Search research articles
Contact Us
Filters
Showing results (121-130 of 203) with videos related to
Page
of 21
Sort By:
The Journal of Biological Chemistry
|
November 14, 1997
Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutation
N Singh, G Zanusso, S G Chen, et al.
Neurology
|
April 1, 1996
Fatal familial insomnia: behavioral and cognitive features
R Gallassi, A Morreale, P Montagna, et al.
The Journal of Biological Chemistry
|
August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseases
S G Chen, D B Teplow, P Parchi, et al.
The American Journal of Pathology
|
August 10, 2000
Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain
S Capellari, P Parchi, C M Russo, et al.
Electroencephalography and Clinical Neurophysiology
|
June 1, 1992
Abnormal sympathetic skin responses in thalamic lesions
P Montagna, P Cortelli, P Avoni, et al.
Brain Research
|
October 27, 1987
Carbon disulfide axonopathy. Another experimental model characterized by acceleration of neurofilament transport and distinct changes of axonal size
M Pappolla, R Penton, H S Weiss, et al.
Neurology
|
March 1, 1992
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178
R Medori, P Montagna, H J Tritschler, et al.
British Medical Bulletin
|
October 1, 1993
Fatal familial insomnia and the widening spectrum of prion diseases
P Gambetti, R Petersen, L Monari, et al.
The Journal of Biological Chemistry
|
August 7, 1999
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein
G Zanusso, R B Petersen, T Jin, et al.
Electroencephalography and Clinical Neurophysiology
|
June 1, 1995
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation
E Sforza, P Montagna, P Tinuper, et al.
Page
of 21
Search research articles
Search
Showing results (121-130 of 203) with videos related to
Sort By:
Page
of 21
The Journal of Biological Chemistry
|
November 14, 1997
Prion protein aggregation reverted by low temperature in transfected cells carrying a prion protein gene mutation
N Singh, G Zanusso, S G Chen, et al.
Neurology
|
April 1, 1996
Fatal familial insomnia: behavioral and cognitive features
R Gallassi, A Morreale, P Montagna, et al.
The Journal of Biological Chemistry
|
August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseases
S G Chen, D B Teplow, P Parchi, et al.
The American Journal of Pathology
|
August 10, 2000
Effect of the E200K mutation on prion protein metabolism. Comparative study of a cell model and human brain
S Capellari, P Parchi, C M Russo, et al.
Electroencephalography and Clinical Neurophysiology
|
June 1, 1992
Abnormal sympathetic skin responses in thalamic lesions
P Montagna, P Cortelli, P Avoni, et al.
Brain Research
|
October 27, 1987
Carbon disulfide axonopathy. Another experimental model characterized by acceleration of neurofilament transport and distinct changes of axonal size
M Pappolla, R Penton, H S Weiss, et al.
Neurology
|
March 1, 1992
Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178
R Medori, P Montagna, H J Tritschler, et al.
British Medical Bulletin
|
October 1, 1993
Fatal familial insomnia and the widening spectrum of prion diseases
P Gambetti, R Petersen, L Monari, et al.
The Journal of Biological Chemistry
|
August 7, 1999
Proteasomal degradation and N-terminal protease resistance of the codon 145 mutant prion protein
G Zanusso, R B Petersen, T Jin, et al.
Electroencephalography and Clinical Neurophysiology
|
June 1, 1995
Sleep-wake cycle abnormalities in fatal familial insomnia. Evidence of the role of the thalamus in sleep regulation
E Sforza, P Montagna, P Tinuper, et al.
Page
of 21