"Cerebellar Vermis" 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.
A subregion of the CEREBELLAR CORTEX, located along the midsagittal plane of the CEREBELLUM.
| Descriptor ID |
D065814
|
| MeSH Number(s) |
A08.186.211.132.810.428.200.212.299
|
| Concept/Terms |
Uvula of Cerebellum- Uvula of Cerebellum
- Cerebellum Uvula
- Cerebellum Uvulas
- Lobule IX
- Lobule IXs
- Lobule 9
- Lobule 9s
|
Below are MeSH descriptors whose meaning is more general than "Cerebellar Vermis".
Below are MeSH descriptors whose meaning is more specific than "Cerebellar Vermis".
This graph shows the total number of publications written about "Cerebellar Vermis" by people in this website by year, and whether "Cerebellar Vermis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 0 | 1 | 1 |
| 2020 | 0 | 2 | 2 |
| 2023 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cerebellar Vermis" by people in Profiles.
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Novel association of Dandy-Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome. Am J Med Genet A. 2023 11; 191(11):2757-2767.
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Defining the phenotypical spectrum associated with variants in TUBB2A. J Med Genet. 2021 01; 58(1):33-40.
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MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes. Hum Mol Genet. 2015 Sep 15; 24(18):5313-25.