(Q40528228)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Maha Zaki

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

Nagwa Abdel Meguid

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

author name string

P Lebon

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

language of work or name

English

0 references

publication date

1 July 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

volume

93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

page(s)

929-936

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15303808%20AND%20SRC:MED&resulttype=core&format=json

A progressive familial encephalopathy in infancy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Cerebrospinal fluid pterins and folates in Aicardi-Goutières syndrome: a new phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Systemic Lupus Erythematosus or Aicardi-Goutières Syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Encephalitis among Cree children in northern Quebec

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome: a description of 21 new cases and a comparison with the literature.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Cree encephalitis is allelic with Aicardi-Goutiéres syndrome: implications for the pathogenesis of disorders of interferon alpha metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

The Aicardi-Goutières syndrome (familial, early onset encephalopathy with calcifications of the basal ganglia and chronic cerebrospinal fluid lymphocytosis).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome: special type early-onset encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome: an expanding phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

The Aircardi-Goutières syndrome: variable clinical expression in two siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Lack of progression of brain atrophy in Aicardi-Goutières syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Cerebral calcifications and cerebellar hypoplasia in two children: clinical, radiologic and neuropathological studies--a separate neurodevelopmental entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome displays genetic heterogeneity with one locus (AGS1) on chromosome 3p21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome: an update and results of interferon-alpha studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

A distinct difference in clinical expression of two siblings with Aicardi-Goutières syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X

Aicardi-Goutières syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1651-2227.2004.TB02691.X