(Q41937674)

14 October 2017

title

Aicardi-Goutieres syndrome: neuroradiologic findings and follow-up (English)

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Aicardi-Goutieres syndrome

14 October 2017

main subject

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5

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14 October 2017

C Uggetti

1

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Elisa Fazzi

object named as

E Fazzi

6

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author name string

R La Piana

2

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14 October 2017

S Orcesi

3

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14 October 2017

M G Egitto

4

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14 October 2017

publication date

23 July 2009

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American Journal of Neuroradiology

14 October 2017

published in

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14 October 2017

volume

30

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14 October 2017

issue

10

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14 October 2017

page(s)

1971-1976

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

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

The natural history of Aicardi-Goutières syndrome: follow-up of 11 Italian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Aicardi-Goutières syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Clinical and molecular phenotype of Aicardi-Goutieres syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Aicardi-Goutieres syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Lack of progression of brain atrophy in Aicardi-Goutières syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Regression of white matter hypodensities with age in Aicardi-Goutierés syndrome: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Nucleic acid-mediated inflammatory diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Aicardi-Goutières syndrome: a genetic microangiopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Invited article: an MRI-based approach to the diagnosis of white matter disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3174%2FAJNR.A1694

Aicardi-Goutières syndrome: neuroradiological findings after nine years of follow-up

21 January 2018

1 reference

12 December 2020

The neuropathology of Aicardi-Goutières syndrome

1 reference

12 December 2020

Brain lactic alkalosis in Aicardi-Goutières syndrome.

1 reference

12 December 2020

Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?

1 reference

12 December 2020

Astrocytes produce interferon-alpha and CXCL10, but not IL-6 or CXCL8, in Aicardi-Goutières syndrome

1 reference

12 December 2020

Aicardi-Goutières syndrome: description of a late onset case

1 reference

12 December 2020

Congenital glaucoma and brain stem atrophy as features of Aicardi-Goutières syndrome.

1 reference

12 December 2020

Aicardi-Goutières syndrome: an important Mendelian mimic of congenital infection

1 reference

12 December 2020

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

1 reference

12 December 2020

Aicardi-Goutières syndrome: clinical and neuroradiological findings of 10 new cases.

1 reference

12 December 2020

Identifiers

DOI

10.3174/AJNR.A1694

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14 October 2017

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