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Showing articles 0 to 8 of 8 Filter Applied: neuronal ceroid-lipofuscinosis (Click to remove) Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis NEJM 364:1062-1074, Case 8-2011, 2011 A 23-Year-Old Man With Seizures and Visual Deficit Neurol 70:73-78, Boustany,R.-M.,et al, 2008 CT in Ceroid Lipofuscinosis Neurol 37:1025-1026, Dunn,D.W., 1987 Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy Neurol 90:e1827-e1831, Xiao, F.,et al, 2018 Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease) Adams & Victors Principles of Neurology, Chp 37, pg 973, Ropper, A.H.,et al, 2014 Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects Lancet Neurol 4:239-248, Shahwan, A., et al, 2005 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978 Showing articles 0 to 8 of 8