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P Parchi

Showing results (31-40 of 74) with videos related to

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Italian Journal of Neurological Sciences|October 1, 1992
Autonomic nervous system function in myotonic dystrophyG Pierangeli, A Lugaresi, M Contin, et al.
The Journal of Biological Chemistry|August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseasesS G Chen, D B Teplow, P Parchi, et al.
The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS|May 16, 2012
An optimal design for patient-specific templates for pedicle spine screws placementV Ferrari, P Parchi, S Condino, et al.
BMC Medical Genomics|February 11, 2022
Identification of recurrent genetic patterns from targeted sequencing panels with advanced data science: a case-study on sporadic and genetic neurodegenerative diseasesM Tarozzi, A Bartoletti-Stella, D Dall'Olio, 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 brainS Capellari, P Parchi, C M Russo, et al.
Acta Neurologica Scandinavica|January 4, 2012
Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L familyS N Popova, I Tarvainen, S Capellari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2009
'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2C La Morgia, P Parchi, S Capellari, et al.
Neurology|July 23, 1998
Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one caseI Ghorayeb, C Series, P Parchi, et al.
Neurology|March 9, 2005
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein geneS Capellari, F Cardone, S Notari, et al.
European Journal of Neurology|July 10, 2018
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrheaG Bommarito, M Cellerino, V Prada, et al.
Pageof 8

Showing results (31-40 of 74) with videos related to

Sort By:
Pageof 8
Italian Journal of Neurological Sciences|October 1, 1992
Autonomic nervous system function in myotonic dystrophyG Pierangeli, A Lugaresi, M Contin, et al.
The Journal of Biological Chemistry|August 11, 1995
Truncated forms of the human prion protein in normal brain and in prion diseasesS G Chen, D B Teplow, P Parchi, et al.
The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS|May 16, 2012
An optimal design for patient-specific templates for pedicle spine screws placementV Ferrari, P Parchi, S Condino, et al.
BMC Medical Genomics|February 11, 2022
Identification of recurrent genetic patterns from targeted sequencing panels with advanced data science: a case-study on sporadic and genetic neurodegenerative diseasesM Tarozzi, A Bartoletti-Stella, D Dall'Olio, 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 brainS Capellari, P Parchi, C M Russo, et al.
Acta Neurologica Scandinavica|January 4, 2012
Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L familyS N Popova, I Tarvainen, S Capellari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 20, 2009
'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2C La Morgia, P Parchi, S Capellari, et al.
Neurology|July 23, 1998
Creutzfeldt-Jakob disease with long duration and panencephalopathic lesions: molecular analysis of one caseI Ghorayeb, C Series, P Parchi, et al.
Neurology|March 9, 2005
Creutzfeldt-Jakob disease associated with the R208H mutation in the prion protein geneS Capellari, F Cardone, S Notari, et al.
European Journal of Neurology|July 10, 2018
A novel prion protein gene-truncating mutation causing autonomic neuropathy and diarrheaG Bommarito, M Cellerino, V Prada, et al.
Pageof 8