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Early Treatment in Acute Severe Encephalopathy Caused by ATP1A2 Mutation of Familial Hemiplegic Migraine Type 2: Case Report and Literature Review.
Du Y, Li C, Duan FJ, Zhao C, Zhang W. Du Y, et al. Neuropediatrics. 2020 Jun;51(3):215-220. doi: 10.1055/s-0039-3400986. Epub 2019 Nov 25. Neuropediatrics. 2020. PMID: 31766058 Review.
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant inheritance disorder caused by ATP1A2 mutation, and the clinical spectrum is heterogeneous even with acute severe encephalopathy. ...
Familial hemiplegic migraine type 2 (FHM2) is an autosomal dominant inheritance disorder caused by ATP1A2 …
Zebrafish as a novel model to assess Na+/K(+)-ATPase-related neurological disorders.
Doğanli C, Oxvig C, Lykke-Hartmann K. Doğanli C, et al. Neurosci Biobehav Rev. 2013 Dec;37(10 Pt 2):2774-87. doi: 10.1016/j.neubiorev.2013.09.013. Epub 2013 Oct 1. Neurosci Biobehav Rev. 2013. PMID: 24091024 Review.
Na(+)/K(+)-ATPase mutations are associated with neurological disorders, where mutations in the Na(+)/K(+)-ATPase alpha2 and alpha3 isoforms cause Familial hemiplegic migraine type 2 (FHM2) and Rapid-onset dystonia-parkinsonism (RDP)/Alternating …
Na(+)/K(+)-ATPase mutations are associated with neurological disorders, where mutations in the Na(+)/K(+)-ATPase alpha2 and alpha3 isoforms …