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Neuroimage|January 5, 2010
Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutationsJonathan D Rohrer, Gerard R Ridgway, Marc Modat, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 30, 2026
A scalable, dividing cell model for the robust propagation and quantification of human sporadic Creutzfeldt-Jakob disease prionsAkin Nihat, Parineeta Arora, Christian Schmidt, et al.
Human Molecular Genetics|May 17, 2014
In vitro screen of prion disease susceptibility genes using the scrapie cell assayCraig A Brown, Christian Schmidt, Mark Poulter, et al.
The Journal of Allergy and Clinical Immunology|August 28, 2016
Pulmonary sarcoidosis is associated with exosomal vitamin D-binding protein and inflammatory moleculesMaria-Jose Martinez-Bravo, Casper J E Wahlund, Khaleda Rahman Qazi, et al.
Journal of Neurology|March 10, 2011
A novel exon 2 I27V VCP variant is associated with dissimilar clinical syndromesJonathan D Rohrer, Jason D Warren, David Reiman, et al.
European Journal of Human Genetics : EJHG|April 10, 2014
Predictive testing for inherited prion disease: report of 22 years experienceJane Owen, Jon Beck, Tracy Campbell, et al.
JAMA Neurology|November 17, 2015
Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological CorrelationLaura Eisenmenger, Marie-Claire Porter, Christopher J Carswell, et al.
Cells|December 24, 2021
NT1-Tau Is Increased in CSF and Plasma of CJD Patients, and Correlates with Disease ProgressionDavid Mengel, Tze How Mok, Akin Nihat, et al.
Methods in Molecular Biology (Clifton, N.J.)|September 2, 2017
Methods for Molecular Diagnosis of Human Prion DiseaseJonathan D F Wadsworth, Gary Adamson, Susan Joiner, et al.
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