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International Journal of Clinical Practice|March 17, 2007
Monogenic Mendelian disorders in general neurological practiceA J LarnerJournal of the Neurological Sciences|September 22, 2009
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutationA J LarnerThe British Journal of Clinical Practice|November 1, 1995
Normalisation of slow-relaxing tendon reflexes (Woltman's sign) after cardiac pacing for complete heart blockA J LarnerJournal of Geriatric Psychiatry and Neurology|December 27, 2016
Short Montreal Cognitive AssessmentA J LarnerJournal of Alzheimer'S Disease : JAD|August 17, 2013
Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationshipsA J LarnerPostgraduate Medicine|March 6, 2020
The 'attended alone' and 'attended with' signs in the assessment of cognitive impairment: a revalidationA J LarnerJournal of Geriatric Psychiatry and Neurology|March 15, 2015
AD8 Informant Questionnaire for Cognitive Impairment: Pragmatic Diagnostic Test Accuracy StudyA J LarnerPageof 13