THE MYELONEUROPATHY VARIANT OF ADRENOLEUKODYSTROPHY: 26
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In AMN patients, the fasciculus gracilis shows a prominent loss of myelinated fibers and oligodendrocytes, associated with axonal atrophy and very thin or disintegrating myelin sheaths.
“In AMN patients, the fasciculus gracilis shows a prominent loss of myelinated fibers and OLs [18], associated with axonal atrophy and very thin or disintegrating myelin sheaths [49,82].”
From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [18]
Peripheral nerves in AMN show variable and mild lesions of chronic axonal atrophy with secondary demyelination.
“The few studies on peripheral nerves in AMN [16,18,20,82,84,85,86] highlight variable and mild lesions of chronic axonal atrophy with secondary demyelination [49].”
From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [18]
Cited by
Sorted by citations
Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy
Powers, J. M., DeCiero, D. P., Ito, M., Moser, A. B., & Moser, H. W. (2000) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/59.2.89 · Cited by 204 · see citing works
Self-citationRevisiting the Pathogenesis of X-Linked Adrenoleukodystrophy
Bougnères, P., & Le Stunff, C. (2025) · Genes · doi:10.3390/genes16050590 · Cited by 11 · see citing works
- Authors
- Schaumburq, H. H., Powers, J. M., Spencer, P. S., Raine, C. S., Prineas, J. W., & Boehme, D. M.
- Venue
- Journal of Neuropathology and Experimental Neurology
- Publisher
- Oxford University Press (OUP)
- Published
- 1976-05
- Volume
- 35
- Issue
- 3
- Pages
- 312
- ISSN
- 0022-3069 (ISSN-L)
- OpenAlex
- W1976415157
- Cited by
- 7
- References
- 0
- Citations by year
- 2025: 2 · 2024: 1 · 2022: 1
- FWCI
- 0.00
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neuropathology & Experimental Neurology (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
- Keywords
- adrenoleukodystrophy, myeloneuropathy, leukodystrophy, myelin pathology
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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