Heredodegenerative Disorders, Nervous System
"Heredodegenerative Disorders, Nervous System" 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.
Inherited disorders characterized by progressive atrophy and dysfunction of anatomically or physiologically related neurologic systems.
| Descriptor ID |
D020271
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| MeSH Number(s) |
C10.574.500 C16.320.400
|
| Concept/Terms |
Heredodegenerative Disorders, Nervous System- Heredodegenerative Disorders, Nervous System
- Degenerative Hereditary Diseases, Nervous System
- Degenerative Hereditary Disorders, Nervous System
- Hereditary Diseases, Neurodegenerative
- Disease, Neurodegenerative Hereditary
- Diseases, Neurodegenerative Hereditary
- Hereditary Disease, Neurodegenerative
- Neurodegenerative Hereditary Disease
- Neurodegenerative Hereditary Diseases
- Neurodegenerative Diseases, Hereditary
- Disease, Hereditary Neurodegenerative
- Diseases, Hereditary Neurodegenerative
- Hereditary Neurodegenerative Disease
- Neurodegenerative Disease, Hereditary
- Hereditary-Degenerative Disorders, Nervous System
- Hereditary Degenerative Disorders, Nervous System
- Nervous System Degenerative Hereditary Diseases
- Nervous System Diseases, Degenerative, Hereditary
- Nervous System Hereditary Degenerative Diseases
- Degenerative Disease, Nervous System, Hereditary
- Hereditary Neurodegenerative Diseases
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Below are MeSH descriptors whose meaning is more general than "Heredodegenerative Disorders, Nervous System".
Below are MeSH descriptors whose meaning is more specific than "Heredodegenerative Disorders, Nervous System".
This graph shows the total number of publications written about "Heredodegenerative Disorders, Nervous System" by people in this website by year, and whether "Heredodegenerative Disorders, Nervous System" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2007 | 2 | 0 | 2 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2017 | 1 | 1 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Heredodegenerative Disorders, Nervous System" by people in Profiles.
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MPV17-related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects. Hum Mutat. 2018 04; 39(4):461-470.
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Pleiotropic neuropathological and biochemical alterations associated with Myo5a mutation in a rat Model. Brain Res. 2018 01 15; 1679:155-170.
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Genetic rodent models of brain disorders: Perspectives on experimental approaches and therapeutic strategies. Am J Med Genet C Semin Med Genet. 2017 09; 175(3):368-379.
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PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment. Brain. 2017 Apr 01; 140(4):940-952.
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Genetics and molecular biology of brain calcification. Ageing Res Rev. 2015 Jul; 22:20-38.
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Polyglutamine disease toxicity is regulated by Nemo-like kinase in spinocerebellar ataxia type 1. J Neurosci. 2013 May 29; 33(22):9328-36.
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Astrocytes and disease: a neurodevelopmental perspective. Genes Dev. 2012 May 01; 26(9):891-907.
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Comparative analysis of genetic modifiers in Drosophila points to common and distinct mechanisms of pathogenesis among polyglutamine diseases. Hum Mol Genet. 2008 Feb 01; 17(3):376-90.
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Trinucleotide repeat disorders. Annu Rev Neurosci. 2007; 30:575-621.
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Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation. Alzheimer Dis Assoc Disord. 2007 Jan-Mar; 21(1):1-7.