Her primary scientific interests are in Pathology, Alzheimer's disease, Dementia, Neuroscience and Frontotemporal dementia. The concepts of her Alzheimer's disease study are interwoven with issues in Dementia with Lewy bodies and Neuroimaging. Her Dementia with Lewy bodies study incorporates themes from Neurocognitive, Psychiatry, Clinical trial and REM sleep behavior disorder.
Her research integrates issues of Bioinformatics, Unified Parkinson's disease rating scale, Occipital lobe, Tauopathy and Amyloid in her study of Dementia. Her work carried out in the field of Neuroscience brings together such families of science as Corticobasal degeneration, Behavior disorder, Physical medicine and rehabilitation and Alternative splicing. Her Frontotemporal dementia research incorporates elements of Genetics and Amyotrophic lateral sclerosis.
Melissa E. Murray spends much of her time researching Pathology, Disease, Dementia, Alzheimer's disease and Neuroscience. Her biological study spans a wide range of topics, including Hippocampal formation, Cognition and Neuroimaging. Many of her research projects under Dementia are closely connected to Hippocampal sclerosis with Hippocampal sclerosis, tying the diverse disciplines of science together.
Her study looks at the relationship between Frontotemporal dementia and topics such as Amyotrophic lateral sclerosis, which overlap with Frontotemporal lobar degeneration. Melissa E. Murray works mostly in the field of Alzheimer's disease, limiting it down to topics relating to Apolipoprotein E and, in certain cases, Oncology. Her study looks at the intersection of Neuroscience and topics like Tauopathy with Corticobasal degeneration and Tau protein.
Her primary scientific interests are in Disease, Pathology, Neuropathology, Dementia and Neuroscience. Her work in Disease addresses subjects such as Biomarker, which are connected to disciplines such as Clinical trial. Her Pathology research is multidisciplinary, incorporating perspectives in Hippocampal formation, Hippocampus and Entorhinal cortex.
Her Neuropathology study combines topics in areas such as Genome-wide association study, Parkinsonism, Cognitive decline, Alzheimer's disease and Haplotype. Her study in Dementia is interdisciplinary in nature, drawing from both Pathological and Cognition. Her work deals with themes such as Gene expression and Neurodegeneration, which intersect with Neuroscience.
Melissa E. Murray mainly focuses on Pathology, Disease, Neuropathology, Alzheimer's disease and Entorhinal cortex. Pathology and Hippocampus are commonly linked in her work. Disease is closely attributed to Odds ratio in her study.
Her Alzheimer's disease research is multidisciplinary, incorporating elements of Dementia with Lewy bodies and Cohort. Her studies in Entorhinal cortex integrate themes in fields like Percentile, Cognition, Effects of sleep deprivation on cognitive performance and Audiology. Her research in Tauopathy intersects with topics in Hippocampal formation, Encephalopathy, Frontotemporal dementia and Bioinformatics.
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Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium
Ian G. McKeith;Bradley F. Boeve;Dennis W. DIckson;Glenda Halliday.
Primary age-related tauopathy (PART): a common pathology associated with human aging
John F. Crary;John Q. Trojanowski;Julie A. Schneider;Jose F. Abisambra.
Acta Neuropathologica (2014)
Neuropathologically defined subtypes of Alzheimer's disease with distinct clinical characteristics: a retrospective study.
Melissa E Murray;Neill R Graff-Radford;Owen A Ross;Ronald C Petersen.
Lancet Neurology (2011)
Limbic-predominant age-related TDP-43 encephalopathy (LATE): consensus working group report.
Peter T. Nelson;Dennis W. Dickson;John Q. Trojanowski;Clifford R. Jack.
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics
Ian R. Mackenzie;Alexandra M. Nicholson;Mohona Sarkar;James Messing.
MRI correlates of neurofibrillary tangle pathology at autopsy: a voxel-based morphometry study.
J. L. Whitwell;K. A. Josephs;M. E. Murray;K. Kantarci.
Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72
Bradley F. Boeve;Kevin B. Boylan;Neill R. Graff-Radford;Mariely DeJesus-Hernandez.
An autoradiographic evaluation of AV-1451 Tau PET in dementia.
Val J. Lowe;Geoffry Curran;Ping Fang;Amanda M. Liesinger.
Acta neuropathologica communications (2016)
Neuroimaging correlates of pathologically defined subtypes of Alzheimer's disease: a case-control study
Jennifer L Whitwell;Dennis W Dickson;Melissa E Murray;Stephen D Weigand.
Lancet Neurology (2012)
C9ORF72 repeat expansions in mice cause TDP-43 pathology, neuronal loss, and behavioral deficits
Jeannie Chew;Tania F. Gendron;Mercedes Prudencio;Hiroki Sasaguri.
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