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Nature|July 3, 1999
A stop-codon mutation in the BRI gene associated with familial British dementiaR Vidal, B Frangione, A Rostagno, et al.Annals of the New York Academy of Sciences|May 20, 2000
A newly formed amyloidogenic fragment due to a stop codon mutation causes familial British dementiaJ Ghiso, R Vidal, A Rostagno, et al.Annals of the New York Academy of Sciences|February 24, 2001
Amyloidogenesis in familial British dementia is associated with a genetic defect on chromosome 13J Ghiso, R Vidal, A Rostagno, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1983
Focal paroxysmal kinesigenic choreoathetosisG PlantBritish Journal of Audiology|February 1, 1984
The effects of an acquired profound hearing loss on speech production. A case studyG PlantEar and Hearing|October 31, 1998
Training in the use of a tactile supplement to lipreading: a long-term case studyG PlantEuropean Journal of Disorders of Communication : the Journal of the College of Speech and Language Therapists, London|January 1, 1993
The speech of adults with acquired profound hearing losses. I: A perceptual evaluationG PlantBrain : a Journal of Neurology|April 25, 2000
Familial British dementia with amyloid angiopathy: early clinical, neuropsychological and imaging findingsS Mead, M James-Galton, T Revesz, et al.Rheumatology (Oxford, England)|December 22, 2005
The prevalence of headache in Behçet's syndromeD KiddPageof 62