(Q30560481)

24 June 2017

title

MR imaging findings in children with merosin-deficient congenital muscular dystrophy (English)

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congenital muscular dystrophy

24 June 2017

0 references

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Caro PA

1

1 reference

24 June 2017

Scavina M

2

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24 June 2017

Hoffman E

3

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24 June 2017

Pegoraro E

4

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24 June 2017

Marks HG

5

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24 June 2017

publication date

1 February 1999

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American Journal of Neuroradiology

24 June 2017

published in

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24 June 2017

volume

20

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24 June 2017

issue

2

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24 June 2017

page(s)

324-326

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Brain MR in Fukuyama congenital muscular dystrophy.

24 June 2017

cites work

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12 December 2020

Mapping of domains in human laminin using monoclonal antibodies: localization of the neurite-promoting site

1 reference

12 December 2020

Congenital muscular dystrophy of non-Fukuyama type with characteristic CT images

1 reference

12 December 2020

White matter abnormalities in congenital muscular dystrophy

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12 December 2020

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up

1 reference

12 December 2020

Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency

1 reference

12 December 2020

Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency

1 reference

12 December 2020

Congenital muscle disease and abnormal findings on computerized tomography.

1 reference

12 December 2020

Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Localization of merosin in the normal human brain: implications for congenital muscular dystrophy with merosin deficiency

1 reference

12 December 2020

Congenital muscular dystrophy with merosin deficiency

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

Merosin promotes cell attachment and neurite outgrowth and is a component of the neurite-promoting factor of RN22 schwannoma cells

1 reference

12 December 2020

Identifiers

1 reference