S. J. DeArmond - Concepedia

Author

S. J. DeArmond

Also Known As

S Dearmond, S J DeArmond, S J Dearmond, S. DeArmond, S. J. DeArmond, S. J. Dearmond, S.J DeArmond, S.J. DeArmond, SJ DeArmond, Stephen J. DeArmond

Publications

8.2K

Citations

H-Index

103

Concepts

All Affiliations

University of California, San Francisco University Memory and Aging Center Neurological Surgery

About

S. J. DeArmond is an author at University of California, San Francisco specializing in medicine, neurology, and proteomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	30	4.2K
2	Natural Sciences	12	12	1.7K
3	Social Sciences	7	7	1.2K
4	Biochemistry	6	6	322
5	Health Sciences	4	4	438

S. J. DeArmond

Publications

7.7K

Citations

H-Index

Page 1

	Year	Citations
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies. Stanley B. Prusiner, Darlene Groth, Ana Serban, Proceedings of the National Academy of Sciences GeneticsMolecular BiologyProtein ExpressionExperimental NeuropathologyPrion Disease	1993	465
Scrapie prion proteins are synthesized in neurons. H. A. Kretzschmar, Stanley B. Prusiner, Linda Stowring, PubMed	1986	425
Regional mapping of prion proteins in brain. Albert Taraboulos, K. Jendroska, D. Serban, Proceedings of the National Academy of Sciences Prion Protein PrpscMolecular NeuroscienceCreutzfeldt-jakob DiseaseMedicineHistopathology	1992	326
Amyloid vs FDG-PET in the differential diagnosis of AD and FTLD G.D. Rabinovici, Howard J. Rosen, Adi Alkalay, Neurology	2011	322
Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein. Glenn C. Telling, Michael Scott, Karen Hsiao, Proceedings of the National Academy of Sciences Creutzfeldt-jakob DiseaseTransgenic Mouse ModelsGeneticsImmunologyChimeric Prp	1994	310
Diagnostic Criteria for Sporadic Creutzfeldt-Jakob Disease H. A. Kretzschmar, James W. Ironside, S. J. DeArmond, Archives of Neurology	1996	287
Serial transmission in rodents of neurodegeneration from transgenic mice expressing mutant prion protein. Karen Hsiao, Darlene Groth, Michael Scott, Proceedings of the National Academy of Sciences Creutzfeldt-jakob DiseaseTransgenic Mouse ModelsSynaptic TransmissionGeneticsImmunology	1994	282
A hypothalamic neuronal cell line persistently infected with scrapie prions exhibits apoptosis Hermann Schätzl, Lajos László, David M. Holtzman, Journal of Virology Creutzfeldt-jakob DiseaseCell DeathExperimental NeuropathologyDegenerative PathologyPrion Disease	1997	276
Changes in the localization of brain prion proteins during scrapie infection S. J. DeArmond, William C. Mobley, D. L. DeMott, Neurology	1987	268
Distinct MRI Atrophy Patterns in Autopsy-Proven Alzheimer's Disease and Frontotemporal Lobar Degeneration Gil D. Rabinovici, William W. Seeley, E. J. Kim, American Journal of Alzheimer s Disease & Other Dementias®	2007	262

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