(Q42506375)

1 November 2017

title

Congenital fibrosis of the extraocular muscles associated with cortical dysplasia and maldevelopment of the basal ganglia (English)

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congenital fibrosis of the extraocular muscles

1 November 2017

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author name string

Flaherty MP

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1 November 2017

Grattan-Smith P

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1 November 2017

Steinberg A

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1 November 2017

Jamieson R

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1 November 2017

Engle EC

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1 November 2017

publication date

1 July 2001

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1 November 2017

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1 November 2017

volume

108

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1 November 2017

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1 November 2017

page(s)

1313-1322

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Congenital fibrosis of the extraocular muscles; a report of six cases

1 November 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Phenotypic heterogeneity may occur in congenital fibrosis of the extraocular muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Hereditary congenital external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Mapping a gene for congenital fibrosis of the extraocular muscles to the centromeric region of chromosome 12.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Oculomotor nerve and muscle abnormalities in congenital fibrosis of the extraocular muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Hereditary external ophthalmoplegia synergistic divergence, jaw winking, and oculocutaneous hypopigmentation: a congenital fibrosis syndrome caused by deficient innervation to extraocular muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Congenital familial external ophthalmoplegia with co-contraction

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Joubert's syndrome associated with congenital ocular fibrosis and histidinemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Neurological impairment in congenital bilateral ptosis with ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Bilateral congenital restriction of upward eye movement

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Congenital unilateral fibrosis, blepharoptosis, and enophthalmos syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

Congenital fibrosis of the vertically acting extraocular muscles. A new group of dominantly inherited ocular fibrosis with radiologic findings

1 reference

https://api.crossref.org/works/10.1016%2FS0161-6420%2801%2900582-6

7 January 2021

10.1016/S0161-6420(01)00582-6

Identifiers

DOI

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1 November 2017

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