High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy (Q41739332)

8 October 2017

title

High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophy (English)

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magnetic resonance imaging of the brain

8 October 2017

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Dubowitz DJ

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8 October 2017

Tyszka JM

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8 October 2017

Sewry CA

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8 October 2017

Moats RA

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8 October 2017

Scadeng M

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8 October 2017

Dubowitz V

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8 October 2017

publication date

1 June 2000

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8 October 2017

published in

Neuromuscular Disorders

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8 October 2017

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8 October 2017

issue

4-5

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8 October 2017

page(s)

292-298

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

8 October 2017

cites work

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PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy

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Parameter relations for the Shinnar-Le Roux selective excitation pulse design algorithm [NMR imaging].

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

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7 January 2021

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7 January 2021

Expression of laminin alpha1, alpha2, alpha4, and alpha5 chains, fibronectin, and tenascin-C in skeletal muscle of dystrophic 129ReJ dy/dy mice

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7 January 2021

Laminins of the adult mammalian CNS; laminin-α2 (merosin M-) chain immunoreactivity is associated with neuronal processes

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Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

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7 January 2021

10.1016/S0960-8966(00)00104-8

Identifiers

DOI

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8 October 2017

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