Morphological study of neocortical areas in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett's syndrome. Correlation of electroencephalographic characteristics with clinical staging

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome: EEG presentation.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

EEG and respiration in Rett syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Unusual EEG theta rhythms over central region in Rett syndrome: considerations of the underlying dysfunction.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome: characterization of seizures versus non-seizures

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Cortical reflex myoclonus in Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Long-term mechanical ventilation in infants with neuromuscular disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Neurophysiological findings in the Rett syndrome, I: EMG, conduction velocity, EEG and somatosensory-evoked potential studies.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Anatomy of Rett syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Management of Rett syndrome: a ten year experience

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome: a disorder affecting early brain growth

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

SPECT of the brain in childhood autism: evidence for a lack of normal hemispheric asymmetry.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Developmental changes in brain serotonin synthesis capacity in autistic and nonautistic children.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

Neuroanatomy in Rett syndrome: cerebral cortex and posterior fossa

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900335-7

7 January 2021

10.1016/S0387-7604(01)00335-7

Identifiers

DOI

1 reference

2 August 2017

1 reference

PubMed ID

11738840