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Showing articles 0 to 8 of 8 Filter Applied: genetic testing (Click to remove) Neonatal Seizures NEJM 388:1692-1700, Ropper.A.H., 2023 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 Congenital Myasthenic Syndromes in Adult Neurology Clinic Neurol 91:e1770-e1777, Kao, J.C.,et al, 2018 A Child with Delayed Motor Milestones and Ptosis Neurol 88:e158-e163, Ghosh, P.S., 2017 Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society Neurol 73:887-897, Ashwal,S.,et al, 2009 New Strategy for Prenatal Diagnosis of X-Linked Disorders NEJM 346:1502, Costa,J.,et al, 2002 The Polymerase Chain Reaction:Application to Nervous System Disease Ann Neurol 34:513-523, Darnell,R.B., 1993 Showing articles 0 to 8 of 8