(Q52858830)

9 May 2018

title

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

1 reference

9 May 2018

author

Yanick J. Crow

1

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9 May 2018

C Geoffrey Woods

6

object named as

C G Woods

1 reference

9 May 2018

author name string

R F Massey

2

1 reference

9 May 2018

J R Innes

3

1 reference

9 May 2018

P W Pairaudeau

4

1 reference

9 May 2018

C A Rowland Hill

5

1 reference

9 May 2018

M Ali

7

1 reference

9 May 2018

J H Livingston

8

1 reference

9 May 2018

P Lebon

9

1 reference

9 May 2018

K Nischall

10

1 reference

9 May 2018

M McEntagart

11

1 reference

9 May 2018

N Hindocha

12

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9 May 2018

R M Winter

13

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9 May 2018

language of work or name

English

0 references

publication date

1 September 2004

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9 May 2018

American Journal of Medical Genetics

published in

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9 May 2018

volume

129A

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9 May 2018

page(s)

303-307

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9 May 2018

issue

3

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9 May 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30250

Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30250

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30250

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/10.1002%2FAJMG.A.30250

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30250

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.A.30250

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.30250

1 reference

9 May 2018

PubMed ID

15326633

1 reference

9 May 2018