(Q48362804)

11 February 2018

title

Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding concept (English)

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11 February 2018

congenital muscular dystrophy

main subject

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M T Mackay

1

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11 February 2018

A J Kornberg

2

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11 February 2018

L Shield

3

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11 February 2018

E Phelan

4

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11 February 2018

M J Kean

5

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11 February 2018

L T Coleman

6

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11 February 2018

X Dennett

7

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11 February 2018

publication date

1 October 1998

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11 February 2018

Journal of Child Neurology

published in

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11 February 2018

volume

13

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11 February 2018

issue

10

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11 February 2018

page(s)

481-487

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11 February 2018

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Diagnostic criteria for Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Congenital muscular dystrophy with abnormal radiographic myelin pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Occidental type cerebromuscular dystrophy: a report of eleven cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Congenital muscular dystrophy: brain alterations in an unselected series of Western patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Posterior agyria-pachygyria with polymicrogyria: evidence for an inherited neuronal migration disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307389801301003

10.1177/088307389801301003

21 January 2018

Identifiers

DOI

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11 February 2018

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11 February 2018