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Showing articles 0 to 3 of 3 Filter Applied: genetic testing (Click to remove) The Phenotypic Continuum of ATP1A3-Related Disorders Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing NEJM 370:Doi:10.1056/NEJMoal1401268, Wilson, M.R.,et al, 2014 Showing articles 0 to 3 of 3