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Showing articles 0 to 6 of 6 Filter Applied: hearing loss (Click to remove) Cogan Syndrome An Analysis of Reported Neurological Manifestations The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012 Neurofibromatosis Type 2 Lancet 373:1974-1986, Astagiri,A.R.,et al, 2009 Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998 Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Showing articles 0 to 6 of 6