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Journal 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 LarnerDiagnostics (Basel, Switzerland)|November 10, 2019
Diagnosis of Dementia and Cognitive ImpairmentAndrew J LarnerPostgraduate Medicine|March 6, 2020
The 'attended alone' and 'attended with' signs in the assessment of cognitive impairment: a revalidationA J LarnerNeurodegenerative Disease Management|September 19, 2018
Mini-Mental State Examination: diagnostic test accuracy study in primary care referralsAndrew J LarnerJournal of Geriatric Psychiatry and Neurology|March 15, 2015
AD8 Informant Questionnaire for Cognitive Impairment: Pragmatic Diagnostic Test Accuracy StudyA J LarnerPageof 34