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Showing articles 0 to 8 of 8 Filter Applied: molecular genetics (Click to remove) Pediatric Leigh Syndrome Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020 Unusual Variants of Alexander's Disease Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Fragile X Premutation With Atypical Symptoms at Onset Arch Neurol 63:1135-1138, Cellini,E.,et al, 2006 Primary Anaplastic Large Cell Lymphoma of the Central Nervous System Am J Surg Pathol 27:487-493, George, D.H.,et al, 2003 von Hippel-Lindau Disease Medicine 76:381-391, Maher,E.R.&Kaelin,W.G., 1997 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Canavan Disease:From Spongy Degeneration to Molecular Analysis J Pediatr 127:511-517, Matalon,R.,et al, 1995 Showing articles 0 to 8 of 8