(Q34177694)

31 July 2017

A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification (English)

1 reference

https://api.crossref.org/works/10.1038/EYE.1988.56

31 July 2017

1 reference

6 January 2023

author name string

Tolmie JL

1

1 reference

31 July 2017

Browne BH

2

1 reference

31 July 2017

McGettrick PM

3

1 reference

31 July 2017

Stephenson JB

4

1 reference

31 July 2017

language of work or name

1 reference

1 January 1988

1 reference

full work available at URL

31 July 2017

http://www.nature.com/articles/eye198856.pdf

file format

Portable Document Format

1 reference

https://api.crossref.org/works/10.1038/EYE.1988.56

http://www.nature.com/articles/eye198856

6 January 2023

1 reference

https://api.crossref.org/works/10.1038/EYE.1988.56

6 January 2023

1 reference

31 July 2017

2 ( Pt 3)

1 reference

31 July 2017

297-303

1 reference

https://scigraph.springernature.com/pub.10.1038/eye.1988.56

31 July 2017

0 references

cites work

Coats's disease: definition and pathogenesis

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Coats' disease. Evaluation of management

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

COATS'S DISEASE. I. REVIEW OF THE LITERATURE, DIAGNOSTIC CRITERIA, CLINICAL FINDINGS, AND PLASMA LIPID STUDIES

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Bilateral Coats' disease in an infant (a clinical, angiographic, light and electron microscopic study).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Facioscapulohumeral dystrophy associated with hearing loss and Coats syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

Inflammatory facioscapulohumeral muscular dystrophy and Coats syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

7 January 2021

Retinal telangiectasia associated with hypogammaglobulinemia

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

7 January 2021

A syndrome with intracranial calcification and microcephaly in two sibs, resembling intrauterine infection

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

7 January 2021

Microcephaly and intracranial calcification in two brothers.

1 reference

https://api.crossref.org/works/10.1038%2FEYE.1988.56

7 January 2021

Identifiers

DOI

10.1038/EYE.1988.56

1 reference

Dimensions Publication ID

31 July 2017

0 references

1 reference