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BMJ Paediatrics Open|January 12, 2024
Vitamin D insufficiency in infants with increased risk of developing type 1 diabetes: a secondary analysis of the POInT StudyAn Jacobs, Maarten Warnants, Veronika Vollmuth, et al.
American Journal of Human Genetics|October 6, 2010
Mutations in the SPTLC2 subunit of serine palmitoyltransferase cause hereditary sensory and autonomic neuropathy type IAnnelies Rotthier, Michaela Auer-Grumbach, Katrien Janssens, et al.
Molecular and Cellular Neurosciences|September 6, 2005
Synaptopodin and 4 novel genes identified in primary sensory neuronsNathalie Verpoorten, Kristien Verhoeven, Stefan Weckx, et al.
Informatics for Health & Social Care|October 18, 2014
The OCareCloudS project: Toward organizing care through trusted cloud servicesFemke De Backere, Femke Ongenae, Frederic Vannieuwenborg, et al.
Nature Genetics|May 4, 2004
Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathyJoy Irobi, Katrien Van Impe, Pavel Seeman, et al.
Archives of Toxicology|December 13, 2016
Pan-European inter-laboratory studies on a panel of in vitro cytotoxicity and pro-inflammation assays for nanoparticlesJean-Pascal Piret, Olesja M Bondarenko, Matthew S P Boyles, et al.
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