(Q37162573)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

review article

1 reference

title

Severe congenital encephalopathy caused by MECP2 null mutations in males: central hypoxia and reduced neuronal dendritic structure (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

0 references

0 references

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

author name string

B Schüle

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

D D Armstrong

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

A Oviedo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

U Francke

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

publication date

8 May 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

volume

74

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

page(s)

116-126

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01005.X

Quantitative immunohistochemistry of synaptophysin in human neocortex: an alternative method to estimate density of presynaptic terminals in paraffin sections

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01005.X

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01005.X

Occurrence of Rett syndrome in boys.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01005.X

MECP2 mutation analysis in patients with mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2008.01005.X

10.1111/J.1399-0004.2008.01005.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18477000%20AND%20SRC:MED&resulttype=core&format=json

7 January 2020

1 reference