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Genome Medicine|February 1, 2020
A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing dataRamakrishnan Rajagopalan, Jill R Murrell, Minjie Luo, et al.Journal of Alzheimer'S Disease : JAD|August 18, 2006
Mutations in the tau gene (MAPT) in FTDP-17: the family with Multiple System Tauopathy with Presenile Dementia (MSTD)Maria Grazia Spillantini, Jill R Murrell, Michel Goedert, et al.Journal of Neuropathology and Experimental Neurology|October 6, 2007
Corticobasal syndrome associated with the A9D Progranulin mutationSalvatore Spina, Jill R Murrell, Edward D Huey, et al.Journal of Neuropathology and Experimental Neurology|June 6, 2019
Diffuse Lewy Body Disease and Alzheimer Disease: Neuropathologic Phenotype Associated With the PSEN1 p.A396T MutationDibson D Gondim, Adrian Oblak, Jill R Murrell, et al.Journal of Alzheimer'S Disease : JAD|December 4, 2003
Apolipoprotein E and mortality in African-Americans and YorubaKathleen A Lane, Sujuan Gao, Siu L Hui, et al.Journal of the Neurological Sciences|July 20, 2002
P301L tauopathy: confocal immunofluorescence study of perinuclear aggregation of the mutated proteinEmil Adamec, Jill R Murrell, Masaki Takao, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 24, 2002
Genetic variation in apolipoprotein D affects the risk of Alzheimer disease in African-AmericansPurnima P Desai, Hugh C Hendrie, Rebecca M Evans, et al.Brain Pathology (Zurich, Switzerland)|March 26, 2011
Encephalopathy with neuroserpin inclusion bodies presenting as progressive myoclonus epilepsy and associated with a novel mutation in the Proteinase Inhibitor 12 geneMatthew C Hagen, Jill R Murrell, Marie-Bernadette Delisle, et al.Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 2010
Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron diseaseAlberto J Espay, Salvatore Spina, David J Houghton, et al.Acta Neuropathologica|June 28, 2005
Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein geneKeiji Yamaguchi, Elizabeth J Cochran, Jill R Murrell, et al.Pageof 8