Cited by 21Amyotrophic Lateral Sclerosis ResearchMitochondrial Function and PathologyHereditary Neurological Disorders

Ultrastructural Mitochondrial Abnormalities in Patients With Sporadic Amyotrophic Lateral Sclerosis

Napoli, Laura·2011·Archives of Neurology

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Crossref · 10.1001/archneur.68.12.1612

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6 of 6 references verified0 citation errors · 0 not checkable

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  • Accumulations of dysmorphic and enlarged mitochondria, many with deficiencies of critical oxidative enzymes, in anterior horn cells, intramuscular nerves, and skeletal muscle are characteristic of sALS.

    “Accumulations of dysmorphic and enlarged mitochondria, many with deficiencies of critical oxidative enzymes, in anterior horn cells, intramuscular nerves, and skeletal muscle are characteristic of sALS [281–285].”

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Authors
Napoli, L.
Affiliations
University of Milan (IT)
Corresponding author
Napoli, Laura
Venue
Archives of Neurology
Published
2011-12-01
Volume
68
Issue
12
Pages
1612
ISSN
0003-9942 (ISSN-L)
OpenAlex
W2089322876
Cited by
21
References
6
Citations by year
2026: 3 · 2024: 2 · 2023: 3 · 2022: 5 · 2021: 2 · 2020: 2 · 2019: 1 · 2018: 1 · 2013: 1 · 2012: 1
FWCI
0.41
Type
journal article
Language
en
Open access
closed
Locations
  • Archives of Neurology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
Keywords
amyotrophic lateral sclerosis, sporadic ALS, mitochondrial abnormalities, mitochondrial ultrastructure, motor neuron disease
MeSH terms
Amyotrophic Lateral Sclerosis, Humans, Microscopy, Electron, Mitochondria

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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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