Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report
Abstract Background Hemiplegic migraines represent a heterogeneous disorder with various presentations. Hemiplegic migraines are classified as sporadic or familial based on the presence of family history, but both subtypes have an underlying genetic etiology. Mutations in the ATP1A2 gene are respons...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2021-04-01
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| Sarja: | BMC Neurology |
| Aiheet: | |
| Linkit: | https://doi.org/10.1186/s12883-021-02201-z |
| Tagit: |
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