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Showing articles 0 to 8 of 8 Filter Applied: familial (Click to remove) Paroxysmal Extreme Pain Disorder (Previously Familial Rectal Pain Syndrome) Neurol 69:586-595, Fertleman,C.R.,et al, 2007 Variable Presentation of Brugada Syndrome: Lessons from Three Generations with Syncope BMJ 326:1078-1079, Plunkett,A.,et al, 2003 Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996 Familial Occurrence of Neurocardiogenic Syncope NEJM 331:205, Cooper,C.J.,et al, 1994 Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families Ann Neurol 41:150-159, Heutnik,P.,et al, 1997 Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia Ann Neurol 39:166-173, Turner,R.S.,et al, 1996 Progressive Language Disorder Due to Lobar Atrophy Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992 Clinicopath Conf Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992 Showing articles 0 to 8 of 8