(Q47895411)

6 February 2018

title

Visual function in children with merosin-deficient and merosin-positive congenital muscular dystrophy (English)

1 reference

6 February 2018

author name string

Mercuri E

1

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6 February 2018

Anker S

2

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6 February 2018

Philpot J

3

1 reference

6 February 2018

Sewry C

4

1 reference

6 February 2018

Dubowitz V

5

1 reference

6 February 2018

Muntoni F

6

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6 February 2018

publication date

1 May 1998

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6 February 2018

published in

Pediatric Neurology

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6 February 2018

volume

18

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6 February 2018

issue

5

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6 February 2018

page(s)

399-401

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6 February 2018

22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Congenital muscular dystrophy: a review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Visual acuity testing of young children with the Cambridge Crowding Cards at 3 and 6 m

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Visual function of prematurely born children with and without perceptual-motor difficulties.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Patterns of visual impairment associated with lesions of the preterm infant brain

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2897%2900222-1

7 January 2021

10.1016/S0887-8994(97)00222-1

Identifiers

DOI

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6 February 2018

1 reference

6 February 2018