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Showing articles 0 to 9 of 9 Filter Applied: gene mutation (Click to remove) Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients Medicine 86:1-7, Cottin,V.,et al, 2007 Metabolic Disease and Stroke: MELAS emedicine.com, Mandava,P.,et al, 2006 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Pes Cavus and Neuropathy Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019 A Child with Arthrogryposis Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018 Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man Neurol 88:e26-e29, Qin, C.,et al, 2017 A Neonate with Micrognathia and Hypotonia Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016 Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Showing articles 0 to 9 of 9