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European Journal of Neurology|August 8, 2009
Revascularization in acute ischaemic stroke using the penumbra system: the first single center experienceI Q Grunwald, S Walter, P Papanagiotou, et al.
Prenatal Diagnosis|July 8, 2025
Open Spinal Dysraphism Without Hindbrain Herniation-Natural History and Postnatal OutcomeI Bedei, C C Kik, R Axt-Fliedner, et al.
American Journal of Human Genetics|May 11, 2006
Mutations in the gene encoding peroxisomal sterol carrier protein X (SCPx) cause leukencephalopathy with dystonia and motor neuropathyS Ferdinandusse, P Kostopoulos, S Denis, et al.
ACS Medicinal Chemistry Letters|February 19, 2025
Heterocyclic Assembly: An Underutilized Disconnection with Potential to Maximize High Fsp3 Chemical Space ExplorationBrandon M Taoka, Ning Qi, Zachary G Brill, et al.
Molecular and Cellular Biology|May 4, 2004
The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specificationE Bonnafe, M Touka, A AitLounis, et al.
Human Molecular Genetics|May 23, 1998
Genetic and molecular definition of complementation group D in MHC class II deficiencyM C Fondaneche, J Villard, W Wiszniewski, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 11, 2010
Gene delivery of TGF-β1 induces arthrofibrosis and chondrometaplasia of synovium in vivoRachael S Watson, Elvire Gouze, Padraic P Levings, et al.
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