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Psychiatry Research|March 27, 1995
The Cambridge Neurological Inventory: a clinical instrument for assessment of soft neurological signs in psychiatric patientsE Y Chen, J Shapleske, R Luque, et al.Brain : a Journal of Neurology|December 3, 1999
Huntington's disease progression. PET and clinical observationsT C Andrews, R A Weeks, N Turjanski, et al.Journal of Neurology|June 5, 2016
Cognition and eating behavior in amyotrophic lateral sclerosis: effect on survivalR M Ahmed, J Caga, E Devenney, et al.Neurology|December 25, 2003
Profile of cognitive progression in early Huntington's diseaseA K Ho, B J Sahakian, R G Brown, et al.Neuropsychologia|April 9, 1998
Face processing impairments after encephalitis: amygdala damage and recognition of fearP Broks, A W Young, E J Maratos, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 19, 2004
Similar early clinical presentations in familial and non-familial frontotemporal dementiaO Piguet, W S Brooks, G M Halliday, et al.Psychiatry Research|July 7, 2001
Psychiatric symptoms and CAG repeats in neurologically asymptomatic Huntington's disease gene carriersG E Berrios, A C Wagle, I S Marková, et al.Brain Communications|August 1, 2022
Utility of the Addenbrooke's Cognitive Examination III online calculator to differentiate the primary progressive aphasia variantsD Foxe, A Hu, S C Cheung, et al.Journal of the American Society for Mass Spectrometry|September 29, 2022
Next-Generation Infrared Matrix-Assisted Laser Desorption Electrospray Ionization Source for Mass Spectrometry Imaging and High-Throughput ScreeningKevan T Knizner, Jacob P Guymon, Kenneth P Garrard, et al.Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.Pageof 27