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Parkinsonism & Related Disorders|August 23, 2011
The relation between depression and parkin genotype: the CORE-PD studyA Srivastava, M-X Tang, H Mejia-Santana, et al.
The Journal of Experimental Medicine|March 20, 2002
Progress toward a human CD4/CCR5 transgenic rat model for de novo infection by human immunodeficiency virus type 1Oliver T Keppler, Frank J Welte, Tuan A Ngo, et al.
Neurology|March 24, 2012
Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD studyR N Alcalay, E Caccappolo, H Mejia-Santana, et al.
The Journal of Clinical Investigation|February 16, 2008
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathyJoachim Schessl, Yaqun Zou, Meagan J McGrath, et al.
Brain : a Journal of Neurology|February 3, 2009
Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1Joachim Schessl, Ana L Taratuto, Caroline Sewry, et al.
Neurology|April 5, 2015
Challenges and opportunities in designing clinical trials for neuromyelitis opticaBrian G Weinshenker, Gerard Barron, Jacinta M Behne, et al.
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