 Malformations of Cortical Development, Group I
"Malformations of Cortical Development, Group I" 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.
Cortical malformations secondary to abnormal neuronal and glial CELL PROLIFERATION or APOPTOSIS in NEUROGENESIS. This group includes congenital MICROCEPHALIES; MICROLISSENCEPHALIES, megalencephalies, HEMIMEGALENCEPHALIES and cortical dysplasias with balloon cells.
| Descriptor ID |
D065703
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| MeSH Number(s) |
C10.500.507.400 C16.131.666.507.400
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| Concept/Terms |
Malformations of Cortical Development, Group I- Malformations of Cortical Development, Group I
- Malformations Due to Abnormal Neuronal and Glial Proliferation or Apoptosis
- Malformations Secondary to Abnormal Neuronal and Glial Proliferation or Apoptosis
- Abnormal Proliferation Cortical Malformations
- Cortical Malformations, Group I
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Below are MeSH descriptors whose meaning is more general than "Malformations of Cortical Development, Group I".
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This graph shows the total number of publications written about "Malformations of Cortical Development, Group I" by people in this website by year, and whether "Malformations of Cortical Development, Group I" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Malformations of Cortical Development, Group I" by people in Profiles.
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Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, Von Allmen GK, Rodziyevska O, Bhattacharjee MB, Lidov HGW, Vogel H, Grant GA, Porter BE, Poduri AH, Crino PB, Heinzen EL. Somatic variants in diverse genes leads to a spectrum of focal cortical malformations. Brain. 2022 08 27; 145(8):2704-2720.
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