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Journal of the Peripheral Nervous System : JPNS|June 27, 2015
MFN2 deletion of exons 7 and 8: founder mutation in the UK populationAisling S Carr, James M Polke, Jacob Wilson, et al.
Brain : a Journal of Neurology|March 14, 2024
Whole genome sequencing increases the diagnostic rate in Charcot-Marie-Tooth diseaseChristopher J Record, Menelaos Pipis, Mariola Skorupinska, et al.
International Journal of Molecular Sciences|November 27, 2024
Synovial Fluid Immune Cell Composition Following Intraarticular Fracture May Contribute to Posttraumatic OsteoarthritisAlexandra Hunter Aitchison, Nicholas B Allen, Conor N O'Neill, et al.
Neurology|October 22, 2020
Neurofilament Light Chain as a Biomarker of Hereditary Transthyretin-Mediated AmyloidosisSimina Ticau, Gautham V Sridharan, Shira Tsour, et al.
Frontiers in Immunology|February 14, 2024
<i>Tlr5</i> deficiency exacerbates lupus-like disease in the MRL/<i>lpr</i> mouse modelRazan M Alajoleen, David N Oakland, Rana Estaleen, et al.
Neurology|March 12, 2017
Mutations in noncoding regions of <i>GJB1</i> are a major cause of X-linked CMTPedro J Tomaselli, Alexander M Rossor, Alejandro Horga, et al.
JAMA Surgery|November 21, 2019
Long-term Functional, Psychological, Emotional, and Social Outcomes in Survivors of Firearm InjuriesMichael A Vella, Alexander Warshauer, Gabriella Tortorello, et al.
European Journal of Pharmacology|April 14, 2010
In vivo efficacy of acyl CoA: diacylglycerol acyltransferase (DGAT) 1 inhibition in rodent models of postprandial hyperlipidemiaAndrew J King, Jason A Segreti, Kelly J Larson, et al.
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