Cargando…
Serial magnetic resonance imaging findings during severe attacks of familial hemiplegic migraine type 2: a case report
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 responsible for...
Autores principales: | Fear, David, Patel, Misha, Zand, Ramin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8059280/ https://www.ncbi.nlm.nih.gov/pubmed/33882852 http://dx.doi.org/10.1186/s12883-021-02201-z |
Ejemplares similares
-
Intravenous nimodipine worsening prolonged attack of familial hemiplegic migraine
por: Mjåset, Christer, et al.
Publicado: (2008) -
Brain atrophy following hemiplegic migraine attacks
por: Pelzer, Nadine, et al.
Publicado: (2017) -
Familial Hemiplegic Migraine with Severe Attacks: A New Report with ATP1A2 Mutation
por: Martínez, E., et al.
Publicado: (2016) -
Sporadic Hemiplegic Migraine
por: Kana, Tina, et al.
Publicado: (2023) -
Neuropsychologic phenotypes in familial hemiplegic migraine
por: Roccella, Michele
Publicado: (2003)