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Showing articles 0 to 15 of 15 Filter Applied: molecular genetics (Click to remove) A Variegated Squirrel Bornavirus Associated with Fatal Human Encephalitis NEJM 373:154-162, Hoffmann, B.,et al, 2015 Actionable Diagnosis of Neuroleptospirosis by Next-Generation Sequencing NEJM 370:Doi:10.1056/NEJMoal1401268, Wilson, M.R.,et al, 2014 The Autosomal Recessive Cerebellar Ataxias NEJM 366:636-646, Anheim,M.,et al, 2012 Whipples Disease NEJM 356:55-66, Fenollar,F.,et al, 2007 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,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 CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes Neurol 58:390-396,339, Gleissner,B.,et al, 2002 Sickle Cell Disease: The Neurological Complications Ann Neurol 51:543-552, Prengler,M.,et al, 2002 A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review The Neurologist 8:302-312, Thambisetty,M.,et al, 2002 The Muscular Dystrophies BMJ 317:991-995, Emery,A.E.H., 1998 Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan) Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation Lancet 338:1562-1563, , 1991 Showing articles 0 to 15 of 15