"Migraine with Aura" 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 subtype of migraine disorder, characterized by recurrent attacks of reversible neurological symptoms (aura) that precede or accompany the headache. Aura may include a combination of sensory disturbances, such as blurred VISION; HALLUCINATIONS; VERTIGO; NUMBNESS; and difficulty in concentrating and speaking. Aura is usually followed by features of the COMMON MIGRAINE, such as PHOTOPHOBIA; PHONOPHOBIA; and NAUSEA. (International Classification of Headache Disorders, 2nd ed. Cephalalgia 2004: suppl 1)
| Descriptor ID |
D020325
|
| MeSH Number(s) |
C10.228.140.546.399.750.250
|
| Concept/Terms |
Familial Hemiplegic Migraine- Familial Hemiplegic Migraine
- Familial Hemiplegic Migraines
- Hemiplegic-Ophthalmoplegic Migraine
- Hemiplegic Migraine, Familial
Migraine with Prolonged Aura- Migraine with Prolonged Aura
- Migraine, Prolonged Aura
- Prolonged Aura Migraine
- Complicated Migraine
- Migraine, Complicated
Basilar-Type Migraine- Basilar-Type Migraine
- Basilar Type Migraine
- Migraine, Basilar-Type
- Basilar Migraine
- Basilar Migraines
- Migraine, Basilar
- Basilar Artery Migraine
- Migraine, Basilar Artery
|
Below are MeSH descriptors whose meaning is more general than "Migraine with Aura".
Below are MeSH descriptors whose meaning is more specific than "Migraine with Aura".
This graph shows the total number of publications written about "Migraine with Aura" by people in this website by year, and whether "Migraine with Aura" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 1 | 0 | 1 |
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Below are the most recent publications written about "Migraine with Aura" by people in Profiles.
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Genetic association studies of the chromosome 15 GABA-A receptor cluster in migraine with aura. Am J Med Genet B Neuropsychiatr Genet. 2008 Jan 05; 147B(1):37-41.
MeSH information
