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Showing articles 0 to 3 of 3 Filter Applied: paroxysmal neurologic deficits (Click to remove) The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012 Slater Revisited:6 Year Follow Up Study of Pts with Medically Unexplained Motor Symptoms BMJ 316:582-586, 5641998., Crimlisk,H.L.,et al, 1998 Showing articles 0 to 3 of 3