(Q33882324)

29 July 2017

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title

Adrenomyeloneuropathy: a neuropathologic review featuring its noninflammatory myelopathy (English)

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29 July 2017

Powers JM

1

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29 July 2017

DeCiero DP

2

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29 July 2017

Ito M

3

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29 July 2017

Moser AB

4

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29 July 2017

Moser HW

5

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29 July 2017

publication date

1 February 2000

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Journal of Neuropathology & Experimental Neurology

29 July 2017

published in

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29 July 2017

volume

59

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29 July 2017

issue

2

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29 July 2017

page(s)

89-102

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Spastic paraplegia associated with Addison's disease: adult variant of adreno-leukodystrophy

29 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy

21 January 2018

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Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Localized proton magnetic resonance spectroscopy in patients with adult adrenoleukodystrophy. Increase of choline compounds in normal appearing white matter

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oil

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Mutational analysis and genotype-phenotype correlation of 29 unrelated Japanese patients with X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

X-linked adrenoleukodystrophy: genes, mutations, and phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Adrenoleukodystrophy: phenotypic variability and implications for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil"

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Effects of long-chain, saturated fatty acids on membrane microviscosity and adrenocorticotropin responsiveness of human adrenocortical cells in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Axonal transection in the lesions of multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Pathological study of corticospinal-tract degeneration in Friedreich's ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

The sensory neuropathy of Friedreich's ataxia: an autopsy study of a case with prolonged survival

21 January 2018

1 reference

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The peripheral sensory pathway in friedreich's ataxia. An examination by light and electron microscopy of the posterior nerve roots, posterior root ganglia, and peripheral sensory nerves in cases of friedreich's ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

The yeast connection to Friedreich ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Does a defect of energy metabolism in the nerve fiber underlie axonal degeneration in polyneuropathies?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Hereditary ataxia with sensory neuronopathy: Biemond's ataxia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Pathology of peroneal muscular atrophy (Charcot-Marie-Tooth disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Hereditary motor and sensory neuropathy type II. Clinicopathological study of a family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Macrophage responses and myelin clearance during Wallerian degeneration: relevance to immune-mediated demyelination

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Fatty acid abnormality in adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Membrane microviscosity is increased in the erythrocytes of patients with adrenoleukodystrophy and adrenomyeloneuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Brain gangliosides in adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Interactions of a very long chain fatty acid with model membranes and serum albumin. Implications for the pathogenesis of adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

The distribution of ganglioside-like moieties in peripheral nerves

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

Mice lacking complex gangliosides develop Wallerian degeneration and myelination defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

A mouse model for X-linked adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.2.89

21 January 2018

Identifiers

DOI

10.1093/JNEN/59.2.89

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29 July 2017

1 reference