 Migraine with Aura
"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
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| MeSH Number(s) |
C10.228.140.546.399.750.250
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| Concept/Terms |
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
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2003 | 1 | 0 | 1 | | 2019 | 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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Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan; 63(1):103624.
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Swoboda KJ, Kanavakis E, Xaidara A, Johnson JE, Leppert MF, Schlesinger-Massart MB, Ptacek LJ, Silver K, Youroukos S. Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. Ann Neurol. 2004 Jun; 55(6):884-7.
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Kunkler PE, Kraig RP. Hippocampal spreading depression bilaterally activates the caudal trigeminal nucleus in rodents. Hippocampus. 2003; 13(7):835-44.
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