(Q52538560)

2 May 2018

title

Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome. (English)

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2 May 2018

author name string

Vajsar J

1

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2 May 2018

Ackerley C

2

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2 May 2018

Chitayat D

3

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2 May 2018

Becker LE

4

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2 May 2018

publication date

1 February 2000

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2 May 2018

published in

Pediatric Neurology

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2 May 2018

volume

22

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2 May 2018

issue

2

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2 May 2018

page(s)

139-143

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2 May 2018

Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

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Duchenne dystrophy: Electron microscopic findings pointing to a basic or early abnormality in the plasma membrane of the muscle fiber

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Duchenne muscular dystrophy: plasma membrane loss initiates muscle cell necrosis unless it is repaired

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Sarcolemmal defect and subsarcolemmal lesion in a patient with gamma-sarcoglycan deficiency

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7 January 2021

Muscle pathology and clinical features of the sarcolemmopathies

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7 January 2021

Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy

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7 January 2021

Laminin 2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebroocular dysplasia-muscular dystrophy)

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Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

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Prenatal diagnosis of retinal nonattachment in the Walker‐Warburg syndrome

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Severe classical congenital muscular dystrophy and merosin expression.

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Walker-Warburg syndrome: neurologic features and muscle membrane structure

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Laminin-alpha 2 chain (merosin M) is preserved in the Walker-Warburg syndrome.

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Changes of laminin beta 2 chain expression in congenital muscular dystrophy

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Identifiers

DOI

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2 May 2018

PubMed ID

10738921

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2 May 2018