"Peripheral Nervous System Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves.
Descriptor ID |
D010523
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MeSH Number(s) |
C10.668.829
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Concept/Terms |
Peripheral Nervous System Diseases- Peripheral Nervous System Diseases
- Peripheral Nervous System Disease
- PNS Diseases
- PNS Disease
- Peripheral Neuropathies
- Neuropathy, Peripheral
- Peripheral Neuropathy
- PNS (Peripheral Nervous System) Diseases
- Peripheral Nerve Diseases
- Nerve Disease, Peripheral
- Nerve Diseases, Peripheral
- Peripheral Nerve Disease
- Peripheral Nervous System Disorders
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Below are MeSH descriptors whose meaning is more general than "Peripheral Nervous System Diseases".
Below are MeSH descriptors whose meaning is more specific than "Peripheral Nervous System Diseases".
This graph shows the total number of publications written about "Peripheral Nervous System Diseases" by people in this website by year, and whether "Peripheral Nervous System Diseases" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2002 | 1 | 0 | 1 |
2007 | 1 | 0 | 1 |
2012 | 2 | 0 | 2 |
2014 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 0 | 1 | 1 |
2021 | 1 | 0 | 1 |
2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Peripheral Nervous System Diseases" by people in Profiles.
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Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L-Associated Neuropathy. Genes (Basel). 2022 12 14; 13(12).
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Recurrent abdominal pain in hereditary sensory autonomic neuropathy type II (HSAN-II). Rev Neurol (Paris). 2021 Dec; 177(10):1307-1309.
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General and Abdominal Obesity and Incident Distal Sensorimotor Polyneuropathy: Insights Into Inflammatory Biomarkers as Potential Mediators in the KORA F4/FF4 Cohort. Diabetes Care. 2019 02; 42(2):240-247.
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Peripheral nerve atrophy together with higher cerebrospinal fluid progranulin indicate axonal damage in amyotrophic lateral sclerosis. Muscle Nerve. 2018 02; 57(2):273-278.
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Differential association between biomarkers of subclinical inflammation and painful polyneuropathy: results from the KORA F4 study. Diabetes Care. 2015 Jan; 38(1):91-6.
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Older subjects with diabetes and prediabetes are frequently unaware of having distal sensorimotor polyneuropathy: the KORA F4 study. Diabetes Care. 2013 May; 36(5):1141-6.
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Exome sequencing identifies a REEP1 mutation involved in distal hereditary motor neuropathy type V. Am J Hum Genet. 2012 Jul 13; 91(1):139-45.
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Phenotypic characterization of hypomyelination and congenital cataract. Ann Neurol. 2007 Aug; 62(2):121-7.
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A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. J Child Neurol. 2002 Mar; 17(3):233-6.