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Annals of Neurology
|
January 1, 1991
Acceleration of scrapie in trisomy 16----diploid aggregation chimeras
C J Epstein, D B Foster, S J DeArmond, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1981
Glial fibrillary acidic protein in hepatic encephalopathy. An immunohistochemical study
R A Sobel, S J DeArmond, L S Forno, et al.
Journal of Neuroimmunology
|
March 1, 1981
Post-embedding immunoperoxidase staining of glial fibrillary acidic protein for light and electron microscopy
S J DeArmond, M W Siegel, R G Dixon, et al.
Journal of Neurochemistry
|
December 1, 1986
Turnover of glial filaments in mouse spinal cord
S J DeArmond, Y L Lee, H A Kretzschmar, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
March 29, 1994
Genetics of prion diseases and prion diversity in mice
G A Carlson, S J DeArmond, M Torchia, et al.
Journal of Neuropathology and Experimental Neurology
|
December 22, 1999
Kinetics of prion protein accumulation in the CNS of mice with experimental scrapie
J Tatzelt, D F Groth, M Torchia, et al.
Acta Neuropathologica
|
January 1, 1989
Sulfated glycosaminoglycans in amyloid plaques of prion diseases
A D Snow, R Kisilevsky, J Willmer, et al.
Journal of Neurosurgery
|
April 1, 1986
The proliferative potential of human pituitary tumors in situ
T Nagashima, J A Murovic, T Hoshino, et al.
Brain Research
|
August 29, 2000
Selective neuronal vulnerability during experimental scrapie infection: insights from an ultrastructural investigation
E Bouzamondo, A M Milroy, H J Ralston, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 5, 1997
Isolated myoclonic alien hand as the sole presentation of pathologically established Creutzfeldt-Jakob disease: a report of two patients
D J MacGowan, N Delanty, F Petito, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 123) with videos related to
Sort By:
Page
of 13
Annals of Neurology
|
January 1, 1991
Acceleration of scrapie in trisomy 16----diploid aggregation chimeras
C J Epstein, D B Foster, S J DeArmond, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1981
Glial fibrillary acidic protein in hepatic encephalopathy. An immunohistochemical study
R A Sobel, S J DeArmond, L S Forno, et al.
Journal of Neuroimmunology
|
March 1, 1981
Post-embedding immunoperoxidase staining of glial fibrillary acidic protein for light and electron microscopy
S J DeArmond, M W Siegel, R G Dixon, et al.
Journal of Neurochemistry
|
December 1, 1986
Turnover of glial filaments in mouse spinal cord
S J DeArmond, Y L Lee, H A Kretzschmar, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
March 29, 1994
Genetics of prion diseases and prion diversity in mice
G A Carlson, S J DeArmond, M Torchia, et al.
Journal of Neuropathology and Experimental Neurology
|
December 22, 1999
Kinetics of prion protein accumulation in the CNS of mice with experimental scrapie
J Tatzelt, D F Groth, M Torchia, et al.
Acta Neuropathologica
|
January 1, 1989
Sulfated glycosaminoglycans in amyloid plaques of prion diseases
A D Snow, R Kisilevsky, J Willmer, et al.
Journal of Neurosurgery
|
April 1, 1986
The proliferative potential of human pituitary tumors in situ
T Nagashima, J A Murovic, T Hoshino, et al.
Brain Research
|
August 29, 2000
Selective neuronal vulnerability during experimental scrapie infection: insights from an ultrastructural investigation
E Bouzamondo, A M Milroy, H J Ralston, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 5, 1997
Isolated myoclonic alien hand as the sole presentation of pathologically established Creutzfeldt-Jakob disease: a report of two patients
D J MacGowan, N Delanty, F Petito, et al.
Page
of 13