Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: genetic testing (Click to remove) Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025 A 53-year-old Woman with Lower Extremity Paresthesias Neurol 94:1105-1108, Dehbashi, S.,et al, 2020 Polycythemia Vera Presenting with Ischemic Strokes in Multiple Arterial Territories Neurol 82:e168-e170, Billakota, S. & Husseini, N.E., 2014 Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing NEJM 370:Doi:10.1056/NEJMoal1401268, Wilson, M.R.,et al, 2014 An unusual cause of stroke and hypoxia BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011 Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia NEJM 362:1326-1333, Case 10-2010, 2010 Alexander Disease, Ventricular Garlands and Abnormalities of the Medulla and Spinal Cord Neurol 66:494-498,468, van der Knaap,M.S.,et al, 2006 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Showing articles 0 to 10 of 10