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S Capellari

Showing results (21-30 of 54) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphologyC Jansen, J C van Swieten, S Capellari, 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|January 5, 2002
Inherited prion disease caused by the V210I mutation: transmission to transgenic miceJ A Mastrianni, S Capellari, G C Telling, 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.
Neurology|November 27, 2002
Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein geneS Capellari, P Parchi, B D Wolff, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Inherited Creutzfeldt-Jakob disease in a Dutch patient with a novel five octapeptide repeat insertion and unusual cerebellar morphologyC Jansen, J C van Swieten, S Capellari, 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|January 5, 2002
Inherited prion disease caused by the V210I mutation: transmission to transgenic miceJ A Mastrianni, S Capellari, G C Telling, 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.
Neurology|November 27, 2002
Creutzfeldt-Jakob disease associated with a deletion of two repeats in the prion protein geneS Capellari, P Parchi, B D Wolff, et al.
Pageof 6