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Showing articles 0 to 13 of 13 Filter Applied: Kearns-Sayre syndrome (Click to remove) Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Imaging Patterns Characterizing Mitochondrial Leukodystrophies AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021 Myasthenic Symptoms in Patients with Mitochondrial Myopathies Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995 Mitochondrial DNA and Genetic Disease Editorial, Lancet 1:250-2511989., , 1989 Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA Ann Neurol 26:699-708, Hold,I.J.,et al, 1989 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Mitochondrial Myopathies Ann Neurol 17:521-538, DiMauro,S.,et al, 1985 Abrupt Neurological Deterioration in Children With Kearns-Sayre Syndrome Arch Neurol 38:247-250, Coulter,D.L.,et al, 1981 Ophthalmoplegia-Plus Arch Neurol 38:423-426, Okamoto,T.,et al, 1981 Familial Kearns-Sayre syndrome Neurol 29:1172-1174, Schnitzler,E.R.,et al, 1979 Kearns-Sayre Syndrome with Hypoparathyroidism Ann Neurol 3:513, Horwitz,S.J.,et al, 1978 Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Showing articles 0 to 13 of 13