Research graph
References from Acute neuro-inflammatory presentation of ATP1A3 variants: Case reports of three patients with different phenotypes. Local targets link to admitted publications; unresolved targets remain external evidence.
Distinct neurological disorders with ATP1A3 mutations
10.1016/s1474-4422(14)70011-0 · 2014 · External reference
Alternating hemiplegia of childhood: clinical manifestations and long-term outcome
10.1016/s0887-8994(00)00157-0 · 2000 · External reference
Fever-induced paroxysmal weakness and encephalopathy, a new phenotype of ATP1A3 mutation
10.1016/j.pediatrneurol.2017.04.022 · 2017 · External reference
ATP1A3-Related disorders: an ever-expanding clinical spectrum
10.3389/fneur.2021.637890 · 2021 · External reference
Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient
10.1212/nxi.0000000000000663 · 2020 · External reference
Pediatric auto-immune encephalitis
2021 · External reference
Variants of ATP1A3 in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)-report of two cases and literature review
10.1002/mgg3.1772 · 2021 · External reference
De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis
10.1186/s12883-016-0680-6 · 2016 · External reference
Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation
10.1111/dmcn.12927 · 2015 · External reference
Chinese patients with p.Arg756 mutations of ATP1A3: clinical manifestations, treatment, and follow-up
10.1002/ped4.12310 · 2022 · External reference
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism
10.1016/j.neuron.2004.06.028 · 2004 · External reference
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
10.1038/ng.2358 · 2012 · External reference
Management of alternating hemiplegia of childhood: a review
10.1016/j.pediatrneurol.2019.10.003 · 2020 · External reference
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism
10.1212/wnl.0000000000000473 · 2014 · External reference
Molecular and clinical characteristics of ATP1A3-related diseases
2022 · External reference
ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood–potential target of treatment?
10.1016/j.braindev.2015.01.003 · 2015 · External reference
Variants of ATP1A3 in residue 756 cause a separate phenotype of relapsing encephalopathy with cerebellar ataxia (RECA)-report of two cases and literature review
10.1002/mgg3.1772 · ExternalCitation · doi-reference
Chinese patients with p.Arg756 mutations of ATP1A3: clinical manifestations, treatment, and follow-up
10.1002/ped4.12310 · ExternalCitation · doi-reference
ATP1A3 mutation in a Chinese girl with alternating hemiplegia of childhood–potential target of treatment?
10.1016/j.braindev.2015.01.003 · ExternalCitation · doi-reference
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism
10.1016/j.neuron.2004.06.028 · ExternalCitation · doi-reference
Fever-induced paroxysmal weakness and encephalopathy, a new phenotype of ATP1A3 mutation
10.1016/j.pediatrneurol.2017.04.022 · ExternalCitation · doi-reference
Management of alternating hemiplegia of childhood: a review
10.1016/j.pediatrneurol.2019.10.003 · ExternalCitation · doi-reference
Alternating hemiplegia of childhood: clinical manifestations and long-term outcome
10.1016/s0887-8994(00)00157-0 · ExternalCitation · doi-reference
Distinct neurological disorders with ATP1A3 mutations
10.1016/s1474-4422(14)70011-0 · ExternalCitation · doi-reference
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood
10.1038/ng.2358 · ExternalCitation · doi-reference
Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation
10.1111/dmcn.12927 · ExternalCitation · doi-reference
De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis
10.1186/s12883-016-0680-6 · ExternalCitation · doi-reference
Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient
10.1212/nxi.0000000000000663 · ExternalCitation · doi-reference
Paroxysmal features responding to flunarizine in a child with rapid-onset dystonia-parkinsonism
10.1212/wnl.0000000000000473 · ExternalCitation · doi-reference
ATP1A3-Related disorders: an ever-expanding clinical spectrum
10.3389/fneur.2021.637890 · ExternalCitation · doi-reference
