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Showing articles 0 to 13 of 13 Filter Applied: deafness (Click to remove) Reversible Cerebellocerebral Disorder in Primary Hemochromatosis Arch Neurol 34:123, Singh,N.,et al, 1977 Chronic Meningitis Medicine 55:341, Ellner,J.J.,et al, 1976 Central Nervous System Manifestations of Periarteritis Nodosa Neurol 15:114, Ford,R.G.,et al, 1965 Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 Cogan Syndrome www.medlink.com, Feb, Ramachandran, T.S., 2010 Retinocochleocerebral Vasculopathy Medicine 77:12-40, Petty,G.W.,et al, 1998 Clinicopath Conf Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995 Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women Stroke 23:903-907, Schwitter,J.,et al, 1992 Neurological Complications of Infantile Osteopetrosis Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977 Mollaret's Meningitis & Differential Diagnosis of Recurrent Meningitis Am J Med 52:128, Hermans,P.,et al, 1972 The Mucopolysaccharidoses (Ed) , 4th Edition, the C. V. Mosby Co, 1971, Chp. 11, p. p. 521-686., McKusick,V.A., 1971 Hunter's Syndrome, In Recognizable Patterns Of Human Malformation, Genetic, Embryologic, & Clinical Aspects, by Smith W. B. , Saunders Co. , 1970, 248-249., David,W., 1970 Showing articles 0 to 13 of 13