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Casper Jansen

Showing results (1-10 of 23) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|September 30, 2009
[Human spongiform encephalopathies in the Netherlands]Maaike Schuur, Casper Jansen, Annemieke J M Rozemuller, et al.
Acta Neuropathologica Communications|February 21, 2018
Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion proteinBrent Race, Katie Williams, Andrew G Hughson, et al.
Journal of Neurology|December 19, 2023
Primary central nervous system lymphomaMyrthe E de Koning, Jurrit J Hof, Casper Jansen, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 30, 2009
[Eleven years of autopsy on account of Creutzfeldt-Jakob disease in the Netherlands]Casper Jansen, Maaike Schuur, Wim G M Spliet, et al.
Journal of Neuropathology and Experimental Neurology|July 16, 2011
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patientCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Prion|August 17, 2012
Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob diseaseJolanta Bratosiewicz-Wąsik, Joanna Smoleń-Dzirba, Annemieke J Rozemuller, et al.
Neuro-Degenerative Diseases|March 9, 2012
Neuroinflammation and common mechanism in Alzheimer's disease and prion amyloidosis: amyloid-associated proteins, neuroinflammation and neurofibrillary degenerationAnnemieke J M Rozemuller, Casper Jansen, Anna Carrano, et al.
Folia Neuropathologica|April 17, 2012
Association of the PRNP regulatory region polymorphisms with the occurrence of sporadic Creutzfeldt-Jakob diseaseJolanta Bratosiewicz-Wąsik, Joanna Smoleń-Dzirba, Cezary Watała, et al.
Resuscitation|December 19, 2018
Postmortem histopathology of electroencephalography and evoked potentials in postanoxic comaMichel J A M van Putten, Casper Jansen, Marleen C Tjepkema-Cloostermans, et al.
Acta Neuropathologica|November 14, 2009
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNPCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Nederlands Tijdschrift Voor Geneeskunde|September 30, 2009
[Human spongiform encephalopathies in the Netherlands]Maaike Schuur, Casper Jansen, Annemieke J M Rozemuller, et al.
Acta Neuropathologica Communications|February 21, 2018
Familial human prion diseases associated with prion protein mutations Y226X and G131V are transmissible to transgenic mice expressing human prion proteinBrent Race, Katie Williams, Andrew G Hughson, et al.
Journal of Neurology|December 19, 2023
Primary central nervous system lymphomaMyrthe E de Koning, Jurrit J Hof, Casper Jansen, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 30, 2009
[Eleven years of autopsy on account of Creutzfeldt-Jakob disease in the Netherlands]Casper Jansen, Maaike Schuur, Wim G M Spliet, et al.
Journal of Neuropathology and Experimental Neurology|July 16, 2011
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patientCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Prion|August 17, 2012
Association between the PRNP 1368 polymorphism and the occurrence of sporadic Creutzfeldt-Jakob diseaseJolanta Bratosiewicz-Wąsik, Joanna Smoleń-Dzirba, Annemieke J Rozemuller, et al.
Neuro-Degenerative Diseases|March 9, 2012
Neuroinflammation and common mechanism in Alzheimer's disease and prion amyloidosis: amyloid-associated proteins, neuroinflammation and neurofibrillary degenerationAnnemieke J M Rozemuller, Casper Jansen, Anna Carrano, et al.
Folia Neuropathologica|April 17, 2012
Association of the PRNP regulatory region polymorphisms with the occurrence of sporadic Creutzfeldt-Jakob diseaseJolanta Bratosiewicz-Wąsik, Joanna Smoleń-Dzirba, Cezary Watała, et al.
Resuscitation|December 19, 2018
Postmortem histopathology of electroencephalography and evoked potentials in postanoxic comaMichel J A M van Putten, Casper Jansen, Marleen C Tjepkema-Cloostermans, et al.
Acta Neuropathologica|November 14, 2009
Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNPCasper Jansen, Piero Parchi, Sabina Capellari, et al.
Pageof 3