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P Parchi

Showing results (61-70 of 74) with videos related to

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Brain Pathology (Zurich, Switzerland)|July 21, 1998
Neuronal apoptosis in fatal familial insomniaA Dorandeu, L Wingertsmann, F Chrétien, et al.
Journal of Biological Regulators and Homeostatic Agents|December 1, 2017
Complications and survival of megaprostheses after resection of bone metastasesM De Gori, A D’Arienzo, L Andreani, et al.
Neurology|April 22, 2009
Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob diseaseD N Manners, P Parchi, C Tonon, et al.
European Journal of Neurology|September 11, 2002
A French cluster of Creutzfeldt-Jakob disease: a molecular analysisP Beaudry, P Parchi, K Peoc'h, et al.
Archives of Neurology|October 27, 2001
Creutzfeldt-Jakob disease in unusually young patients who consumed venisonE D Belay, P Gambetti, L B Schonberger, et al.
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker diseaseP Parchi, S G Chen, P Brown, et al.
Neuropathology and Applied Neurobiology|September 30, 2010
The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau depositsC Jansen, P Parchi, B Jelles, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Brain Pathology (Zurich, Switzerland)|July 21, 1998
Neuronal apoptosis in fatal familial insomniaA Dorandeu, L Wingertsmann, F Chrétien, et al.
Journal of Biological Regulators and Homeostatic Agents|December 1, 2017
Complications and survival of megaprostheses after resection of bone metastasesM De Gori, A D’Arienzo, L Andreani, et al.
Neurology|April 22, 2009
Pathologic correlates of diffusion MRI changes in Creutzfeldt-Jakob diseaseD N Manners, P Parchi, C Tonon, et al.
European Journal of Neurology|September 11, 2002
A French cluster of Creutzfeldt-Jakob disease: a molecular analysisP Beaudry, P Parchi, K Peoc'h, et al.
Archives of Neurology|October 27, 2001
Creutzfeldt-Jakob disease in unusually young patients who consumed venisonE D Belay, P Gambetti, L B Schonberger, et al.
Annals of Neurology|June 1, 1996
Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob diseaseP Parchi, R Castellani, S Capellari, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1998
Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker diseaseP Parchi, S G Chen, P Brown, et al.
Neuropathology and Applied Neurobiology|September 30, 2010
The first case of fatal familial insomnia (FFI) in the Netherlands: a patient from Egyptian descent with concurrent four repeat tau depositsC Jansen, P Parchi, B Jelles, et al.
Nature Medicine|September 1, 1997
Allelic origin of the abnormal prion protein isoform in familial prion diseasesS G Chen, P Parchi, P Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 2000
Genetic influence on the structural variations of the abnormal prion proteinP Parchi, W Zou, W Wang, et al.
Pageof 8