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Showing articles 0 to 8 of 8 Filter Applied: dementia,familial (Click to remove) Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum Neurol 39:1446-1452, Farlow,M.R.,et al, 1989 Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease BMJ 315:856-857, Fox,N.C.,et al, 1997 Phenotype of Chromosome 14-Linked Familial Alzheimer's Disease in a Large Kindred Ann Neurol 36:368-378, Lampe,T.H.,et al, 1994 Real and Imagined Clinicopathological Limits of"Prior Dementia" Lancet 341:127-129, Brown,P.,et al, 1993 Infectious Prions or Cytotoxic Metabolites? Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993 The Spongiform Encephalopathies, Editorial JNNP 54:761-763, Will,R.G., 1991 Prion Dementia Without Characteristic Pathology Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990 Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis Lancet 2:15-17, Collinge,J.,et al, 1989 Showing articles 0 to 8 of 8