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Showing articles 0 to 12 of 12 Filter Applied: intellectual deficit (Click to remove) A 54-year-old woman with Dementia, Myoclonus, and Ataxia Neurol 89:e7-e12, Ali, F.,et al, 2017 Sarcoidosis Limbic Encephalitis Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017 Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis UptoDate Oct. 2014, McClain, K.L., 2014 Neurofibromatosis Type I in Children J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990 Two Cases of Van Buchem's Disease JNNP 45:913-918, Dixon,J.M.,et al, 1982 Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters Am J Med 69:64-74, Whythe,M.P.,et al, 1980 Diagnostic Exome, Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability NEJM 367:1921-1929, Ligt, J.,et al, 2012 Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population JAMA 291:460-469, Jacquemont,S.,et al, 2004 Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy Neurol 46:461-465, North,K.N.,et al, 1996 Diagnostic Guidelines in Central Nervous System Whipple's Disease Ann Neurol 40:561-568, Louis,E.D.,et al, 1996 Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992 Showing articles 0 to 12 of 12