Murray Grossman spends much of his time researching Pathology, Frontotemporal lobar degeneration, Dementia, Frontotemporal dementia and Amyotrophic lateral sclerosis. His work investigates the relationship between Frontotemporal lobar degeneration and topics such as Neuropathology that intersect with problems in Genetics, Single-nucleotide polymorphism and Genome-wide association study. The concepts of his Dementia study are interwoven with issues in Biomarker and Neuroscience.
His study on Semantic dementia is often connected to Inclusion bodies as part of broader study in Frontotemporal dementia. His Semantic dementia research incorporates elements of Primary progressive aphasia, Progressive nonfluent aphasia, Clinical psychology and Aphasia. His research investigates the connection between Amyotrophic lateral sclerosis and topics such as C9orf72 Protein that intersect with problems in UBQLN2.
Cognitive psychology, Frontotemporal dementia, Pathology, Frontotemporal lobar degeneration and Cognition are his primary areas of study. His Cognitive psychology study combines topics in areas such as Working memory, Semantic memory, Semantic dementia and Comprehension. Frontotemporal dementia is a subfield of Dementia that Murray Grossman studies.
His research integrates issues of Alzheimer's disease and Neuropsychology in his study of Dementia. His study explores the link between Pathology and topics such as White matter that cross with problems in Diffusion MRI. His work is dedicated to discovering how Frontotemporal lobar degeneration, Primary progressive aphasia are connected with Audiology and other disciplines.
His primary scientific interests are in Pathology, Frontotemporal dementia, Frontotemporal lobar degeneration, Disease and Atrophy. His research in Pathology focuses on subjects like White matter, which are connected to Diffusion MRI. Frontotemporal dementia is a primary field of his research addressed under Dementia.
He focuses mostly in the field of Dementia, narrowing it down to matters related to Cognition and, in some cases, Cognitive decline and Cognitive psychology. As a member of one scientific family, Murray Grossman mostly works in the field of Frontotemporal lobar degeneration, focusing on Progressive supranuclear palsy and, on occasion, Tauopathy. The study incorporates disciplines such as Primary progressive aphasia, Temporal lobe and Audiology in addition to Atrophy.
His main research concerns Pathology, Frontotemporal dementia, Frontotemporal lobar degeneration, Alzheimer's disease and Disease. His Pathology study deals with Biomarker intersecting with Retina. His Frontotemporal dementia study is focused on Internal medicine in general.
His work deals with themes such as Progressive supranuclear palsy, Neuropsychology, Memory span, C9orf72 and Likely pathogenic, which intersect with Frontotemporal lobar degeneration. In his work, Corticobasal degeneration, Beta, Fatty acid-binding protein and Immunology is strongly intertwined with Neurology, which is a subfield of Disease. His Primary progressive aphasia study incorporates themes from Comprehension, Audiology, Posterior cortical atrophy, Aphasia and Atrophy.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
Manuela Neumann;Deepak M. Sampathu;Linda K. Kwong;Adam C. Truax.
Classification of primary progressive aphasia and its variants
M L Gorno-Tempini;M L Gorno-Tempini;A E Hillis;S Weintraub;A Kertesz.
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia.
Katya Rascovsky;John R. Hodges;David Knopman;Mario F. Mendez.
Symmetric diffeomorphic image registration with cross-correlation: evaluating automated labeling of elderly and neurodegenerative brain.
Brian B. Avants;Charles L. Epstein;Murray Grossman;James C. Gee.
Medical Image Analysis (2008)
The neural basis of the central executive system of working memory.
Mark D'Esposito;John A. Detre;David C. Alsop;Robert K. Shin.
Clinical and Pathological Diagnosis of Frontotemporal Dementia: Report of the Work Group on Frontotemporal Dementia and Pick's Disease
Guy M. McKhann;Marilyn S. Albert;Murray Grossman;Bruce Miller.
JAMA Neurology (2001)
Criteria for the diagnosis of corticobasal degeneration
Melissa J. Armstrong;Irene Litvan;Anthony E. Lang;Thomas H. Bak.
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis
Vivianna M. Van Deerlin;James B. Leverenz;James B. Leverenz;Lynn M. Bekris;Thomas D. Bird;Thomas D. Bird.
Lancet Neurology (2008)
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Günter U Höglinger;Gesine Respondek;Maria Stamelou;Carolin Kurz.
Movement Disorders (2017)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli;Brittany N Lasseigne;Slave Petrovski;Peter C Sapp.
Profile was last updated on December 6th, 2021.
Research.com Ranking is based on data retrieved from the Microsoft Academic Graph (MAG).
The ranking d-index is inferred from publications deemed to belong to the considered discipline.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: