(Q34455774)

2 August 2017

Seizures in Rett syndrome: an overview from a one-year calendar study (English)

1 reference

2 August 2017

0 references

Le Jian

1

0 references

John Christodoulou

object named as

John Christodoulou

5

0 references

Nicholas de Klerk

object named as

Nicholas de Klerk

3

0 references

author name string

Lakshmi Nagarajan

2

1 reference

2 August 2017

David Ravine

4

1 reference

2 August 2017

Helen Leonard

6

1 reference

2 August 2017

language of work or name

1 reference

11 April 2007

1 reference

European Journal of Paediatric Neurology

2 August 2017

1 reference

2 August 2017

11

1 reference

2 August 2017

310-317

1 reference

2 August 2017

5

1 reference

Predictors of seizure onset in Rett syndrome.

2 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Rett syndrome in Australia: a review of the epidemiology.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Genotype and early development in Rett syndrome: the value of international data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Health service use in Rett syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Describing the phenotype in Rett syndrome using a population database

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Characterisation of breathing and associated central autonomic dysfunction in the Rett disorder

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Guidelines for reporting clinical features in cases with MECP2 mutations.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Predictors of scoliosis in Rett syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Vagus nerve stimulation for treatment of epilepsy in Rett syndrome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Effect of topiramate on seizures and respiratory dysrhythmia in Rett syndrome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Refining the phenotype of common mutations in Rett syndrome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Functional status of school-aged children with Down syndrome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Rett syndrome in Spain: mutation analysis and clinical correlations.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Epilepsy in a representative series of Rett syndrome.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Lamotrigine in Rett syndrome: treatment experience from a pilot study.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013620

Continuing Positive Secular Growth Change in the Netherlands 1955–1997

27 October 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Evaluation of the accuracy of seizure descriptions by the relatives of patients with epilepsy

1 reference

12 December 2020

An update on clinically applicable diagnostic criteria in Rett syndrome. Comments to Rett Syndrome Clinical Criteria Consensus Panel Satellite to European Paediatric Neurology Society Meeting, Baden Baden, Germany, 11 September 2001

1 reference

12 December 2020

Ketogenic diet in Rett syndrome

1 reference

12 December 2020

Rett syndrome in females with CTS hot spot deletions: a disorder profile

1 reference

12 December 2020

10.1016/J.EJPN.2007.02.008

Identifiers

DOI

1 reference

2 August 2017

1 reference

2 August 2017

1 reference