(Q35009216)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

review article

1 reference

title

Biogenic amines in Rett syndrome: the usual suspects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

Laurent Villard

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

author name string

Jean-Christophe Roux

series ordinal

1

1 reference

5 August 2017

language of work or name

English

0 references

publication date

23 October 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

volume

40

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

page(s)

59-75

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

Quantitative magnetic resonance imaging in Rett syndrome

10 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

Reduced folate transport to the CNS in female Rett patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

Altered neurochemical markers in Rett's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10519-009-9303-Y

10.1007/S10519-009-9303-Y

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19851857%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference