Brain abnormalities in Duchenne muscular dystrophy: phosphorus-31 magnetic resonance spectroscopy and neuropsychological study. (Q52016269)

19 April 2018

title

Brain abnormalities in Duchenne muscular dystrophy: phosphorus-31 magnetic resonance spectroscopy and neuropsychological study. (English)

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19 April 2018

Duchenne muscular dystrophy

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8

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author name string

I Tracey

1

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19 April 2018

R B Scott

2

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C H Thompson

3

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19 April 2018

J F Dunn

4

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19 April 2018

P R Barnes

5

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P Styles

6

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19 April 2018

G J Kemp

7

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19 April 2018

M Pike

9

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19 April 2018

G K Radda

10

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language of work or name

English

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publication date

1 May 1995

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19 April 2018

published in

The Lancet

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19 April 2018

volume

345

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19 April 2018

issue

8960

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19 April 2018

page(s)

1260-1264

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19 April 2018

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental ability

cites work

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Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

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Expression of the murine Duchenne muscular dystrophy gene in muscle and brain

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The emerging family of dystrophin-related proteins.

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Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons.

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Detection of dystrophin in the postsynaptic density of rat brain and deficiency in a mouse model of Duchenne muscular dystrophy

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Cell and fiber type distribution of dystrophin

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Central nervous system involvement in progressive muscular dystrophy

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The central nervous system in Duchenne muscular dystrophy

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The cerebral defect and myopathy in Duchenne muscular dystrophy A comparative clinicopathological study

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Brain morphology in Duchenne muscular dystrophy: a Golgi study

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A 31P-NMR study of muscle exercise metabolism in mdx mice: evidence for abnormal pH regulation

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Passive avoidance behaviour deficit in the mdx mouse

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Energy status of cells lacking dystrophin: an in vivo/in vitro study of mdx mouse skeletal muscle

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Cellular energetics of dystrophic muscle

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Flat crossed-coil detector for blood flow measurement using nuclear magnetic resonance

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Etiology of intellectual impairment in Duchenne muscular dystrophy

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Defective brain energy metabolism shown by in vivo 31P MR spectroscopy in 28 patients with mitochondrial cytopathies

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Total ion content of skeletal and cardiac muscle in the mdx mouse dystrophy: Ca2+ is elevated at all ages

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Sodium is elevated in mdx muscles: ionic interactions in dystrophic cells

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7 January 2021

Exercise metabolism in Duchenne muscular dystrophy: a biochemical and [31P]-nuclear magnetic resonance study of mdx mice

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7 January 2021

Regulation of intracellular free calcium in normal and dystrophic mouse cerebellar neurons

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7 January 2021

10.1016/S0140-6736(95)90923-0

Identifiers

DOI

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19 April 2018

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19 April 2018