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European Journal of Human Genetics : EJHG|March 14, 2008
In tandem analysis of CLCN1 and SCN4A greatly enhances mutation detection in families with non-dystrophic myotoniaJeroen Trip, Gea Drost, Dennis J Verbove, et al.
International Journal of Molecular Sciences|November 26, 2022
Peripheral Ion Channel Genes Screening in Painful Small Fiber NeuropathyMilena Ślęczkowska, Rowida Almomani, Margherita Marchi, et al.
Experimental Neurology|October 15, 2018
Expression of pathogenic SCN9A mutations in the zebrafish: A model to study small-fiber neuropathyIvo Eijkenboom, Maurice Sopacua, Auke B C Otten, et al.
BMC Medicine|March 19, 2026
Characterizing the effects of genetic liability to autoimmune conditions on pregnancy outcomes using Mendelian randomizationElisabeth Aiton, Nancy S McBride, Gemma L Clayton, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 13, 2024
Femoral neck width genetic risk score is a novel independent risk factor for hip fracturesJonathan H Tobias, Maria Nethander, Benjamin G Faber, et al.
British Journal of Anaesthesia|August 16, 2012
Pain relief and quality-of-life improvement after spinal cord stimulation in painful diabetic polyneuropathy: a pilot studyW A Pluijms, R Slangen, M Bakkers, et al.
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