(Q43542175)

24 November 2017

title

Clinicopathological study on eyes from cases of Fukuyama type congenital muscular dystrophy (English)

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24 November 2017

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Hino N

1

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24 November 2017

Kobayashi M

2

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24 November 2017

Shibata N

3

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24 November 2017

Yamamoto T

4

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24 November 2017

Saito K

5

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24 November 2017

Osawa M

6

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24 November 2017

publication date

1 March 2001

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24 November 2017

published in

Brain and Development

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24 November 2017

volume

23

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24 November 2017

issue

2

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24 November 2017

page(s)

97-107

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Haplotype-phenotype correlation in Fukuyama congenital muscular dystrophy

24 November 2017

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Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome

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Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus

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Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

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Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

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Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

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Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

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24 November 2017

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